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Erschienen in: International Journal of Mental Health Systems 1/2016

Open Access 01.12.2016 | Research

Comorbidity of depression and diabetes: an application of biopsychosocial model

verfasst von: Tesfa Dejenie Habtewold, Md. Atiqul Islam, Yosef Tsige Radie, Balewgizie Sileshi Tegegne

Erschienen in: International Journal of Mental Health Systems | Ausgabe 1/2016

Abstract

Background

Type 2 diabetes (T2D) is one of the most psychologically demanding chronic medical illness in adult. Comorbidity between diabetes and depression is quite common, but most studies were based on developed country sample. Limited data exists to document biopsychosocial predictors of depressive symptoms in Ethiopian patients. Therefore, the aim of the study was to describe the association of depressive symptoms and T2D and explore the potential underlying associated biopsychosocial risk factors.

Methods

Institution based cross-sectional study was conducted on 276 patient with T2D at diabetic clinic, Black Lion General Specialized Hospital in Ethiopia. Patients were selected using systematic random sampling technique. Depressive symptoms score, which constructed from a validated nine-item Patient Health Questionnaire (PHQ-9), was an outcome variable. Finally, significant associated factors were identified using multiple linear regression analysis with backward elimination procedure. Statistical Package for Social Science (SPSS) version 22.0 (IBM SPSS Corp.) was used to perform all analysis.

Results

Total of 264 patient data was analyzed with 95.7% response rate. Patients mean (SD) current age and age at diagnosis was 55.9 (10.9) and 43.9 (10.9) years, respectively. Patients waist circumference (mean ± SD) was 98.9 ± 11.1 cm. The average PHQ-9 score was 4.9 (SD 4.1) and fasting blood glucose was 166.4 (SD 73.2). Marital status (divorced), occupation (housewife), diabetic complication (nephropathy), negative life event in the last six months, and poor social support significantly associated with increased mean PHQ-9 score after adjustment for covariates. Whereas not fearing diabetic-related complication and death significantly lower mean PHQ-9 score.

Conclusion

Biopsychosocial variables including marital status, negative life event in the last 6 months, occupation, diabetic complication, and poor social support significantly increase average depressive symptoms score. Evidence-based intervention focusing on these identified biopsychosocial factors are necessary to prevent the development of depressive symptoms.

Background

Diabetes mellitus (DM) has been affecting millions of people from all over the world. In 2013, 382 million people had diabetes; this estimate is expected to rise to 592 million by 2035 [1, 2]. More than 77% of morbidity and 88% of mortality due to DM occur in low and middle-income countries. In Ethiopia, the prevalence of diabetes was 0.34–5.0% [3, 4]. During the last decades, the comorbidity of mental disorders with chronic health conditions have emerged as a topic of considerable clinical and policy interest. Due to complex nature of disease pathophysiology, cause, and treatment, type 2 diabetes (T2D) is considered one of the most psychologically demanding chronic medical illness in an adult patient [5, 6]. In spite of this, up to 45% of cases of comorbid mental disorder and severe psychological distress were poorly identified and inadequately treated among patients with diabetes in sub-Saharan Africa [7, 8]. The prevalence of psychiatric disorders in diabetic patients may reach 84% for mood disorders and 80% for anxiety disorders [9, 10]. Based on a study report by Ana Claudia and colleagues the most prevalent comorbid disorders were generalized anxiety disorder (21%), dysthymia (15%), social phobia (7%), lifelong depression (3.5%), panic disorder (2.5%), and risk of suicide (2%) [10]. Depression was among the most common neuropsychiatric disorders in patients with T2D [8].
Thomas Willis, British physician, recognized the association between depression and diabetes since 17th century [11]. Epidemiologically, one in every four patient with T2D develops clinically significant depression [12]. The estimated lifetime prevalence of depression was higher in women (21%) [13]. The prevalence of depression in T2D patient was 5.5–49.6% [10, 1422]. Even though most studies was on Western samples, there have been emerging studies in developing countries including Ethiopia [16, 2325]. A cross-sectional study by Erkie et al. described depression was diagnosed in 64.8% of T2D outpatient [23]. The exact mechanisms of relationship are elusive, and models for the associated factors are multidimensional.
Engel’s [26] biopsychosocial model of health and illness is a model for clinical practice and research for psychologists, nurses, physicians, and social workers [27]. American Psychiatric Association and American Board of Psychiatry and Neurology have officially approved Engel’s model [28, 29]. According to Engel’s model any disease such as depression [3033] caused by biological (physiological or genetic predispositions), psychological (health beliefs and lifestyle) and social factors (family relationships, socioeconomic status, and social support). The model reveals the interaction of this factor to create patient’s state of mind and body [34, 35] (Fig. 1).
T2D patients were poorly diagnosed and inadequately treated in sub-Saharan Africa [8]. In general, the data is limited, and the conclusion seems inadequate to identify biopsychosocial risk factors of depressive symptoms in Ethiopian diabetic patients. In the present study, we aimed to describe the association of depressive symptoms and T2D, and explore the potential underlying associated risk factors.

