Zum Inhalt

Application of DSP2 for biological sex estimation in a Spanish sample: analysis based on sex and side

  • Open Access
  • 15.11.2024
  • Original Article
Erschienen in:

Abstract

Applying existing sexing methodologies to different populations, and reporting these findings is important to enhance their applicability and accuracy in real cases across the world. DSP was published in 2005 (Murail et al., 2005) and updated as a DSP2 in 2017 (Brůžek et al., 2017) based on a database of 10 pelvic measurements from 2040 individuals worldwide. These tools have been applied subsequently to various populations, however, its applicability to a dry Spanish population is lacking. 303 hipbones belonging to 157 individuals from the School of Legal Medicine from the University Complutense of Madrid (Spain), of which 140 individuals were documented, were analyzed to investigate the reliability, applicability and accuracy of the DSP2 sex estimation methodology, examining side and sex-based potential differences for the first time. In most of the DSP variables, intra-rater reliability showed excellent results and % applicability was higher than 85.0%. Overall % accuracy was higher than 94.0% regardless of the number or discriminant power of the utilized DSP variables. However, % sexing decreased when less variables or less discriminant ones were used for estimations, reaching 45.51% (left) and 43.31% (right). Regarding sexual dimorphism, females’ results of % applicability, % sexing and % accuracy were higher compared to males. In addition, left os coxae achieved better outcomes (aforementioned percentages) in most of the cases in the sex-pooled sample. Decreasing the mandatory posterior probability by 10% yielded an increase in the % sexing but reduced % accuracy, and thus, does not seem to enhance the approach’s performance. The present study validates the applicability and reliability of DSP for sexing a Spanish population. Future investigations will attempt to assess its applicability within virtual anthropology.

Supplementary Information

The online version contains supplementary material available at https://doi.org/10.1007/s00414-024-03358-1.

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Introduction

Estimating the sex of adult skeletal remains is a critical step in the reconstruction of anthropological profiles, and by extension, human identification, particularly in medico-legal or osteo-archaeological contexts. Despite numerous anatomical elements within the skeletal framework that have been utilised for deriving sexing models [1], the skull and pelvis have demonstrated a greater predominance for sex estimation across literature [25]. Between these two markers, the direct relationship of the pelvis with biological sex, attributable to its active role in parturition, renders pelvic characteristics more accurate for sexing, in comparison to cranial parameters [6]. Although some enriching approaches have exhaustively described sexing variables using graphic explanations and introduced greater objectivity through score-based approaches [7], these visual or morphognostic techniques, compared to metric ones, continue to remain problematic. Visual techniques, in addition to generally being highly subjective, which results in higher intra-inter-observer errors, warrant prior experience to be able to apply them accurately [7]. Morphometric techniques, on the other hand, are more objective, repeatable, and verifiable, which have led researchers to prefer them over the former [8, 9].
Murail and colleagues developed a new morphometric technique (DSP: Diagnose Sexuelle Probabiliste = Probabilistic Sex Diagnosis) in 2005 [10] to estimate the sex of skeletal remains using ten pelvic measurements and obtained an overall accuracy value of 99.63%. This methodology was originally created based on a worldwide reference sample of 2040 individuals from Europe (France, England, Portugal and Lithuania), Africa (South Africa), North America (United States of America) and Asia (Thailand). In addition to this geographical diversity, different ethnic groups (Zulu, Soto, Afrikaner, African American, and European American) and temporal periods (from 18th to late 20th centuries) were also considered within the analyses to reinforce its potential applicability in miscellaneous populations. In 2017, a freely available updated software, the DSP2, was created and validated using two new samples from the Maxwell Museum Documented Collection (University of New Mexico, Albuquerque, United States) and the Simon Collection of identified skeletons (Department of Anthropology, University of Geneva, Switzerland) [11].
Since its publication, this pelvic-based ten-variable metric methodology has been tested in geographically diverse, documented collections with accuracy outcomes ranging from 88.34 to 100%: France [12], Greece [13], Mexico [14] and Brazil [1517]. This approach has also shown high reliability and accurate results with virtual/ digital samples, i.e., using CT images from Europe, specifically Belgium [18], France [19], and Denmark [20]. Furthermore, these proven advantages led to its application to past population samples from Neanderthals [21], Pre-Columbian mummies [22], Gravettian individuals [23], Joseon Dynasty Koreans [24] and medieval skeletal remains [25]. Although the original studies advocated for the existence of a common sexual pattern worldwide [10, 11], to the best of our knowledge, this is the first time the DSP approach is being tested in a Spanish documented collection.
This study aimed to (1) analyze the intra-rater reliability, applicability, and accuracy of the DSP2 method when applied to a Spanish documented collection for sex estimation; (2) examine and compare the % applicability, % sexing and % accuracy of DSP2 among sexes and sides; (3) investigate how the combination of utilized DSP2 variables and the posterior probability can change the accuracy outcomes and (4) compare the sexing and accuracy percentages reported across different populations.

Materials and methods

Sample

The sample used for this investigation is derived from the modern documented skeletal collection housed in the School of Legal Medicine at the Faculty of Medicine of the Complutense University of Madrid (Madrid, Spain) [26]. As of 2023 the collection includes 238 individuals and continues to expand due to the ongoing agreement between the University and the funeral services of the Community of Madrid. However, at the time of data acquisition (2010), this twentieth-century collection potentially included 195 accessible individuals (80 females and 115 males) ranging from 3 to 97 years of age.
During the analysis, only mature individuals with the three elements of the innominate fused were selected and remains displaying pelvic pathologies were excluded from the study. This yielded a study sample comprising of 157 individuals. Within this sample, preservation permitted applying the DSP2 methodology to at least one of the hipbones (left and/or right) of most individuals. However, seven right hipbones and four left ones did not have counterparts to undertake corresponding comparisons, attributable to either poor preservation, or total absence. Thus, the final tally of analyzed sample included 303 coxal bones obtained from 157 individuals.
Demographic information derived from obituary records (age-at-death and biological sex) was not available for all individuals. Hence, accuracy investigation, for which documented sex is critical, was undertaken with a reduced dataset of 140 os coxae (74 males [54.4%] and 66 females [45.6%]; Table 1). Within this subset, 136 individuals were fully documented (age-at-death and biological sex), and 4 were partially identified (3 males and 1 female; whose ages were unknown). Regarding sex-wise age distribution of this subset, the female subsample was significantly older than males (♀ 68.82 ± 16.26 years vs. ♂ 57.52 ± 19.47 years; Mann-Whitney U = 1566.5; p = 0.001), as is observed within osteological documented collections, attributable to differential life expectancy, amongst other factors.
Table 1
Demographic information about the documented sample from the University Complutense of Madrid used for the investigation of accuracy outcomes (N = 140)
Age group
Males
Females
Total
N
%
N
%
< 30 years old
04
5.4
01
1.5
06
30–39 years old
12
16.2
05
7.6
19
40–49 years old
11
14.9
04
6.1
16
50–59 years old
13
17.6
06
9.1
15
60–69 years old
05
6.8
10
15.2
19
70–79 years old
14
18.9
21
31.8
35
80–89 years old
10
13.5
16
24.2
25
> 90 years old
02
2.7
02
3.0
04
Unknown age
03
4.1
01
1.5
04
Total
74
100.0
66
100.0
140

Sex estimation

During the examination process, the innominate was separated from the rest of the skeleton to prevent complementary information from affecting the objectivity of the results. Thus, the sex estimation technique was applied blindly by the first author, without knowing any biological information for the individuals analyzed. Additionally, no other information that could affect the study (except for the individual’s code) was available where the material is stored.
The DSP tool, originally created and published to enable non-population specific sex estimation in 2005, utilised a simple spreadsheet program where the researcher could type in the maximum possible number of variables (measurements in mm) out of the recommended ten, with a required minimum of four variables. Based on the input data, the probability of each specimen being male or female was automatically computed, with an equal prior probability for male and female groups (pMale = pFemale = 0.5). It is important to highlight that although the program worked with a minimum of four variables, the more variables utilised for analysis, the greater was the likelihood of obtaining a significant probability. In addition, sex was determined only if the posterior probability was ≥ 0.95 threshold, which equates to a risk of error of 0.05 i.e., the maximum required for reliable palaeobiological studies [6]. If these probability and error conditions were not fulfilled, an individual was classified as undetermined. The ten measurements that the method employed were the following:
  • PUM - Acetabulo-symphyseal pubic length: minimum distance from the superior and medial point of the pubic symphysis to the nearest point on the acetabular rim at the level of the lunate surface [27].
  • SPU - Cotylo- pubic width: pubic breadth between the most lateral acetabular point and the medial aspect of the pubis. Measurement is perpendicular to the major axis of the os pubis; arms of the sliding caliper are thus parallel to the plane of the obturator foramen [28].
  • DCOX - Innominate or coxal length: maximum height of os coxae measured from the inferior border of the os coxae to the most superior portion of the iliac crest. Can be measured with sliding calipers or osteometric board [27].
  • IIMT - Greater sciatic notch height: distance from the postero-inferior iliac spine (defined as the point of intersection between the auricular surface and the posterior portion of the sciatic notch) to anterior border of the great sciatic notch. Axis of the measurement must be perpendicular to the anterior border. Due to the configuration of hip bone, it is easier to use small arms of the sliding caliper [27].
  • ISMM - Ischium post-acetabular length: distance from the most anterior and inferior point of the ischial tuberosity to the furthest point on the acetabular border [29].
  • SCOX - Iliac or coxal breadth: distance between the anterior-superior iliac spine and the postero-superior iliac spine [27].
  • SS - Spino-sciatic length: minimum distance between the antero-inferior iliac spine and the deepest point in the greater sciatic notch [28].
  • SA - Spino-auricular length: distance between the antero-inferior iliac spine and the auricular point. Auricular point is defined as the intersection of the arcuate line with the auricular surface [28].
  • SIS - Cotylo-sciatic breadth: distance between the lateral border of the acetabulum and the midpoint of the anterior portion of the great sciatic notch. Fixed arm of the sliding caliper is parallel to the acetabular plane [27].
  • VEAC - Vertical acetabular diameter: maximum vertical diameter of the acetabulum, measured on the acetabular rim, as a prolongation of the longitudinal axis of the ischium [27].
The ten variables are displayed in decreasing order of discriminant interest. The authors of these pivotal studies [10, 11] recommend the first eight variables for sex estimation. The last two dimensions (SIS and VEAC) should mainly be reserved for incomplete bones. All the variables were measured with a standard non-digital sliding caliper and a spreading caliper as proposed by Murail and colleagues [10].
Following the creation of this spreadsheet in 2005, owing to its lack of feasibility, a new scoring software called DSP2 was created in 2017 [11]. Consequently, the analysis within the current study was performed using the DSP2 updated software (http://projets.pacea.u-bordeaux.fr/logiciel/DSP2/dsp2.html), which utilizes Fisher’s linear discriminant analysis (LDA). More detailed information about this mathematical approach is described thoroughly in the original studies [10, 11].