Methods

Study design and population

We conducted an institution based cross-sectional study among T2D outpatients on regular follow-up at Black Lion General Specialized Hospital from February to April 2013.

Determinants and covariables

The outcome variable was depressive symptoms score. The explanatory variables were biological factors: age, sex, comorbid disease, diabetic complication, diabetic treatment, fasting blood glucose, body mass index; psychological factors: unemployment, financial stress, negative life event, polypharmacy, smoking, lack of regular physical activity, perceived fear of complication and death, perceived high healthcare cost; and social factors: socioeconomic status, educational status, marital status, major family conflict, poor social support. We defined polypharmacy as taking greater than or equal to four prescribed medications per day. Poor social support was defined as lack of support or care from the family, friends, and neighbors. Another studied factor was, which referred to an event such as accident and death in the last six months that leads to a feeling of stress or anxiety, negative life event. Perceived fear of complication and death was defined as individual feeling or opinion about his/her illness and related complication. Perceived high healthcare cost was defined as personal feeling or idea about the expense of diabetes treatment. Physical activity was defined as doing any aerobic exercise 3–5 times per week at least for 30 min.

Sampling and data collection

Patients were chosen based on three criteria: T2D diagnosis at least for one year, age ≥20 years old, capable of independent communication, and signed written informed consent. Patients treated for depression, or other psychological illnesses (e.g. anxiety or personality disorders) were excluded. Systematic random sampling technique was used to reach individual patients. The data was collected by two trained Nurses from every three patients (sampling interval/k/ = 3). All biological (physiological) data was collected from patients’ medical chart. Face-to-face interview was conducted in the treating private clinics to collect psychological and social data. Twelve patients refused to take part because of lack of interest to participate and a shortage of time. In total 264 cases were included in the final analysis.

Measuring depressive symptoms

Depression, which refers to symptoms experienced during the last two weeks, was measured by Patient Health Questionnaire (PHQ-9) [36, 37]. The PHQ-9 includes nine items with individual score ranges from 0 (not at all) to 3 (nearly every day). The total sum score ranging from 0 to 27. PHQ-9 scores with cut-off point 5, 10, 15 and 20 represent mild, moderate, moderately severe, and severe depression, respectively [36]. In our study, T2D patients’ depression status was measured by administering a validated Ethiopian version PHQ-9 questionnaire. Gelaye and colleagues showed PHQ-9 internal reliability of 0.81, test re-test reliability of 0.92, sensitivity of 86%, and specificity of 67% [38].

Statistical analysis

First of all, four cases were not included in our analysis because of outlying PHQ-9 score (≥20). Descriptive statistics including mean, standard deviation, percentage, and cross-tabulation was performed for all patient parameters. Univariate linear regression analysis was performed per each biopsychosocial variable. The full model of multiple linear regression included all significant variables. Finally, significantly associated factors were identified by backward elimination procedure. QQ-plot, histogram and scatter plot of ‘Standardized residuals’ against ‘Standardized predicted values’ were used to check the assumptions of linearity of relationships, normal distribution and homoscedasticity of residuals for the final model. Two-tailed test at 5% level of significance was used for all association test. Statistical Package for Social Science (SPSS) version 22.0 (IBM SPSS Corp.) was used to perform all analysis. The study was adherent to the STROBE criteria.

Results

Biopsychosocial characteristics of patients

Total of 264 patient data was analyzed with 95.7% response rate. Patients mean (SD) current age and age at diagnosis was 55.9 (10.9) and 43.9 (10.9) years, respectively. Also, patients waist circumference (mean ± SD) was 98.9 ± 11.1 cm while patients family median monthly income was 750 Ethiopian Birr (651–1400). The average PHQ-9 score was 4.9 (SD 4.1) and fasting blood glucose was 166.4 (SD 73.2). The mean ± SD of PHQ-9 score was 6 ± 4.7 in female, 7.3 ± 5.7 in divorced, 6.6 ± 4.5 in educational level of grade 1–8, and 6.77 ± 5.3 in housewife patient. The mean ± SD of number of comorbid diseases and body mass index was 1.1 ± 0.9 and 25.4 ± 3.7, respectively (Table 1).
Table 1
Distribution of patients PHQ-9 score and fasting blood glucose by biopsychosocial characteristics of patients
Variable
Categories
n (%)
PHQ-9 score mean (± SD)
Fasting blood sugar mean (±SD)
Gender, female
140 (53.0)
6.0 (4.77)
181.30 (79.94)
Residence, Addis Ababa
228 (86.4)
5.07 (4.35)
166.13 (71.78)
Marital status
Married
183 (69.3)
4.68 (4.17)
164.4 (70.67)
Divorced
24 (9.1)
7.3 (5.75)
188.94 (94.31)
Widowed
48 (18.2)
5.92 (4.73)
162.04 (66.48)
Religion
Orthodox christian
213 (80.7)
5.48 (4.74)
167.64 (72.76)
Muslim
24 (9.1)
3.71 (3.14)
170.04 (92.81)
Other religion
5 (1.9)
4.67 (4.04)
159.63 (61.18)
Ethnicity
Amhara
151 (57.2)
5.23 (4.71)
168.71 (74.05)
Oromo
40 (15.2)
5.8 (4.54)
165.65 (77.42)
Others
19 (7.2)
4.93 (4.33)
164.36 (70.94)
Educational status
No formal education
51 (19.4)
6.1 (5.17)
179.57 (81.79)
Grade 1–8
16 (6.1)
6.63 (4.53)
171.11 (78.94)
Grade 9–12
59 (22.3)
4.42 (4.08)
165.66 (63.11)
College/university
89 (33.7)
4.26 (4.25)
157.81 (70.59)
Occupation
Civil servant
47 (17.8)
4.74 (4.71)
172.51 (59.36)
House wife
47 (17.8)
6.77 (5.26)
183.45 (71.56)
Private worker
38 (14.4)
4.29 (3.84)
162.95 (93.59)
Pensioned
58 (22.0)
4.69 (4.48)
142.0 (56.18)
No employment
48 (18.2)
5.85 (4.14)
172.9 (80.15)
Others
16 (6.1)
4.81 (4.53)
178.54 (79.98)
Diabetes treatment
Single insulin injection
108 (40.9)
5.78 (4.99)
162.44 (83.22)
Combined insulin injection
12 (4.5)
5.92 (5.14)
218.17 (104.57)
Insulin plus oral hypoglycemic
30 (11.4)
5.23 (3.61)
167.67 (58.89)
Oral hypoglycemic
114 (43.2)
4.65 (4.29)
165.85 (61.25)
Comorbid disease (N = 180)
Cardiovascular disease
141 (78.3)
5.57 (4.68)
162.81 (68.43)
Respiratory disease
17 (9.4)
5.41 (4.43)
151.53 (66.82)
Renal disease
13 (7.2)
5.54 (4.31)
158.46 (58.13)
Neurologic disease
4 (2.2)
6.75 (6.13)
131.5 (35.48)
Others comorbidity
80 (44.4)
6.04 (5.09)
174.59 (72.01)
Diabetic complication (N = 201)
Diabetic retinopathy
140 (69.7)
5.79 (4.67)
166.76 (70.51)
Diabetic nephropathy
69 (34.3)
7.09 (5.16)
176.43 (72.36)
Diabetic neuropathy
83 (41.3)
6.14 (4.59)
172.41 (81.17)
Sexual dysfunction
69 (34.3)
4.70 (4.77)
162.29 (69.88)
Physical disability
132 (50.0)
5.80 (4.68)
169.61 (75.71)
Poor social support
95 (37.4)
7.44 (5.03)
167.47 (82.95)
Negative life event
88 (34.6)
6.64 (4.93)
168.75 (84.38)
Physical activity
55 (22%)
3.80 (3.53)
165.98 (82.69)
Perceived fear of complication and death
178 (70.1)
5.78 (4.74)
167.24 (71.88)
Perceived high health care cost of diabetes
192 (75.6)
5.35 (4.75)
168.15 (75.95)
SD standard deviation