Statistical analyses

The sex estimation methodology was applied to 157 available mature individuals at that time, using with whom intra-rater reliability, asymmetry and applicability analyses were performed (refer to aims of the study).
In order to address the objectives of this present research, three consecutive sets of measurements were taken in a row from the same individuals: the first set from the left innominate (S1), the second set from the right innominate (S2), and the third set from the left innominate again (S3).
The first and the third sets of measurements (S1 vs. S3) were compared to analyze the intra-observer reliability (n = 157). To do this, a two-way random intraclass correlation coefficient (ICC) was computed, due to the nature and characteristics of the data. Due to the data characteristics, absolute agreement ICC type was used and, as reported by Daniel [30], single measures should be employed when intra-observer performance was tested. Obtained ICC values were interpreted according to Koo and Li [31], wherein ICC values lower than 0.5 are indicative of poor reliability, values between 0.5 and 0.75 indicate moderate reliability, values between 0.75 and 0.9 indicate good reliability and values higher than 0.90 indicate excellent reliability. The second and the third sets (S2 vs. S3) were compared to establish potential directional asymmetries (n = 157) within the os coxae. For this specific analysis, paired t-test and Wilcoxon test was used for normal and non-normal variables, respectively, as and where applicable.
Regarding sexual differences within the DSP2 variables (n = 140), student T-test or Mann-Whitney analysis was performed depending on whether the variable follows a normal or a non-normal distribution, respectively.
To estimate accuracy for sexing, S2 (right side) and S3 (left side) were analyzed. Two parameters were computed following the original publication [11]:
a)
Percentage of sexing (% sexing), which constitutes the percentage of specimens whose sex was estimated. To establish the percentage of sexing, a posterior probability equal or superior to 0.95 was considered to be the sex classification threshold.
 
b)
Percentage of accuracy (% accuracy), which is the percentage of specimens whose sex has been correctly estimated among those calculated.
 
The % sexing parameter is different to % applicability as the former considers the percentage of specimens that were classified as male or female (with a posterior probability ≥ 0.95, leaving the undetermined ones out), and the latter takes into account the percentage of specimens where specific variables could be measured based on the individual preservation.
All tests were undertaken using SPSS 29.0. For all statistical assessments, a p-value lower than 0.05 was considered statistically significant.

Results

Based on the values mentioned in the Methods Sect. [31], excellent reliability was achieved during intra-observer analysis for 8 out of 10 DSP variables, with good reliability for PUM and moderate reliability for IIMT (Table 2). Scatterplots of S1 vs. S3 for the variables PUM and IIMT have been displayed as Supporting Information (Supplementary Images 1 and 2) to provide a visual complement to the obtained reliability results.
Table 2
Intraclass correlation coefficient (ICC) for intra-observer error analysis for the 10 variables of DSP methodology (N = 157) (results obtained on comparing the sets 1 and 3 (S1 vs. S3))
Variable
ICC
95% IC
p - value
PUM
0.885
0.806–0.928
< 0.001
SPU
0.949
0.928–0.964
< 0.001
DCOX
0.970
0.953–0.980
< 0.001
IIMT
0.659
0.167–0.838
< 0.001
ISMM
0.969
0.956–0.978
< 0.001
SCOX
0.942
0.969–0.984
< 0.001
SS
0.975
0.962–0.983
< 0.001
SA
0.929
0.902–0.949
< 0.001
SIS
0.972
0.960–0.980
< 0.001
VEAC
0.953
0.935–0.966
< 0.001
PUM: Acetabulo-symphyseal pubic length; SPU: Cotylo- pubic width; DCOX: Innominate or coxal length; IIMT: Greater sciatic notch height; ISMM: Ischium post-acetabular length; SCOX: Iliac or coxal breadth; SS: Spino-sciatic length¸SA: Spino-auricular length; SIS: Cotylo-sciatic breadth; VEAC: Vertical acetabular diameter. Significant results are marked in bold
Regarding potential directional asymmetries, results are displayed in Table 3. Significant differences were observed between the two sides in four variables (DCOX, IIMT, ISMM and SA), while no significant differences between left and right os coxae were achieved with the rest of the DSP variables. In the case of DCOX, IIMT and SA, measurements for the left os coxa were significantly higher than right ones, while the opposite was observed for ISMM.
Table 3
Directional asymmetry analyses of the DSP2 variables (comparing sets 2 and 3 (S2 vs. S3)) (N = 157)
Variable
S2 (right)
S3 (left)
T-test
Fd
Wilcoxon Z
p - value
PUM
70.59
70.66
x
x
-0.423
0.672
SPU
26.29
26.31
x
x
-0.387
0.699
DCOX
202.28
202.89
x
x
-2.151
0.031
IIMT
43.06
43.83
-2.264
123
x
0.013
ISMM
106.39
105.42
x
X
-4.764
< 0.001
SCOX
154.32
154.49
-0.607
110
x
0.273
SS
69.82
70.00
-0.940
140
x
0.174
SA
74.77
75.80
x
X
-3.011
0.003
SIS
37.39
37.38
0.043
143
x
0.483
VEAC
54.57
54.72
x
x
-0.884
0.377
PUM: Acetabulo-symphyseal pubic length; SPU: Cotylo- pubic width; DCOX: Innominate or coxal length; IIMT: Greater sciatic notch height; ISMM: Ischium post-acetabular length; SCOX: Iliac or coxal breadth; SS: Spino-sciatic length¸SA: Spino-auricular length; SIS: Cotylo-sciatic breadth; VEAC: Vertical acetabular diameter. Significant results are marked in bold
A comparison of minimum and maximum values for each of the ten DSP variables obtained in the present study, against those reported by Bruzek et al. [11], indicated that all values are within the range reported in the original study [11] (Supplementary Table 1). The only current value that is not falling within the range variation shared by the original authors in the software platform was VEAC, which exceeded the provided maximum score (69 mm vs. 66.5 mm). Nevertheless, it is important to maintain caution during such a comparison, as the original study did not mention the side associated with these measurements, and to maintain uniformity, comparison measurements within the present study have been obtained by combining the right (S2) and left (S3) values.
Regarding sexual dimorphism of the DSP variables for the right and left sides, descriptive statistics are displayed in Table 4. Overall, higher mean values were found in males compared to females except for PUM and IIMT, where the opposite pattern was observed. On the right side (S2), all the DSP variables were significantly sexually dimorphic barring PUM, while on the left side (S3), neither PUM nor SA mean values were significantly different between males and females. The rest of the variables exhibited significant sexual dimorphism.
Table 4
Descriptive statistics (by sex) for the os coxae variables in the documented sample (N = 140)
Variable
N (F)
Mean (F)
SD
(F)
Min (F)
Max (F)
N (M)
Mean (M)
SD
(M)
Min (M)
Max (M)
p -value
(t-test)
p – value
(Mann-Whitney U)
PUM (R)
56
71.20
4.775
62
85
63
70.26
3.471
61
78
 
0.514
SPU (R)
56
23.03
2.339
19
31
63
28.89
2.813
21.4
35
< 0.001
 
DCOX (R)
55
190.49
8.117
172
210
66
212.03
11.093
175
236
 
< 0.001
IIMT (R)
57
44.71
4.810
33
57.6
58
41.52
4.416
32.6
51
< 0.001
 
ISMM (R)
57
99.12
4.722
90
113.6
65
112.52
5.730
96.6
125
 
< 0.001
SCOX (R)
49
149.98
6.969
133
168
57
157.79
8.546
136
174
< 0.001
 
SS (R)
62
65.45
3.754
58
76.4
70
73.45
4.482
62
83
 
< 0.001
SA (R)
62
73.26
5.750
57.6
89.7
68
75.43
5.992
61
90
0.019
 
SIS (R)
62
35.03
3.295
28
41
71
39.52
3.333
31
46
< 0.001
 
VEAC (R)
60
51.53
3.008
44
62
70
57.36
3.902
49
69
 
< 0.001
PUM (L)
57
71.07
4.651
61
84
63
70.34
4.151
59
81.6
0.182
 
SPU (L)
61
22.84
2.333
19
29.3
67
28.92
2.582
21
37
 
< 0.001
DCOX (L)
60
192.10
9.311
172
216
65
212.45
11.054
176
238
 
< 0.001
IIMT (L)
57
45.60
4.560
36
58.6
63
42.49
4.028
31
51
< 0.001
 
ISMM (L)
61
98.52
5.113
87.6
112
66
111.35
5.810
95
124
 
< 0.001
SCOX (L)
52
150.85
7.188
133
167
60
157.82
8.825
136
181
< 0.001
 
SS (L)
64
65.81
3.633
57.7
73.7
69
73.36
4.593
64
85
 
< 0.001
SA (L)
64
74.95
6.106
62
92
69
76.54
5.771
65.6
92
0.063
 
SIS (L)
65
35.11
3.289
28
42
71
39.32
3.287
31.6
46.4
< 0.001
 
VEAC (L)
65
51.45
2.657
45
58
71
57.79
3.944
48.8
67
 
< 0.001
PUM: Acetabulo-symphyseal pubic length; SPU: Cotylo- pubic width; DCOX: Innominate or coxal length; IIMT: Greater sciatic notch height; ISMM: Ischium post-acetabular length; SCOX: Iliac or coxal breadth; SS: Spino-sciatic length¸SA: Spino-auricular length; SIS: Cotylo-sciatic breadth; VEAC: Vertical acetabular diameter. (F): female subsample; (M): male subsample; (R): right innominate (set 2); (L): left innominate (set 3). Significant results are marked in bold
According to sample preservation, % applicability for every single DSP variable in a sex-pooled sample was higher than 85% in all cases, except for the variable SCOX, where the values were around 80% on both sides (Table 5). Similar results were achieved in males and females separately, with the exception of the right male subsample for IIMT, where the percentage was 81.69%. In the combined sample, larger applicability values were achieved on the left side in all cases, with the exceptions of PUM, SS and SIS. In the sex-specific samples, some variables achieved right predominance and others demonstrated a left predominance, with no consistent pattern. Besides, some of these side differences coincided in males and females separately (PUM, SPU, ISMM, SCOX, SS, VEAC), whereas others did not (DCOX, IIMT, SA, SIS). Regarding applicability for sexing between the two sexes, higher percentages were found in females for most of the DSP variables in the right subsample, except for DCOX, SCOX and VEAC. In the case of SIS, both sexes achieved 100%. On the left sample, however, all female features achieved better results than male ones, with the exception of SCOX.
Table 5
Percentage of applicability of the individual variables of DSP2 on the studied sample
 
Males (%)
Females (%)
Total (%)
Right
Left
Right
Left
Right
Left
PUM
88.73
87.50
90.32
87.69
89.33
88.24
SPU
88.73
93.06
90.32
93.85
88.67
93.46
DCOX
92.96
90.28
88.71
92.31
90.00
90.85
IIMT
81.69
87.50
91.94
87.69
86.67
88.24
ISMM
91.55
91.67
91.94
93.85
92.00
92.16
SCOX
80.28
83.33
79.03
80.00
79.33
81.70
SS
98.59
95.83
100.00
98.46
98.00
97.74
SA
95.77
95.83
100.00
98.46
96.67
97.39
SIS
100.00
98.61
100.00
100.00
100.00
97.39
VEAC
98.59
98.61
96.77
100.00
98.00
98.69
PUM: Acetabulo-symphyseal pubic length; SPU: Cotylo- pubic width; DCOX: Innominate or coxal length; IIMT: Greater sciatic notch height; ISMM: Ischium post-acetabular length; SCOX: Iliac or coxal breadth; SS: Spino-sciatic length¸SA: Spino-auricular length; SIS: Cotylo-sciatic breadth; VEAC: Vertical acetabular diameter. Global dataset (n = 157) was used for these calculations in the pooled sample while the documented sample (n = 140) was used to perform the sex-specific calculations. Applicability refers to the number of individuals out of the total where the specific variable could be measured due to preservation
Concerning the accuracy of right (S2) and left (S3) datasets, general outcomes showed that accuracy percentages were high, being > 94% regardless of the number of variables used (Table 6). Similar values (around 97%) were reached with all variables, the first 8, or the most accurate 4 variables. In fact, even with the worst 4 variables, the accuracy % reached 94.74% and 94.55% for left and right datasets, respectively. Thus, it appears that having the measurements of the first 4 variables is enough to obtain the highest accuracy possible within this pooled sample. However, for the percentage of sexing, the results were different: while similar values were achieved with 10 or the first 8 variables, the values slightly decreased with the best 4 variables and reduced to half with the worst 4 variables. These results were similar when sexes were analyzed separately (Table 6). Thus, accuracy values were always higher than 90% in males and higher than 95% in females, meanwhile sexing percentages decreased when the number and quality of variables decreased as well. However, if the sexes are compared, the females’ results are always higher than the males’ ones, both for sexing and accuracy percentages. The singular exception to this observation is the sexing percentage with the four worst variables on both sides, where the number of estimated males is superior to the estimated females. Lastly, considering sides in the pooled sample, the left dataset achieved better accuracy results in all cases. The same occurred in most of the cases regarding sexing percentages. When sexes are considered in isolation, no clear side pattern was identified, as better results were achieved for left and right datasets in different variable-based categories.
Table 6
Sexing accuracy results with various combinations of variables within the documented sample (N = 140)
 
Undetermined / N
(% sexing) (F)
Number of errors / determined N
(% accuracy) (F)
Undetermined / N
(% sexing) (M)
Number of errors / determined N
(% accuracy) (M)
Undetermined / N
(% sexing)
(Total)
Number of errors / determined N
(% accuracy)
(Total)
All available variables (L)
1 / 65
(98.46)
0 / 64
(100)
11 / 72
(84.72)
2 / 61
(96.72)
12 / 137
(91.24)
2 / 125
(98.40)
All available variables (R)
3 / 62
(95.16)
0 / 59
(100)
9 / 71
(87.32)
3 / 62
(95.16)
12 / 133
(90.98)
3 / 121
(97.52)
10 variables (L)
0 / 45
(100)
0 / 45
(100)
6 / 48
(87.50)
1 / 42
(97.62)
6 / 93
(93.55)
1 / 87
(98.85)
10 variables (R)
0 / 44
(100)
0 / 44
(100)
5 / 46
(89.13)
2 / 41
(95.12)
5 / 90
(94.44)
2 / 85
(97.65)
First 8 variables (L)
0 / 45
(100)
0 / 45
(100)
6 / 49
(87.76)
1 / 43
(97.67)
6 / 94
(93.62)
1 / 88
(98.86)
First 8 variables (R)
0 / 44
(100)
0 / 44
(100)
5 / 46
(89.13)
2 / 41
(95.12)
5 / 90
(94.44)
2 / 85
(97.65)
Best 4 variables (L)
2 / 47
(95.83)
0 / 45
(100)
9 / 55
(83.64)
2 / 46
(95.65)
11 / 103
(89.32)
2 / 92
(97.83)
Best 4 variables (R)
0 / 47
(100)
0 / 47
(100)
12 / 51
(76.47)
2 / 39
(94.87)
12 / 98
(87.76)
2 / 86
(97.67)
Worst 4 variables (L)
40 / 64
(37.50
0 / 24
(100)
34 / 67
(49.25)
3 / 33
(90.91)
74 / 131
(45.51)
3 / 57
(94.74)
Worst 4 variables (R)
40 / 60
(33.33)
1 / 20
(95.00)
32 / 67
(52.24)
2 / 35
(94.29)
72 / 127
(43.31)
3 / 55
(94.55)
% sexing means the percentage of specimens whose sex has been determined (p ≥ 0.95) while % accuracy means the percentage of specimens whose sex has been correctly determined among those determined. Results are given for both sides separately and, regarding biological sex, for the pooled sample and each sex separately. First 8 variables: without SIS and VEAC. Best 4 variables: DCOX, PUM, SPU and IIMT. Worst 4 variables: SIS, VEAC, SA and SS. (L): left. (R): right. (F): female. (M): male
With the aim of investigating the relevance of the posterior probability threshold for accuracy estimations, previous outcomes were compared against sexing accuracy obtained by decreasing the posterior probability from 95% (as original authors advised) to 85% (Table 7). The percentage of sexing increased in all cases, with a significant increase observed in males. Nevertheless, decreasing the posterior probability by 10% also reduced the percentage of accuracy in most cases, with few right-side exceptions where similar results were obtained.
Table 7
Results with various combinations of variables based on the posterior probability (95% vs. 85%) within the documented sample (N = 140)
 
Posterior probability ≥ 0.95
Posterior probability ≥ 0.85
Results
N (total)
% sexing
% accuracy
% sexing
% accuracy
Sexing
(M)
Sexing
(F)
Number of new errors
(M)
Number of new errors
(F)
All available variables (L)
91.24
98.40
94.90
97.69
+ 5 (11)
+ 0 (1)
+ 1 (5)
+ 0 (0)
137
All available variables (R)
90.98
97.52
96.24
97.66
+ 7 (9)
+ 0 (3)
+ 0 (7)
+ 0 (0)
133
10 variables (L)
93.55
98.85
97.85
97.80
+ 4 (6)
+ 0 (0)
+ 1 (4)
+ 0 (0)
93
10 variables (R)
94.44
97.65
97.78
97.73
+ 3 (5)
+ 0 (0)
+ 0 (3)
+ 0 (0)
90
First 8 variables (L)
93.62
98.86
97.87
97.83
+ 4 (6)
+ 0 (0)
+ 1 (4)
+ 0 (0)
94
First 8 variables (R)
94.44
97.65
97.78
97.73
+ 3 (5)
+ 0 (0)
+ 0 (3)
+ 0 (0)
90
Best 4 variables (L)
89.32
97.83
95.15
96.94
+ 4 (9)
+ 2 (2)
+ 1 (4)
+ 0 (2)
103
Best 4 variables (R)
87.76
97.67
96.94
96.84
+ 9 (12)
+ 0 (0)
+ 1 (9)
+ 0 (0)
98
Worst 4 variables (L)
45.51
94.74
76.34
93.00
+ 17 (34)
+ 26 (40)
+ 3 (17)
+ 1 (26)
131
Worst 4 variables (R)
43.31
94.55
66.14
92.86
+ 19 (40)
+ 10 (32)
+ 3 (19)
+ 0 (10)
127
% sexing means the percentage of specimens whose sex has been determined (p ≥ 0.95) while % accuracy means the percentage of specimens whose sex has been correctly determined among those determined. Results are given for both sides separately and, regarding biological sex, for the pooled sample and each sex separately. First 8 variables: without SIS and VEAC. Best 4 variables: DCOX, PUM, SPU and IIMT. Worst 4 variables: SIS, VEAC, SA and SS. L: left. R: right. F: female. M: male
In the “Sexing” columns belonging to “Results”: 1) Plain numbers means the number of individuals who were determined with the 0.85 threshold but not with the 0.95 one. The number between parentheses shows the total number of undetermined individuals with the 0.95 threshold. In the “Number of new errors” columns belonging to “Results”: 1) Plain numbers means the number of new committed errors in sex estimation when using the 0.85 threshold instead of the 0.95 one. The number between parentheses shows the number of individuals who were determined with the 0.85 threshold but not with the 0.95 one