Univariate linear regression test of association

Patient mean PHQ-9 score was significantly increased by 1.4 (95% CI 0.4–2.4) in female, 2.2 (95% CI 0.7–3.7) in divorced, and 1.7 (95% CI 0.4–3.0) in housewife. One unit increase in number of comorbidities was associated with a 0.6 unit (p = 0.04) increase in PHQ-9 score. One unit increase in number of diabetic complication was associated with a 0.5 unit (p = 0.02) increase in PHQ-9 score. Increased age at diagnosis (i.e. late-onset diabetes), increased monthly family income, high educational status (college or university), doing physical activity and not fearing diabetes-related complication and death significantly lower mean PHQ-9 score (Table 2).
Table 2
Univariate linear regression test examining the association between biopsychosocial variables and PHQ-9 score of patients
Variables (reference category)
β (95% CI)
p value
Current age
−0.03 (−0.08, 0.02)
0.21
Age at diagnosis
−0.05 (−0.1, −0.001)
0.04
Female gender (male)
1.4 (0.4, 2.4)
0.01
Addis Ababa residence (outside Addis Ababa)
−0.5 (−2.0, 1.0)
0.54
Monthly family income (ETB)
−0.001 (−0.001, −0.0002)
<0.001
Marital status (married)
 Divorced
2.2 (0.7, 3.7)
0.01
 Widowed
0.3 (−1.1, 1.6)
0.70
Religion (orthodox christian)
 Muslim
−1.4 (−3.1, 0.3)
0.11
 Other religion
−0.4 (−2.0, 1.3)
0.67
Ethnicity (others)
 Amhara
−0.2 (−1.2, 0.8)
0.67
 Oromo
1.0 (−0.4, 2.4)
0.17
Educational status (no formal education)
 Primary school (1–8)
1.8 (0.7, 3.0)
0.002
 Secondary school (9–12)
−0.7 (−1.9, 0.5)
0.23
 College/university
−1.4 (−2.4, −0.3)
0.01
Occupation (others)
 Civil servant
−0.7 (−2.0, 0.6)
0.28
 House wife
1.7 (0.4, 3.0)
0.01
 Private worker
−0.8 (−2.2, 0.6)
0.26
 Pensioned
−0.7 (−2.0, 0.5)
0.23
 No employment
1.1 (−0.7, 2.2)
0.10
Waist circumference
0.01 (−0.4, 0.1)
0.74
Duration of diabetes
0.03 (−0.03, 0.1)
0.35
Duration of diabetes treatment
0.03 (−0.04, 0.1)
0.36
Fasting blood glucose
0.01 (−0.001, 0.01)
0.09
Number of co-morbidity
0.6 (0.02, 1.1)
0.04
Number of prescribed medication administration per day
0.2 (−0.05, 0.4)
0.13
Number of diabetic complication
0.5 (0.1, 0.9)
0.02
Body mass index
0.1 (0.03, 0.3)
0.04
Combined insulin injection (single insulin injection)
1.0 (−1.9, 0.4)
0.42
Insulin injection plus oral hypoglycemic (single insulin injection)
0.3 (−1.3, 1.9)
0.72
Oral hypoglycemic agent (single insulin injection)
−0.9 (−2.0, 0.1)
0.08
Cardiovascular disease
0.5 (−0.5, 1.5)
0.33
Respiratory disease
0.5 (−1.6, 2.5)
0.66
Renal disease
0.6 (−1.7, 2.9)
0.62
Neurologic disease
1.8 (−2.3, 5.9)
0.39
Others comorbidity
0.7 (−0.4, 1.8)
0.22
Diabetic retinopathy
1.0 (0.02, 2.0)
0.04
Diabetic nephropathy
2.0 (0.8, 3.1)
0.001
Diabetic neuropathy
1.1 (0.03, 2.2)
0.04
Sexual dysfunction
−1.0 (−2.2, 0.1)
0.08
Physical disability
1.2 (0.2, 2.2)
0.02
Poor social support
3.1 (2.1, 4.1)
<0.001
Doing physical activity
−1.5 (−2.7, −0.3)
0.01
Fear of diabetic complication and death (no perception at all)
1.6 (0.6, 2.7)
0.003
Not fearing diabetic complication and death (no perception at all)
−2.0 (−3.1, −0.9)
<0.001
High health care cost (no perception at all)
0.4 (−0.7, 1.5)
0.50
Not high health care cost (no perception at all)
−0.7 (−2.0, 0.5)
0.26
Negative life event in the last 6 months
2.0 (0.9, 2.9)
<0.001
β regression coefficient; CI confidence interval

Multiple linear regression tests of association

All significant biopsychosocial variables, Table 3, in the final model together explained about 25.3% of the variability of patients PHQ-9 score. Divorce, housewife, diabetic nephropathy, negative life event, and poor social support were significant risk factors associated with increased PHQ-9 score after adjustment for covariates. However, not fearing diabetic-related complications and death significantly lower PHQ-9 score. Additional file 1: Table S1 presented all confounding factors.
Table 3
Multiple linear regression test examining the relation between different biopsychosocial associated factors and PHQ-9 score of patients with T2D mellitus
Variables
β (95% CI)
p value
t value
Divorce
2.0 (0.6, 3.4)
0.004
2.91
Negative life event in the last 6 months
1.3 (0.3, 2.2)
0.009
2.63
House wife
1.7 (0.5, 2.8)
0.005
2.80
Diabetic nephropathy
1.5 (0.4, 2.5)
0.005
2.80
Poor social support
2.4 (1.5, 3.4)
<0.001
5.07
Not fearing diabetic-related complications and death
−1.5 (−2.5, −0.5)
0.003
−2.97
β regression coefficient; CI confidence interval
The final model reasonably fulfilled three assumptions: linearity of relationship (Additional file 1: Figure S1), homoscedasticity (Additional file 1: Figure S2), and normal distribution (Additional file 1: Figure S3) assumptions. For further information, residual statistics table (Additional file 1: Table S2) accompanied as well.