Discussion

Sex estimation is one of the first procedures towards human identification within medicolegal and forensic contexts. Accurate sex estimation can also contribute to providing important insights into population history and migration patterns. Therefore, this step is an essential tool for forensic anthropologists and archaeologists, and it is crucial for a comprehensive understanding of human evolution, biology, and health. Numerous research has previously been published on metric sex estimation for diverse Spanish samples, using different skeletal elements: the skull [32], the dentition [33, 34], the clavicle [3537], the sternum [38], the ribs [39, 40], the vertebrae [4143], the sacrum [44], the radius [45], the carpals [46], the femur [47, 48], the patella [37, 49], the tibia [50, 51], the talus [45], the navicular [52] or the metacarpals [53]. However, despite its direct association with parturition and proven accuracy for being the most dimorphic human bone, specific research on sex estimation using hipbone measurements is currently limited for this biogeographical population [47, 54]. In this respect, to the best of our knowledge, DSP2 has not been tested in any Spanish sample, so comparisons along this line are not feasible.

Reliability

Overall, the current study shows excellent results for intra-rater reliability analysis, coinciding with previous literature for pelvic measurements [15, 55, 56]. However, good and moderate results were achieved with PUM and IIMT, respectively, yielding lower ICC values compared to the ones reported by de Almeida in a Brazilian sample [15]. The comparatively lower values for sciatic greater notch (IIMT) have already been reported during previous reliability analyses [15, 55], and with CT-based studies [19, 20]. These results are likely due to different factors such as the greater difficulty associated with identifying the anatomical landmarks and placing the sliding caliper in the correct position, which requires the user to visually check a right angle between the postero-inferior iliac spine and the anterior border of the greater sciatic notch [27]. In addition, it is worth highlighting that these outcomes contrast with the fact that both features, PUM and IIMT, belong to the first four DSP variables, considered to have the highest discrimination power [10]. Consequently, special care should be taken when using these specific variables, and better descriptions and/or images could be provided in future DSP updates.

Applicability

The current percentage applicability for SCOX was lower in comparison to other variables. This outcome corroborated previous literature results [11, 13, 14]. However, those authors reported similar lower values for PUM, contrasting to our findings. Furthermore, overall better female preservation (% applicability: possibility of taking the measurements) compared to males was found (except SCOX), contrasting to the higher gracility and associated fragility of skeleton of women. This could be linked to their belonging to a documented collection from modern cemeteries, with different taphonomic processes or artificial barriers such as coffin protection, slowing down the natural human decomposition. In addition, the female mean age was significantly higher than the male’s in this study sample, rendering their skeletons more prone to be vulnerable and fragmentary, so the current results regarding applicability should be explained by other different factors. The SCOX exception, on the other hand, may be due to both postero-superior and antero-superior spines involved in the measurement. These landmarks are likely to be more robust, and so preservable in males due to anatomical muscular attachments.

Sexing and accuracy percentages

Overall results

Current results show that, whereas the sexing % decreased progressively when the number of variables or their discrimination power was reduced, the accuracy % remained high irrespective of the combination of employed variables. A comprehensive comparison to previously reported similar literature is shown in Table 8. Overall, results from all ten, or the first eight variables are almost identical across the table, so it appears that when the first eight variables are available for analysis, incorporating the remaining two (SIS and VEAC) does not render better outcomes. As advocated by Murail et al. and Bruzek et al. [10, 11], the last two features are useful within degraded and/or fragmentary contexts, where other more accurate variables are non-viable. In such scenarios, these variables with relatively lower accuracy can aid in identification by helping achieve the minimum four-variable requirement mandated by the DSP software.
Table 8
Comparison of results across literature and the present study when applying DSP methodology in pooled samples belonging to diverse populations based on the number of variables used
TOTAL
10 variables
8 variables
“Best” 4 variables
“Worst” 4 variables
Reference
Geographical origin
N
% sexing
% accuracy
% sexing
% accuracy
% sexing
% accuracy
% sexing
% accuracy
Murail et al., 2005 [10]
European (UK, France, Portugal)
454
-
-
95.9
100
92.8
100
69.7
98.3
Murail et al., 2005 [10]
African American 1
329
-
-
92
98.6
86.9
98.6
66.1
98.6
Murail et al., 2005 [10]
European American 1
311
-
-
93
100
89.5
99.6
65
97.4
Murail et al., 2005 [10]
European + North American
1094
-
-
99.7
99.3
86.9
99.7
76
99.6
Murail et al., 2005 [10]
Thailand 2
198
-
-
94.1
100
90.5
100
75.5
100
Murail et al., 2005 [10]
Lithuania 2
220
-
-
94.4
100
91.7
100
71.6
98.7
Murail et al., 2005 [10]
South Africa – Zulu 2
306
-
-
88.7
98.8
84.6
98.8
66.2
99
Murail et al., 2005 [10]
South Africa – Soto 2
110
-
-
86
100
84.4
100
63
100
Murail et al., 2005 [10]
South Africa – Afrikaner 2
112
-
-
95.1
100
88.8
100
70.8
100
Murail et al., 2005 [10]
Worldwide
2040
90.71
99.63
90.76
99.63
86.69
99.61
40.23
98.75
Sánchez-Mejorada et al., 2011 [14]
Mexico
250
89.2
100
-
-
-
-
-
-
Chapman et al., 2014 [18]
Belgium
39
97.4
100
97.44
100
89.74
100
53.85
90.48
Bruzek et al., 2017 [11]
France
160
89.93
100
90.07
100
83.22
99.19
45.57
100
Bruzek et al., 2017 [11]
Portugal
232
89.64
100
89.69
100
86.54
98.33
44.78
99.03
Bruzek et al., 2017 [11]
United Kingdom
62
86.54
100
86.54
100
80.7
100
32.79
100
Bruzek et al., 2017 [11]
Lithuania
220
95.39
100
95.41
100
92.73
100
39.91
100
Bruzek et al., 2017 [11]
South Africa - Zulu
306
88.44
99.23
88.78
99.23
84.85
100
33.44
98.04
Bruzek et al., 2017 [11]
South Africa - Soto
110
85.44
100
85.44
100
80.73
100
43.4
95.65
Bruzek et al., 2017 [11]
South Africa - Afrikaner
112
93.62
100
94
100
89.72
100
43.27
100
Bruzek et al., 2017 [11]
European American
112
93.62
100
93.68
100
90.48
100
42.45
100
Bruzek et al., 2017 [11]
African American
113
90.2
98.91
90.2
98.91
87.04
100
40.18
97.78
Bruzek et al., 2017 [11]
European American
199
88.24
100
89.01
100
84.02
99.39
49.22
97.89
Bruzek et al., 2017 [11]
African American
216
91.71
98.4
91.39
98.43
89.57
98.41
45.02
96.84
Bruzek et al., 2017 [11]
Thailand
198
94.62
100
94.62
100
91.1
100
38.14
100
Bruzek et al., 2017 [11]
North America
120
93.46
99
93.58
99.02
87.27
98.96
50.86
94.92
Bruzek et al., 2017 [11]
Switzerland
503
94.74
96.03
94.78
96.06
90.91
96.88
55.25
98.06
Bruzek et al., 2017 [11]
Worldwide
2040
90.84
99.65
90.98
99.65
87.17
99.53
41.49
98.67
Quatrehomme et al., 2017 [12]
France
100
94.83
100
94.92
100
76.92
100
52.87
100
Salles Machado et al., 2018 [17]
Brazil
103
85.43
88.34
-
-
82.52
90.29
60.19
93.20
Rodriguez Paz et al., 2019 [20]
Denmark
116
93.9
100
93.1
100
81.9
100
49.7
98.2
Kranioti et al., 2019 [13]
Greece
133
88.00
97.43
-
-
-
-
-
-
De Almeida et al., 2020 [15]
Brazil
301
94.00
99.3
94.7
99.3
90.7
100
61.0
98.9
Rodrigo de Oliveira Lopes et al., 2023 [16]
Brazil
128
-
-
-
-
71.09
92.97
-
-
Oh et al., 2023 [24]
South Korea
29
86.2
86.2
89.66
86.2
85.00
80
31.3
31.03
Current study (right)
Spain
140
94.44
97.65
94.44
97.65
87.76
97.67
43.31
94.55
Current study (left)
Spain
140
93.55
98.85
93.62
98.86
89.32
97.83
45.51
94.74
1Results reported from Murail et al. testing the European model (reference) on North American target samples
2Results reported from Murail et al. testing the European and North American model (reference) on different targets: Asian (Thailand), African (South Africa) and European (Lithuania) samples
% sexing means the percentage of specimens whose sex has been determined (p ≥ 0.95) while % accuracy means the percentage of specimens whose sex has been correctly determined among those determined
Sexing % values obtained with all ten variables in the present study were 94.44% and 93.55% for the right and left halves, respectively, which is slightly lower than the 97.40% reported by Chapman et al. [18], the maximum value found in the literature, and higher than the 85.43% reported by Salles Machado et al. [17], the minimum value achieved across referenced studies (Table 8). Regarding % accuracy, the present study achieved 97.65 and 98.85 (right and left, respectively), within the range from the minimum 86.20% [24] to the maximum, 100.0% [11, 12, 14, 1820]. A comparative analysis (Table 8) indicates that general % accuracy results are consistently high in literature, with most of the authors reporting values higher than 95% with only two exceptions: a Brazilian miscegenated population [17] and a very small sample from South Korea [24]. In fact, several authors found no cases of misclassification during their sex estimation by DSP [11, 12, 14, 1820]. In the current study, this sort of success rate was achieved only in females.
The present results of % accuracy with the best 4 variables were 97.67% and 97.83% for right and left, respectively. According to the previous studies (Table 8), the reported results ranged from 80% [24] to 100% [1012, 15, 18, 20]. However, the lowest value (80%) came from an already mentioned small sample from Korea comprising of only 29 individuals. The second lowest result generated with a larger sample size (n = 103) was reported as 90.29% [17]. In this specific case [17], the results for % accuracy should be taken with caution since some reported values are unexpected and difficult to justify; i.e. they rendered 88.34%, 90.29% and 93.20% using 10 variables, best 4 variables and worst 4 variables, respectively. Continuing with best 4 variables results, all other studies yielded accuracy percentages higher than 90%. However, outcomes of % sexing are quite different: while the present study’s ones were 87.76% and 89.32% for right and left sides, respectively, previously literature results ranged from 71.09% [16] to 92.8% for a specific European subsample [10].
Results of the worst 4 variables achieved good accuracy % outcomes in the present study: 94.55% and 94.74% for the right and left sides, respectively. Regarding previous studies, if the Korean small sample study is not considered due to its smaller sample size, the results ranged between 90.48% [18] and 100% [1012]. In the case of the % sexing, the scenario is different. The minimum outcome was reported in a British subsample published by the original authors [11] as 32.79%, while the maximum was also found within the original publication [10] as 76%. Murail and colleagues’ original publication reported a sexing % of 40.23% in the worldwide sample (n = 2040) but, surprisingly, higher outcomes were reported in its different subsamples (even when 7 out of 9 of them were testing reference models on geographically different target samples), ranging from 63 to 76%. The rest of the revised literature, including the updating of DSP as DSP2 [11], reported % sexing between 32.79% [11] and 61.0% [15]. A scientific explanation for Murail’s differential findings is currently lacking.
One of the drawbacks of DSP compared with other discriminant analysis is the high number of undetermined cases that the software generates, especially when a reduced number of variables are considered. These results arise of the original authors decision about employing a 0.95 threshold instead of the 0.50 value. This settlement, however, guarantees very high levels of accuracy, with 100% or close values with a combination of the most discriminant variables. Interestingly, even taking into account just the four variables with relatively lower discrimination power (SS, SA, SIS and VEAC), accuracy percentages were lower than 94.0% in just 3 out of 32 revised literature outcomes, including the Korean one with a sample size of 29 individuals. Nevertheless, as other authors have suggested [20], the poorer results with the worst 4 combination of variables (or with a reduced number of variables) need to be interpreted with caution and complemented with non-metric methodologies.
In the present study, the posterior probability threshold was decreased from 95 to 85% to assess its potential impact on % sexing and % accuracy. This resulted in an increase in the % sexing in all cases in exchange of reduced % accuracy in most of the cases. Since the current female outcomes were comparably better than males, most of the changes were associated with sexing in males: improvement by increasing the sexing rate but gaining imprecision by incorporating errors. While this reduced accuracy still has acceptable values, the reduction in posterior probability is not recommended within future forensic practice from a reliability point of view, as a decrease in the number of indeterminate bones does not necessarily make up for decreased reliability and accuracy. Given the medico-legal and forensic contexts of interest here, an unreliable sex estimation approach can be more problematic than an unapplicable one [57, 58]. Furthermore, the reduction in posterior probability here, by and large, also resulted in a decrease in % accuracy, negating the need for this reduction. Moreover, even with a 95% posterior probability, % accuracy obtained in the present study is high (even with the worst four variables), demonstrating an excellent applicability for the DSP2 approach when it comes to sex estimation.
In relation to misclassification cases, some documentary or human error should not be completely ruled out in the osteological collection itself, since worldwide researchers and curators work with them all the time and misplacing skeletal elements or typographical errors could be contributing factors [18, 59].

Side differences

Most of the authors who have analyzed DSP performance in diverse populations have used the left side throughout to be consistent [13, 15, 17, 18, 20]. However, some researchers used left and right hip bones in their studies, combining both sides without analyzing for potential differences [14, 19]. Whereas other studies only partially examined them [12, 16]. The present study has found higher values in all left cases compared to the right-side results, apart from ISMM, with opposite results, and a quite identical mean value in SIS between sides. However, these differences were only statistically significant in DCOX, IIMT, ISMM and SA. This finding could not be corroborated as no similar results have been reported previously, warranting further investigation into the causality of this anomaly. In fact, other authors concluded that the DSP values from the right and left coxal bones were comparable [12], even suggesting that single measurements may be substituted in cases of non availability of both halves of the pelvis. This absence of asymmetry agrees with previous results from a CT-based investigation which utilised different pelvic measurements [60].
Overall, current results did not indicate any clear side-based results regarding the % sexing in different number of variables sets. However, left side achieved better % accuracy compared to the right in all cases (Table 6). In females, similar results were found. No differences were displayed in most of the cases of % accuracy in females as left and right sides both achieved 100%. In males, on the other hand, right side displayed higher % sexing in all cases except for the best 4 variables, while left side achieved better % accuracy than right side with one exception: the worst 4 variables case. The only previous investigation to compare those results was from Rodrigo de Oliveira Lopes et al. [16], who reported accuracy comparison for the best 4 variables (PUM, SPU, DCOX, IIMT). These authors found higher % sexing and % accuracy in the left side in females and in the right side in males, i.e., contrasting findings in comparison to the present study (Table 6). Accuracy % results in females were not comparable because both left and right sides achieved 100% in the present study.

Sexual differences

Neither PUM nor SA mean metric values were found to have significant differences between sexes in the left side coinciding with Salles Machado et al. [17]. In the right side, PUM alone did not exhibit significant sex differences, a result unreported in the literature. Other authors describe non-significant differences between males and females in SA [11, 1315, 19] and in the combination of PUM, SCOX and SA [12]. These PUM results highly contrast with the fact that this variable has the highest discrimination power across the analyzed ten variables according to the DSP creators [10], data which contrasts with Kranioti et al., who described the four most discriminant variables as ISMM, SPU, DCOX and VEAC in a Greek sample [13].
Tables 9 and 10 display the comparison of sex-specific percentages of sexing and accuracy depending on the number of DSP variables used across scientific literature. In the female comparative analysis (Table 9), the present study achieved 100% in most of the cases of % sexing in the first three sets (10, 8 and best 4 variables), exceeding the reported outcomes in other samples. Regarding % accuracy, no misclassification cases were reported here, agreeing with the ones rendered in Mexican [14], French [12, 19] and Brazilian [15] samples. However, the low % sexing exhibited in French (41.66%) compared to the rest of analyzed samples using the best four variables, ranging from 85.2 to 100%, is hard to explain, and is more similar to results from the set of the worst 4 variables. Since some of the values reported by Quatrehomme et al. [12] are internally inconsistent within their own tables, these results could have been caused by formatting typos and should be compared with caution. In the case of the worst 4 variables, present results are slightly lower than other studies [11, 12, 17]. It is remarkable that the high percentage achieved in this case by de Almeida and colleagues [15] in a Brazilian sample (81.2%), is more similar to the results of 10, 8 or best 4 variables in other geographical regions.
Table 9
Comparison of literature results with current ones when applying DSP methodology in female samples belonging to diverse populations based on the number of variables used
FEMALES
10 variables
8 variables
“Best” 4 variables
“Worst” 4 variables
Reference
Geographical origin
N
% sexing
% accuracy
% sexing
% accuracy
% sexing
% accuracy
% sexing
% accuracy
Sánchez-Mejorada et al., 2011 [14]
Mexico
118
98.31
100
-
-
-
-
-
-
Mestekova et al., 2015 [19]
France
54
97.2
100
-
-
85.2
100
-
-
Bruzek et al., 2017 [11]
Worldwide
1023
90.96
99.29
91.21
99.30
87.55
99.53
42.54
98.82
Quatrehomme et al., 2017 [12]
France
-
85.71
100
94.91
100
41.66
100
40.48
100
Salles Machado et al., 2018 [17]
Brazil
50
98.05
86.00
-
-
92.00
88.00
38.00
82.00
Rodriguez Paz et al., 2019 [20]
Denmark
67
97.0
-
-
-
93.3
-
-
-
De Almeida et al., 2020 [15]
Brazil
136
94.4
100
95.8
100
88.7
100
81.2
99.0
Rodrigo de Oliveira Lopes et al., 2023 [16]
Brazil
50
-
-
-
-
82.0
96.0
-
-
Current study (right)
Spain
66
100
100
100
100
100
100
33.33
95.0
Current study (left)
Spain
66
100
100
100
100
95.83
100
37.50
100
% sexing means the percentage of specimens whose sex has been determined (p ≥ 0.95) while % accuracy means the percentage of specimens whose sex has been correctly determined among those determined
Table 10
Comparison of literature results with current ones when applying DSP methodology in male samples belonging to diverse populations based on the number of variables used
MALES
10 variables
8 variables
“Best” 4 variables
“Worst” 4 variables
Reference
Geographical origin
N
% sexing
% accuracy
% sexing
% accuracy
% sexing
% accuracy
% sexing
% accuracy
Sánchez-Mejorada et al., 2011 [14]
Mexico
132
81.06
100
-
-
-
-
-
-
Mestekova et al., 2015 [19]
France
52
92.3
100
-
-
96.2
100
-
-
Bruzek et al., 2017 [11]
Worldwide
1017
90.72
100
90.75
100
86.79
99.53
40.44
98.51
Quatrehomme et al., 2017 [12]
France
-
100
100
100
100
97.56
100
64.44
100
Salles Machado et al., 2018 [17]
Brazil
53
89.32
90.57
-
-
73.58
73.58
79.24
100
Rodriguez Paz et al., 2019 [20]
Denmark
49
89.7
-
-
-
86.3
-
-
-
De Almeida et al., 2020 [15]
Brazil
165
93.7
98.6
93.7
98.6
92.4
100
43.5
98.5
Rodrigo de Oliveira Lopes et al., 2023 [16]
Brazil
78
-
-
-
-
64.10
91.03
-
-
Current study (right)
Spain
74
89.13
95.12
89.13
95.12
76.47
94.87
52.24
94.29
Current study (left)
Spain
74
87.5
97.62
87.76
97.67
83.64
95.65
49.25
90.91
% sexing means the percentage of specimens whose sex has been determined (p ≥ 0.95) while % accuracy means the percentage of specimens whose sex has been correctly determined among those determined
On the other hand, male-specific analysis is showed in Table 10. Regarding the 10-variable and 4-best cases, where more references were reported, current study % sexing are lower than the previous publications, except in Mexican [14] and Brazilian populations [16, 17]. For % accuracy, similar overall lower accuracy was achieved in the current study when compared with other publications with the exception of the Brazilian population [16, 17]. As mentioned previously, Salles Machado et al. [17] results are anomalous and should be considered cautiously; e.g. % accuracy using the worst 4 variables (100%) is higher than the value resulted from using 10 variables (90.57%). With regards to the worst 4 variables results, present % sexing results are higher than Northeastern Brazilian [15] and the worldwide sample utilised by Bruzek and colleagues [11] but lower than the outcomes achieved for France [12] and Southeast Brazil populations [17]. It is worthy to highlight the high percentage achieved by Salles Machado et al. [17] in a Brazilian sample (79.24%), comparable to the results of 10, 8 or best 4 variables in other geographical regions. The existence of an outlier outcome had been found and previously commented in Brazilian females, but in a different sample [15]. These differences could be explained by the great geographical extent and human diversity of this country, likely existing intrapopulation differences between Northeastern [15] and Southeast [17] Brazilian samples. To conclude the comparison, the current % accuracy results for the worst 4 variables in males were lower than all the revised literature ones [11, 12, 15, 17].
Comparing sexes across populations, in the case of the performance of the DSP methodology, both the sexing and accuracy results were better for females than males in most of the cases in the current sample. Higher % sexing, with less undetermined individuals in females, has already been reported in Mexicans [14], Danish [20], Brazilians [16] and the worldwide sample offered by Bruzek et al. [11]. Contrasting results were found for a French population [12]. Furthermore, outcomes in favor of females or males depending on the number of used variables, with no clear sex-specific trend, were found in French [19], Brazilian [15, 17], and Belgians [22]. According to % accuracy, on the other hand, the female predominance compared to males found here agreed with some Brazilian outcomes [15, 16] and were also reported in pre-Columbian mummies [22]. Besides, Bruzek et al. (worldwide sample) found more accurate results in males in the first two subsamples (10 and 8 variables) and coinciding or similar outcomes with the best and worst 4 variables subsamples, respectively [11]. No differences were found in % accuracy between sexes in Mexicans [14], and French [12, 19], where the systematic shared results between sexes were 100%. Contrasting with current findings, Gonzalez et al. examined sexual dimorphism in the great sciatic notch and ischiopubic complex in a Portuguese sample [61], concluding females are misclassified more often than males.