Discussion

This study examined biopsychosocial factors associated with comorbid depression in patients with T2D.
In this study diabetic nephropathy, biologic factor consistent with other studies [39, 40], significantly increased the risk of depression. However, several other studies recognized gender [16, 17, 21, 4143], age [16, 17, 20, 44, 45], diabetic treatment [21, 46, 47], body mass index [21, 48], fasting plasma glucose [1719, 49, 50], poor diabetes mellitus control [15], number of comorbidities [21, 48, 51, 52], diabetic complications [16, 17, 53, 54], duration of diabetes [23, 45], age at diabetes diagnosis [55, 56], large waist circumference [39], diabetic retinopathy [40], diabetic neuropathy [39, 40, 57, 58], cardiovascular disease comorbidity [39, 40, 59, 60], sexual dysfunction [40] were physiologic (biologic) risk factors that significantly associated with depression.
In this study occupational status (housewife) and experiencing negative life events, psychological factors, significantly increased risk of depression in line with other earlier studies [39, 57, 61]. Interestingly, our final model uncovered not fearing diabetic related complications and death significantly lower risk of depression. On the other hand, depression was associated with diabetes treatment complexity [62], experienced loss of business or crop failure [16], unemployment [44, 47, 52], lack of regular physical activity [14, 21, 47], smoking [21, 48, 63], financial stress [39, 57, 61], poor quality of life [61, 64], and polypharmacy [39, 65].
Finally, we confirmed marital status (divorce) and poor social support, social factors similar to previous studies [19, 21, 57], significantly increased risk of depression. Contrariwise, urban residence [59], low socioeconomic status [19, 20, 42, 47, 66], lower educational status [23, 47, 49, 52], marital status [15, 17, 19, 21, 24, 44], major family conflicts and unavailability of food or medicines [16] were significant associated factors for depression.
Similar to previous studies [39, 58, 59, 6770], our final model proved risk of depression was not significantly associated with current age, sex, educational status, residence, ethnicity, socioeconomic status, poor body weight control, insulin treatment users, duration of diabetes, obesity, hypertensive disorder, and diabetic retinopathy. Recent studies [3942, 4749, 51, 66] found diabetic neuropathy, doing physical activity, diabetic retinopathy, educational status, perceived fear of diabetes-related death and complication, number of diabetic complication, being female, physical disability, increased body mass index, low monthly family income, age at diagnosis, and increased number of co-morbid disease significantly associated with depression. However, our study lacks to confirm this robust fact.
Most of these inconsistencies might be attributed to inadequacies in study design, implementation (i.e. data analysis and sample selection), interpretation (i.e. categorizing and using different cutoff point to diagnose depression), inadequately powered sample groups, and using different depression diagnostic tool. Using dichotomized PHQ-9 score as an outcome variable clearly causes loss of information, loss of power, bias, incomplete correction for confounding factors, and difficulty for robust replication of associated risk factors [7173]. Similarly, Olivier Naggara and colleagues argued dichotomization is unnecessary for statistical analysis, and continuous variable should be left alone in statistical model [74]. Researchers have used different cut-off point for dichotomizing PHQ-9 score [22, 59] that compromise replication for an unbiased view of the evidence from a particular study.
This study has important public health implication for health care practice in Black Lion General Specialized Hospital and another health facility, where clinician diagnosis of mental illness (depression) rate is low because of high patient load, lack of screening tool, role confusion, and lack of training. Another important barrier to the care of people with mental and physical health problem in lower and middle-income country is the lack of an integrated model for mental and medical health service [75]. We suggest physician or physiotherapist screen mental health and psychiatrist screen physical health of patient. Finally, clinicians should be aware of various factors and use biopsychosocial model to integrate their patient care.

Strengths and limitations

The strength of this study includes the use of PHQ-9 score as continuous outcome variable. Variables were defined based on Engel’s biopsychosocial model as well. However, this study has certain limitation. Most parameters estimated were biologic (physiologic) factors. This might underestimate the effect of psychological and social factors. Poor social support, which was identified as a highly significant associated factor, was assessed by a single item. Additionally, this study was conducted in one institution that might limit external validity of the finding. This study examined only the associations between the selected variables and PHQ-9 score. Lastly, the role of inflammation and genetic susceptibility for the emergence of depressive symptoms was not assessed.