Inter-population differences

Current DSP variables values were within the ranges described by the worldwide sample used by the original authors [10, 11] with the exception of VEAC, where the current data was higher than the worldwide-based maximum threshold reported by Bruzek et al. [11]. Some research [62] stated that skeletal sexually dimorphic characters show inter and intra-population variability and other authors stated that pelvic-based sex determination may be impacted by population differences and sample variability [56, 63]. However, other researchers advocate for the opposite, specifically regarding the pelvis [64]. In keeping with this, Bruzek and colleagues [11] stated that the pelvis shows a similar pattern of sexual dimorphism across diverse geographical areas which appeared approximately 100–150 ky ago in early modern humans, defended by previous literature [6569]. Thus, they offered a worldwide database (software DSP2) of pelvic measurements to any anthropologist who needs to sex skeletal remains, regardless of their geographical origin. This global reference not only comes from samples around the world but also from different ethnical groups (Zulu, Soto, Afrikaner, African American, and European American) and temporal periods (from 18th to late 20th centuries), enhancing their potential applicability in miscellaneous populations. At this respect, it is worthy to stress that when reference models were used to determine the sex of geographically different target populations [10], accuracy results from 97.4 to 100% were displayed (Table 8). However, some large geographical areas were not considered in the reference sample used to calculate the posterior probabilities on DSP2, such as Central or South America. In addition, Africa and Asia were scarcely represented, with just Thai and South African samples analyzed. Although posterior tests on Mexican [14] and Brazilian [15, 16] samples reported comparable percentages of sexing and accuracy, application to miscegenated Brazilian-identified sample [17] yielded lower values compared to published literature (Table 8). Furthermore, similar results arose when DSP2 and population-specific formulae were applied to a Greece sample [13]. However, Kranioti et al. recommended population-specific formulations whenever possible to maximize the outcomes. This existing inter-population variation was also suggested by the application of DSP on Pre-Columbian mummies [22], which garnered lower measurements for the DSP variables when compared to the original reference ranges [11].

Conclusions and future directions

This study investigated thoroughly the application of DSP2 to a Spanish dry skeletal sample. Percentage of sexing was high when 10, first 8 or 4 best variables were considered and reduced to half when the 4 variables with least discrimination power, called worst 4 variables, were utilized. Regarding % accuracy, however, they were high in all cases, especially in females, regardless of the number of variables used. As the original authors described [10], the “worst” combination of four variables only refers to the decreasing percentage of sexed specimens, while the accuracy remains extremely high. The benefits and utility of the DSP method seem to have driven to consolidate also in bioarchaeological contexts [2123, 25, 7072]. However, their actual accuracy on past populations is poorly understood, so further comparison between DSP outcomes on genetic-based documented samples should be implemented in paleontological and archaeological remains.
Despite being restrictive, the suggested posterior probability of 0.95 seems to make the DSP reliable and accurate, rendering it a meaningful tool in forensic practice. Besides, its high flexibility regarding the variables used gives it a special place in forensic anthropology lab routinely working on fragmentary or degraded samples. DSP has also yielded good accuracy results when applied to CT scan images [1820]. These virtual-based results open the possibility to new population-specific tests, which may be performed in geographical areas hardly examined so far, such as Asia or Africa, where documented collections are scarce or working with skeletal remains is more difficult for international researchers.

Acknowledgements

We would like to thank Dr. José Antonio Sánchez and his team for allowing us access to the collection housed by the School of Legal Medicine at the Faculty of Medicine of the Complutense University of Madrid (Madrid, Spain).

Declarations

Ethical approval

N/A.
N/A.

Competing interests

The authors have no competing interests to declare that are relevant to the content of this article.

Conflict of interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Research involving human participant and/or animals

N/A.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Download
Titel
Application of DSP2 for biological sex estimation in a Spanish sample: analysis based on sex and side
Verfasst von
Marta San-Millán
Varsha Warrier
Anna Carrera
Francisco Reina
Publikationsdatum
15.11.2024
Verlag
Springer Berlin Heidelberg
Erschienen in
International Journal of Legal Medicine / Ausgabe 2/2025
Print ISSN: 0937-9827
Elektronische ISSN: 1437-1596
DOI
https://doi.org/10.1007/s00414-024-03358-1