Conclusions

In general biopsychosocial variables including marital status, negative life event in the last six months, occupational status, diabetic complication, and poor social support significantly increased risk of depression. Evidence-based intervention focusing on these identified biopsychosocial factors are necessary to prevent the development of depressive symptoms. Our study finding described the effect of various biopsychosocial factors on patient’s mood because depression-related factors frequently missed in people with diabetes [76]. This will improve evidence-based practice for comprehensive management physical and mental illness [77].

Authors’ contributions

TDH and YTR conceived and designed the study. TDH, MAI, and BST analyzed the data, interpreted the result and wrote the manuscript. All authors read and approved the final manuscript.

Acknowledgements

Our in-depth gratitude goes to Addis Ababa University for giving this chance and approval of the study too. Our sincerest thank goes to Dr. Behrooz Z. Alizadeh (Genetic Epidemiologist, Associate Professor, University Medical Center Groningen, the Netherlands) for his intellectual comment during manuscript writing. Data collectors and respondents were highly acknowledged for investing their precious time for collecting data and providing the necessary information. We would like to offer our great respect and appreciation to all our friends and senior instructors who gave us precious time for advice and comments during data entry and analysis.

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

All the relevant data was included in the article.
To conform the Declaration of Helsinki (1964) and Population Screening Act (WBO), Addis Ababa University Institutional Review Board approved the study. Participation was voluntary, and information was collected anonymously after obtaining written consent from each respondent. Confidentiality of patient data was ensured throughout the study.

Funding

This study was conducted in collaboration with Addis Ababa University. Every step of the project was followed by Addis Ababa University, centralized school of nursing and midwifery. The university has no role in designing, analysis and writing of the study. The researchers received no specific funding for this work.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
Literatur
1.
Zurück zum Zitat Harrison TA, Hindorff LA, Kim H, Wines RC, Bowen DJ, McGrath BB, et al. Family history of diabetes as a potential public health tool. Am J Prev Med. 2003;24(2):152–9.CrossRefPubMed Harrison TA, Hindorff LA, Kim H, Wines RC, Bowen DJ, McGrath BB, et al. Family history of diabetes as a potential public health tool. Am J Prev Med. 2003;24(2):152–9.CrossRefPubMed
2.
Zurück zum Zitat Guariguata L, Whiting D, Hambleton I, Beagley J, Linnenkamp U, Shaw J. Global estimates of diabetes prevalence for 2013 and projections for 2035. Diabetes Res Clin Pract. 2014;103(2):137–49.CrossRefPubMed Guariguata L, Whiting D, Hambleton I, Beagley J, Linnenkamp U, Shaw J. Global estimates of diabetes prevalence for 2013 and projections for 2035. Diabetes Res Clin Pract. 2014;103(2):137–49.CrossRefPubMed
3.
Zurück zum Zitat Kassahun T, Eshetie T, Gesesew H. Factors associated with glycemic control among adult patients with type 2 diabetes mellitus: a cross-sectional survey in Ethiopia. BMC Res Notes. 2016;9(1):78.CrossRefPubMedPubMedCentral Kassahun T, Eshetie T, Gesesew H. Factors associated with glycemic control among adult patients with type 2 diabetes mellitus: a cross-sectional survey in Ethiopia. BMC Res Notes. 2016;9(1):78.CrossRefPubMedPubMedCentral
4.
Zurück zum Zitat Habtewold TD, Tsega WD, Wale BY. Diabetes mellitus in outpatients in Debre Berhan referral hospital, Ethiopia. J Diabetes Res. 2016;2016:3571368.CrossRefPubMedPubMedCentral Habtewold TD, Tsega WD, Wale BY. Diabetes mellitus in outpatients in Debre Berhan referral hospital, Ethiopia. J Diabetes Res. 2016;2016:3571368.CrossRefPubMedPubMedCentral
5.
Zurück zum Zitat Kruse J, Schmitz N, Thefeld W, German National Health Interview and Examination Survey. On the association between diabetes and mental disorders in a community sample: results from the German National Health Interview and Examination Survey. Diabetes Care. 2003;26(6):1841–6.CrossRefPubMed Kruse J, Schmitz N, Thefeld W, German National Health Interview and Examination Survey. On the association between diabetes and mental disorders in a community sample: results from the German National Health Interview and Examination Survey. Diabetes Care. 2003;26(6):1841–6.CrossRefPubMed
6.
Zurück zum Zitat Chew BH, Vos R, Mohd-Sidik S, Rutten GE. Diabetes-related distress, depression and distress-depression among adults with type 2 diabetes mellitus in Malaysia. PLoS ONE. 2016;11(3):e0152095.CrossRefPubMedPubMedCentral Chew BH, Vos R, Mohd-Sidik S, Rutten GE. Diabetes-related distress, depression and distress-depression among adults with type 2 diabetes mellitus in Malaysia. PLoS ONE. 2016;11(3):e0152095.CrossRefPubMedPubMedCentral
8.
Zurück zum Zitat Akena D, Kadama P, Ashaba S, Akello C, Kwesiga B, Rejani L, et al. The association between depression, quality of life, and the health care expenditure of patients with diabetes mellitus in Uganda. J Affect Disord. 2015;15(174):7–12.CrossRef Akena D, Kadama P, Ashaba S, Akello C, Kwesiga B, Rejani L, et al. The association between depression, quality of life, and the health care expenditure of patients with diabetes mellitus in Uganda. J Affect Disord. 2015;15(174):7–12.CrossRef
9.
Zurück zum Zitat Chaudhry R, Mishra P, Mishra J, Parminder S, Mishra BP. Psychiatric morbidity among diabetic patients: a hospital-based study. Ind Psychiatry J. 2010;19(1):47–9.CrossRefPubMedPubMedCentral Chaudhry R, Mishra P, Mishra J, Parminder S, Mishra BP. Psychiatric morbidity among diabetic patients: a hospital-based study. Ind Psychiatry J. 2010;19(1):47–9.CrossRefPubMedPubMedCentral
10.
Zurück zum Zitat de Ornelas Maia AC, de Azevedo Braga A, Brouwers A, Nardi AE, Oliveira e Silva AC. Prevalence of psychiatric disorders in patients with diabetes types 1 and 2. Compr Psychiatry. 2012;53(8):1169–73.CrossRef de Ornelas Maia AC, de Azevedo Braga A, Brouwers A, Nardi AE, Oliveira e Silva AC. Prevalence of psychiatric disorders in patients with diabetes types 1 and 2. Compr Psychiatry. 2012;53(8):1169–73.CrossRef
11.
Zurück zum Zitat Moulton CD, Pickup JC, Ismail K. The link between depression and diabetes: the search for shared mechanisms. Lancet Diabetes Endocrinol. 2015;3(6):461–71.CrossRefPubMed Moulton CD, Pickup JC, Ismail K. The link between depression and diabetes: the search for shared mechanisms. Lancet Diabetes Endocrinol. 2015;3(6):461–71.CrossRefPubMed
12.
Zurück zum Zitat Semenkovich K, Brown ME, Svrakic DM, Lustman PJ. Depression in type 2 diabetes mellitus: prevalence, impact, and treatment. Drugs. 2015;75(6):577–87.CrossRefPubMed Semenkovich K, Brown ME, Svrakic DM, Lustman PJ. Depression in type 2 diabetes mellitus: prevalence, impact, and treatment. Drugs. 2015;75(6):577–87.CrossRefPubMed
13.
Zurück zum Zitat Snoek FJ, Bremmer MA, Hermanns N. Constructs of depression and distress in diabetes: time for an appraisal. Lancet Diabetes Endocrinol. 2015;3(6):450–60.CrossRefPubMed Snoek FJ, Bremmer MA, Hermanns N. Constructs of depression and distress in diabetes: time for an appraisal. Lancet Diabetes Endocrinol. 2015;3(6):450–60.CrossRefPubMed