Electronic supplementary material

Below is the link to the electronic supplementary material.
1.
Zurück zum Zitat Krishan K, Chatterjee PM, Kanchan T et al (2016) A review of sex estimation techniques during examination of skeletal remains in forensic anthropology casework. Forensic Sci Int 261. https://doi.org/10.1016/j.forsciint.2016.02.007. :165.e1-165.e8
2.
Zurück zum Zitat Buikstra J, Ubelaker D (1994) Standards for data collection from human skeletal remains. Ark Archaeol Surv Res Ser 44:44
3.
Zurück zum Zitat Ferembach D, Schwidetzky I, Stoukal M (1980) Recomendations for age and sex diagnosis of skeletons. J Hum Evol 9:517–549CrossRef
4.
Zurück zum Zitat Ubelaker DH (1999) Human Skeletal Remains: Excavation, Analysis, Interpretation. Washington
5.
Zurück zum Zitat White TD, Folkens PA (2005) The Human Bone Manual. Amsterdam; Boston
6.
Zurück zum Zitat Scheuer L (2002) Application of osteology to forensic medicine. Clin Anat 15:297–312. https://doi.org/10.1002/ca.10028CrossRefPubMed
7.
Zurück zum Zitat Bruzek J (2002) A method for visual determination of sex, using the human hip bone. Am J Phys Anthropol 117:157–168. https://doi.org/10.1002/ajpa.10012CrossRefPubMed
8.
Zurück zum Zitat Christensen AM, Passalacqua NV, Bartelink EJ (2019) Forensic Anthropology: current methods and practice. Academic
9.
Zurück zum Zitat Klales AR (2020) Chap. 2 - Practitioner preferences for sex estimation from human skeletal remains. In: Klales AR (ed) Sex Estimation of the Human Skeleton. Academic Press, pp 11–23
10.
Zurück zum Zitat Murail P, Bruzek J, Houët F, Cunha E (2005) DSP: a tool for probabilistic sex diagnosis using worldwide variability in hip-bone measurements. Bull Mém Société Anthropol Paris 17:167–176. https://doi.org/10.4000/bmsap.1157CrossRef
11.
Zurück zum Zitat Brůžek J, Santos F, Dutailly B et al (2017) Validation and reliability of the sex estimation of the human os coxae using freely available DSP2 software for bioarchaeology and forensic anthropology. Am J Phys Anthropol 164:440–449. https://doi.org/10.1002/ajpa.23282CrossRefPubMed
12.
Zurück zum Zitat Quatrehomme G, Radoman I, Nogueira L et al (2017) Sex determination using the DSP (probabilistic sex diagnosis) method on the coxal bone: efficiency of method according to number of available variables. Forensic Sci Int 272:190–193. https://doi.org/10.1016/j.forsciint.2016.10.020CrossRefPubMed
13.
Zurück zum Zitat Kranioti EF, Šťovíčková L, Karell MA, Brůžek J (2019) Sex estimation of os coxae using DSP2 software: a validation study of a Greek sample. Forensic Sci Int 297. https://doi.org/10.1016/j.forsciint.2019.02.011. :371.e1-371.e6
14.
Zurück zum Zitat Sánchez-Mejorada G, Gómez-Valdés J, Herrera P et al (2011) Valoración Del método de Diagnóstico sexual Probabilístico (dsp) en una colección osteológica mexicana. Estud Antropol Biológica 15. https://doi.org/10.22201/iia.14055066p.2011.42780
15.
Zurück zum Zitat De Almeida SM, De Carvalho MVD, De Lyra Menezes MCT et al (2020) Validation of the DSP2 Tool in a contemporary identified skeletal Collection from Northeastern Brazil. Adv Anthropol 10:169–180. https://doi.org/10.4236/aa.2020.102010CrossRef
16.
Zurück zum Zitat Rodrigo de Oliveira Lopes A, Silva EML, da Nascimento MM S, et al (2024) DSP2 for sex determination of miscegenated contemporary hip bones. Anat Histol Embryol 53:e12979. https://doi.org/10.1111/ahe.12979CrossRef
17.
Zurück zum Zitat Salles Machado MP, Costa ST, Freire AR et al (2018) Application and validation of Diagnose Sexuelle Probabiliste V2 tool in a miscegenated population. Forensic Sci Int 290. https://doi.org/10.1016/j.forsciint.2018.06.043. :351.e1-351.e5
18.
Zurück zum Zitat Chapman T, Lefevre P, Semal P et al (2014) Sex determination using the probabilistic sex diagnosis (DSP: diagnose Sexuelle Probabiliste) tool in a virtual environment. Forensic Sci Int 234:189e1–189e8. https://doi.org/10.1016/j.forsciint.2013.10.037CrossRef
19.
Zurück zum Zitat Mestekova S, Bruzek J, Veleminska J, Chaumoitre K (2015) A test of the DSP sexing method on CT images from a modern French sample. J Forensic Sci 60:1295–1299. https://doi.org/10.1111/1556-4029.12817CrossRefPubMed
20.
Zurück zum Zitat Rodriguez Paz A, Banner J, Villa C (2019) Validity of the probabilistic sex diagnosis method (DSP) on 3D CT-scans from modern Danish population. Rev Médecine Légale 10:43–49. https://doi.org/10.1016/j.medleg.2018.08.002CrossRef
21.
Zurück zum Zitat Rmoutilová R, Brůžek J, Gómez-Olivencia A et al (2024) Sex estimation of the adult Neandertal Regourdou 1 (Montignac, France): implications for sexing human fossil remains. J Hum Evol 189:103470. https://doi.org/10.1016/j.jhevol.2023.103470CrossRefPubMed
22.
Zurück zum Zitat Chapman T, Tilleux C, Polet C et al (2020) Validating the probabilistic sex diagnosis (DSP) method with a special test case on pre-columbian mummies (including the famous Rascar Capac). J Archaeol Sci Rep 30:102250. https://doi.org/10.1016/j.jasrep.2020.102250CrossRef
23.
Zurück zum Zitat Villotte S, Santos F, Courtaud P (2015) In situ study of the Gravettian individual from Cussac cave, locus 2 (Dordogne, France). Am J Phys Anthropol 158:759–768. https://doi.org/10.1002/ajpa.22831CrossRefPubMed
24.
Zurück zum Zitat Oh KC, Hwang T, Choi GO et al (2022) Evaluation through the Use of DSP2 Program for Sex Estimation by Measuring Human Hip bones in a Joseon Dynasty Bone Collection. Anat Biol Anthropol 35:9–19. https://doi.org/10.11637/aba.2022.35.1.9CrossRef
25.
Zurück zum Zitat Jerković I, Bašić Ž, Kružić I, Anđelinović Š (2018) Creating reference data on sex for ancient populations using the probabilistic sex diagnosis method: a validation test using the results of aDNA analysis. J Archaeol Sci 94:44–50. https://doi.org/10.1016/j.jas.2018.04.007CrossRef
26.
Zurück zum Zitat Villoria Rojas C, Mata Tutor P, Labajo González E et al (2023) The identified skeletal Collection of the School of Legal Medicine: a contemporary osteological collection housed in Universidad Complutense De Madrid, Spain. Int J Legal Med. https://doi.org/10.1007/s00414-023-03047-5CrossRefPubMedPubMedCentral
27.
Zurück zum Zitat Bräuer G (1988) Osteometrie. Anthropologie, handbuch des vergleichenden biologie des menschen, Knussmann. Gustav Fischer, Stuttgart, pp 160–232
28.
Zurück zum Zitat Gaillard J (1960) Détermination sexuelle d’un os coxal fragmentaire. Bull Mém Société Anthropol Paris 1:255–267. https://doi.org/10.3406/bmsap.1960.1145CrossRef
29.
Zurück zum Zitat Schulter-Ellis FP, Schmidt DJ, Hayek L-A, Craig J (1983) Determination of sex with a Discriminant Analysis of New Pelvic Bone measurements: part I. J Forensic Sci 28:169–180. https://doi.org/10.1520/JFS12249JCrossRefPubMed
30.
Zurück zum Zitat Daniel WW (1998) Biostatistics: A Foundation for Analysis in the Health Sciences, 7th edn. Wiley
31.
Zurück zum Zitat Koo TK, Li MY (2016) A Guideline of selecting and reporting Intraclass correlation coefficients for Reliability Research. J Chiropr Med 15:155–163. https://doi.org/10.1016/j.jcm.2016.02.012CrossRefPubMedPubMedCentral
32.
Zurück zum Zitat Amores-Ampuero A (2017) Sexual dimorphism in base of skull. Anthropol Anz 74:9–14. https://doi.org/10.1127/anthranz/2017/0603CrossRefPubMed
33.
Zurück zum Zitat Daniele G, Matilde S-SA, María M et al (2020) Sex estimation by tooth dimension in a contemporary Spanish population. Forensic Sci Int 317:110549. https://doi.org/10.1016/j.forsciint.2020.110549CrossRefPubMed
34.
Zurück zum Zitat Viciano J, López-Lázaro S, Alemán I (2013) Sex estimation based on deciduous and permanent dentition in a contemporary Spanish population. Am J Phys Anthropol 152:31–43. https://doi.org/10.1002/ajpa.22324CrossRefPubMed
35.
Zurück zum Zitat Alcina M, Rissech C, Clavero A, Turbón D (2015) Sexual dimorphism of the clavicle in a modern Spanish sample. Eur J Anat 19:73–83
36.
Zurück zum Zitat Ruiz Mediavilla E, Pérez B, Labajo González E et al (2016) Determining sex with the clavicle in a contemporary Spanish reference collection: a study on 3D images. Forensic Sci Int 261. https://doi.org/10.1016/j.forsciint.2016.01.029. :163.e1-163.e10
37.
Zurück zum Zitat Ruiz Mediavilla E, Labajo González E, Perea Pérez B et al (2017) Sex determination by bone volume in Spanish population: a study on 3D images of talus, radius, clavicle and patella. Rev Médecine Légale 8:188. https://doi.org/10.1016/j.medleg.2017.10.027CrossRef
38.
Zurück zum Zitat García-Parra P, Pérez Fernández Á, Djorojevic M et al (2014) Sexual dimorphism of human sternum in a contemporary Spanish population. Forensic Sci Int 244. https://doi.org/10.1016/j.forsciint.2014.06.019. :313.e1-313.e9
39.
Zurück zum Zitat Macaluso PJ, Rico A, Santos M, Lucena J (2012) Osteometric sex discrimination from the sternal extremity of the fourth rib in a recent forensic sample from Southwestern Spain. Forensic Sci Int 223. https://doi.org/10.1016/j.forsciint.2012.09.007. :375.e1-375.e5
40.
Zurück zum Zitat Partido Navadijo M, Fombuena Zapata I, Borja Miranda EA, Alemán Aguilera I (2021) Discriminant functions for sex estimation using the rib necks in a Spanish population. Int J Legal Med 135:1055–1065. https://doi.org/10.1007/s00414-021-02537-8CrossRefPubMed
41.
Zurück zum Zitat Amores A, Botella MC, Alemán I (2014) Sexual dimorphism in the 7th cervical and 12th thoracic vertebrae from a Mediterranean Population. J Forensic Sci 59:301–305. https://doi.org/10.1111/1556-4029.12320CrossRefPubMed
42.
Zurück zum Zitat Azofra-Monge A, Alemán Aguilera I (2020) Morphometric research and sex estimation of lumbar vertebrae in a contemporary Spanish population. Forensic Sci Med Pathol 16:216–225. https://doi.org/10.1007/s12024-020-00231-6CrossRefPubMed
43.
Zurück zum Zitat Gama I, Navega D, Cunha E (2015) Sex estimation using the second cervical vertebra: a morphometric analysis in a documented Portuguese skeletal sample. Int J Legal Med 129:365–372. https://doi.org/10.1007/s00414-014-1083-0CrossRefPubMed
44.
Zurück zum Zitat Gaya-Sancho B, Alemán Aguilera I, Navarro-Muñoz JJ, Botella López M (2018) Sex determination in a Spanish population based on sacrum. J Forensic Leg Med 60:45–49. https://doi.org/10.1016/j.jflm.2018.10.001CrossRefPubMed
45.
Zurück zum Zitat Ruiz Mediavilla E, Perea Pérez B, Labajo González E et al (2012) Determining sex by bone volume from 3D images: discriminating analysis of the tali and radii in a contemporary Spanish reference collection. Int J Legal Med 126:623–631. https://doi.org/10.1007/s00414-012-0715-5CrossRefPubMed
46.
Zurück zum Zitat Mastrangelo P, De Luca S, Alemán I, Botella MC (2011) Sex assessment from the carpals bones: discriminant function analysis in a 20th century Spanish sample. Forensic Sci Int 206. https://doi.org/10.1016/j.forsciint.2011.01.007. :216.e1-216.e10
47.
Zurück zum Zitat Clavero A, Salicrú M, Turbón D (2015) Sex prediction from the femur and hip bone using a sample of CT images from a Spanish population. Int J Legal Med 129:373–383. https://doi.org/10.1007/s00414-014-1069-yCrossRefPubMed
48.
Zurück zum Zitat Sobreira LB, Cunha E, Curate F (2023) Biological sex estimation with femoral dimensions: a study of an adult sample from the osteological collection of Granada (Spain). Aust J Forensic Sci 0:1–12. https://doi.org/10.1080/00450618.2023.2270648CrossRef
49.
Zurück zum Zitat Peckmann TR, Meek S, Dilkie N, Rozendaal A (2016) Determination of sex from the patella in a contemporary Spanish population. J Forensic Leg Med 44:84–91. https://doi.org/10.1016/j.jflm.2016.09.007CrossRefPubMed
50.
Zurück zum Zitat Garcia S (2012) Is the circumference at the nutrient foramen of the tibia of value to sex determination on human osteological collections? Testing a new method. Int J Osteoarchaeol 22:361–365. https://doi.org/10.1002/oa.1202CrossRef
51.
Zurück zum Zitat Kranioti EF, Apostol MA (2015) Sexual dimorphism of the tibia in contemporary greeks, italians, and Spanish: forensic implications. Int J Legal Med 129:357–363. https://doi.org/10.1007/s00414-014-1045-6CrossRefPubMed
52.
Zurück zum Zitat Saldías E, Malgosa A, Jordana X, Isidro A (2016) Sex estimation from the navicular bone in Spanish contemporary skeletal collections. Forensic Sci Int 267. https://doi.org/10.1016/j.forsciint.2016.08.002. :229.e1-229.e6
53.
Zurück zum Zitat Barrio PA, Trancho GJ, Sánchez JA (2006) Metacarpal sexual determination in a Spanish Population. J Forensic Sci 51:990–995. https://doi.org/10.1111/j.1556-4029.2006.00237.xCrossRefPubMed
54.
Zurück zum Zitat Djorojevic M, Roldán C, García-Parra P et al (2014) Morphometric sex estimation from 3D computed tomography os coxae model and its validation in skeletal remains. Int J Legal Med 128:879–888. https://doi.org/10.1007/s00414-014-1033-xCrossRefPubMed
55.
Zurück zum Zitat Brůžek J, Murail P, Houët F, Cleuvenot E (1994) Inter- and Intra-observer Error in pelvic measurements and its implication for the methods of sex determination. Anthropol 1962- 32:215–223
56.
Zurück zum Zitat Vacca E, Di Vella G (2012) Metric characterization of the human coxal bone on a recent Italian sample and multivariate discriminant analysis to determine sex. Forensic Sci Int 222. https://doi.org/10.1016/j.forsciint.2012.06.014. :401.e1-401.e9
57.
Zurück zum Zitat Avent PR, Hughes CE, Garvin HM (2022) Applying posterior probability informed thresholds to traditional cranial trait sex estimation methods. J Forensic Sci 67(2):440–449. https://doi.org/10.1111/1556-4029.14947CrossRefPubMed
58.
Zurück zum Zitat Pilmann Kotěrová A, Santos F, Bejdová Š et al (2024) Prioritizing a high posterior probability threshold leading to low error rate over high classification accuracy: the validity of MorphoPASSE software for cranial morphological sex estimation in a contemporary population. Int J Legal Med 138:1759–1768. https://doi.org/10.1007/s00414-024-03215-1CrossRefPubMed
59.
Zurück zum Zitat Fily M, Jaroslav B, Cunha E, Ludes B (2000) Researching ambiguous sex cases in ancient skeletons of the series of Coimbra (Portugal). Prog Forensic Genet 8:558–560
60.
Zurück zum Zitat Decker SJ, Davy-Jow SL, Ford JM, Hilbelink DR (2011) Virtual determination of sex: Metric and nonmetric traits of the adult pelvis from 3D computed tomography Models*†. J Forensic Sci 56:1107–1114. https://doi.org/10.1111/j.1556-4029.2011.01803.xCrossRefPubMed
61.
Zurück zum Zitat Gonzalez PN, Bernal V, Perez SI (2009) Geometric morphometric approach to sex estimation of human pelvis. Forensic Sci Int 189:68–74. https://doi.org/10.1016/j.forsciint.2009.04.012CrossRefPubMed
62.
Zurück zum Zitat Benazzi S, Maestri C, Parisini S et al (2008) Sex assessment from the acetabular rim by means of image analysis. Forensic Sci Int 180. https://doi.org/10.1016/j.forsciint.2008.06.007. :58.e1-58.e3
63.
Zurück zum Zitat Karakas HM, Harma A, Alicioglu B (2013) The subpubic angle in sex determination: anthropometric measurements and analyses on Anatolian caucasians using multidetector computed tomography datasets. J Forensic Leg Med 20:1004–1009. https://doi.org/10.1016/j.jflm.2013.08.013CrossRefPubMed
64.
Zurück zum Zitat Steyn M, Patriquin ML (2009) Osteometric sex determination from the pelvis—does population specificity matter? Forensic Sci Int 191. https://doi.org/10.1016/j.forsciint.2009.07.009. :113.e1-113.e5
65.
Zurück zum Zitat Betti L (2014) Sexual dimorphism in the size and shape of the os coxae and the effects of microevolutionary processes. Am J Phys Anthropol 153:167–177. https://doi.org/10.1002/ajpa.22410CrossRefPubMed
66.
Zurück zum Zitat Bruzek J, Murail P (2006) Methodology and reliability of sex determination from the Skeleton. In: Schmitt A, Cunha E, Pinheiro J (eds) Forensic Anthropology and Medicine: Complementary sciences from Recovery to cause of death. Humana, Totowa, NJ, pp 225–242CrossRef
67.
Zurück zum Zitat Hager LD (1989) The evolution of sex differences in the Hominid Bony Pelvis. University of California, Berkeley
68.
Zurück zum Zitat Hager LD (1996) Sex differences in the sciatic notch of great apes and modern humans. Am J Phys Anthropol 99(199602):287–300. https://doi.org/10.1002/(SICI)1096-8644. ::AID-AJPA6>3.0.CO;2-WCrossRefPubMed
69.
Zurück zum Zitat Rosenberg K, Trevathan W (2002) Birth, obstetrics and human evolution. BJOG Int J Obstet Gynaecol 109:1199–1206. https://doi.org/10.1046/j.1471-0528.2002.00010.xCrossRef
70.
Zurück zum Zitat Oelze VM, Koch JK, Kupke K et al (2012) Multi-isotopic analysis reveals individual mobility and diet at the early iron age monumental tumulus of magdalenenberg, Germany. Am J Phys Anthropol 148:406–421. https://doi.org/10.1002/ajpa.22063CrossRefPubMed
71.
Zurück zum Zitat Quintelier K (2009) Calcified uterine leiomyomata from a post-medieval nunnery in Brussels, Belgium. Int J Osteoarchaeol 19:436–442. https://doi.org/10.1002/oa.971CrossRef
72.
Zurück zum Zitat Scorrano G, Viva S, Pinotti T et al (2022) Bioarchaeological and palaeogenomic portrait of two pompeians that died during the eruption of Vesuvius in 79 AD. Sci Rep 12:6468. https://doi.org/10.1038/s41598-022-10899-1CrossRefPubMedPubMedCentral

Neu im Fachgebiet Rechtsmedizin

S2k-Leitlinie Früher Schwangerschaftsverlust im 1. Trimenon

Im Jahr 2025 wurde die S2k-Leitlinie Früher Schwangerschaftsverlust im 1. Trimenon veröffentlicht. In dieser Leitlinie werden sowohl für gestörte Frühgraviditäten als auch Schwangerschaften unklarer Lokalisation mit daraus resultierendem Abort …

Pädiatrische Lymphome: Herausforderungen in der Diagnostik

Lymphome im Kindesalter sind selten – und oft schwer einzuordnen. Die aktuellen Klassifikationen sowie die erstmals erschienene WHO-Klassifikationen unterstützen bei der Einteilung. In der dieser Übersicht werden die aktuellen Klassifikationen, Biologie und Diagnostik pädiatrischer Lymphome mit Fokus auf seltene indolente Entitäten sowie reaktive, Lymphom-imitierende Läsionen vorgestellt.

Protein kinase-related tumors in the pediatric population

  • Open Access
  • Schwerpunkt: Kinderpathologie: Von früher Plazenta bis Neoplasien

Advanced and widespread molecular techniques have deepened our understanding of mesenchymal lesions, revealing considerable overlap among morphologically defined entities now known to be related to protein kinases (PKs). This paradigm shift is …

Seltene kindliche benigne Tumoren/Läsionen im Kopfbereich

Benigne Tumoren und Läsionen im Kopfbereich bei Kindern sind selten und können eine diagnostische Herausforderung sein. Im Rahmen dieses Artikels werden ausgewählte seltene kindliche, benigne Läsionen im Kopfbereich vorgestellt mit dem Ziel, die …

Bildnachweise
Histologie einer Anaplastische Lymphomkinase mit großzellig-anaplastisches Lymphom/© Bosch-Schips J et al. / all rights reserved Springer Medizin Verlag GmbH