15.
Zurück zum Zitat El Mahalli AA. Prevalence and predictors of depression among type 2 diabetes mellitus outpatients in Eastern Province, Saudi Arabia. Int J Health Sci (Qassim). 2015;9(2):119–26. El Mahalli AA. Prevalence and predictors of depression among type 2 diabetes mellitus outpatients in Eastern Province, Saudi Arabia. Int J Health Sci (Qassim). 2015;9(2):119–26.
16.
Zurück zum Zitat Islam SM, Rawal LB, Niessen LW. Prevalence of depression and its associated factors in patients with type 2 diabetes: a cross-sectional study in Dhaka, Bangladesh. Asian J Psychiatr. 2015;17:36–41.CrossRefPubMed Islam SM, Rawal LB, Niessen LW. Prevalence of depression and its associated factors in patients with type 2 diabetes: a cross-sectional study in Dhaka, Bangladesh. Asian J Psychiatr. 2015;17:36–41.CrossRefPubMed
17.
Zurück zum Zitat Rodriguez Calvin JL, Zapatero Gaviria A, Martin Rios MD. Prevalence of depression in type 2 diabetes mellitus. Rev Clin Esp. 2015;215(3):156–64.CrossRefPubMed Rodriguez Calvin JL, Zapatero Gaviria A, Martin Rios MD. Prevalence of depression in type 2 diabetes mellitus. Rev Clin Esp. 2015;215(3):156–64.CrossRefPubMed
18.
Zurück zum Zitat Wang L, Song R, Chen Z, Wang J, Ling F. Prevalence of depressive symptoms and factors associated with it in type 2 diabetic patients: a cross-sectional study in China. BMC Public Health. 2015;15:188.CrossRefPubMedPubMedCentral Wang L, Song R, Chen Z, Wang J, Ling F. Prevalence of depressive symptoms and factors associated with it in type 2 diabetic patients: a cross-sectional study in China. BMC Public Health. 2015;15:188.CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat Zhang W, Xu H, Zhao S, Yin S, Wang X, Guo J, et al. Prevalence and influencing factors of co-morbid depression in patients with type 2 diabetes mellitus: a General Hospital based study. Diabetol Metab Syndr. 2015;7:60 (eCollection 2015).CrossRefPubMedPubMedCentral Zhang W, Xu H, Zhao S, Yin S, Wang X, Guo J, et al. Prevalence and influencing factors of co-morbid depression in patients with type 2 diabetes mellitus: a General Hospital based study. Diabetol Metab Syndr. 2015;7:60 (eCollection 2015).CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Ganasegeran K, Renganathan P, Manaf RA, Al-Dubai SA. Factors associated with anxiety and depression among type 2 diabetes outpatients in Malaysia: a descriptive cross-sectional single-centre study. BMJ Open. 2014;4(4):e004794.CrossRefPubMedPubMedCentral Ganasegeran K, Renganathan P, Manaf RA, Al-Dubai SA. Factors associated with anxiety and depression among type 2 diabetes outpatients in Malaysia: a descriptive cross-sectional single-centre study. BMJ Open. 2014;4(4):e004794.CrossRefPubMedPubMedCentral
21.
Zurück zum Zitat Gorska-Ciebiada M, Saryusz-Wolska M, Ciebiada M, Loba J. Mild cognitive impairment and depressive symptoms in elderly patients with diabetes: prevalence, risk factors, and comorbidity. J Diabetes Res. 2014;2014:179648.CrossRefPubMedPubMedCentral Gorska-Ciebiada M, Saryusz-Wolska M, Ciebiada M, Loba J. Mild cognitive impairment and depressive symptoms in elderly patients with diabetes: prevalence, risk factors, and comorbidity. J Diabetes Res. 2014;2014:179648.CrossRefPubMedPubMedCentral
22.
Zurück zum Zitat Dejenie Habtewold T, Radie YT, Sharew NT. Prevalence of depression among type 2 diabetic outpatients in black lion general specialized hospital, Addis Ababa, Ethiopia. Depress Res Treat. 2015;2015:184902.PubMedPubMedCentral Dejenie Habtewold T, Radie YT, Sharew NT. Prevalence of depression among type 2 diabetic outpatients in black lion general specialized hospital, Addis Ababa, Ethiopia. Depress Res Treat. 2015;2015:184902.PubMedPubMedCentral
23.
Zurück zum Zitat Erkie M, Feleke Y, Desalegne F, Anbessie J, Shibre T. Magnitude, clinical and sociodemographic correlate of depression in diabetic patients, Addis Ababa, Ethiopia. Ethiop Med J. 2013;51(4):249–59.PubMed Erkie M, Feleke Y, Desalegne F, Anbessie J, Shibre T. Magnitude, clinical and sociodemographic correlate of depression in diabetic patients, Addis Ababa, Ethiopia. Ethiop Med J. 2013;51(4):249–59.PubMed
24.
Zurück zum Zitat Khan MA, Sultan SM, Nazli R, Akhtar T, Khan MA, Sher N, et al. Depression among patients with type-II diabetes mellitus. J Coll Physicians Surg Pak. 2014;24(10):770–1.PubMed Khan MA, Sultan SM, Nazli R, Akhtar T, Khan MA, Sher N, et al. Depression among patients with type-II diabetes mellitus. J Coll Physicians Surg Pak. 2014;24(10):770–1.PubMed
25.
Zurück zum Zitat Birhanu AM, Alemu FM, Ashenafie TD, Balcha SA, Dachew BA. Depression in diabetic patients attending University of Gondar Hospital Diabetic clinic, Northwest Ethiopia. Diabetes Metab Syndr Obes. 2016;9:155.PubMedPubMedCentral Birhanu AM, Alemu FM, Ashenafie TD, Balcha SA, Dachew BA. Depression in diabetic patients attending University of Gondar Hospital Diabetic clinic, Northwest Ethiopia. Diabetes Metab Syndr Obes. 2016;9:155.PubMedPubMedCentral
26.
Zurück zum Zitat Engel, GL. The need for a new medical model: a challenge for biomedicine. Science. 1977;196(4286):129–36.CrossRefPubMed Engel, GL. The need for a new medical model: a challenge for biomedicine. Science. 1977;196(4286):129–36.CrossRefPubMed
27.
Zurück zum Zitat Hatala AR. The status of the “biopsychosocial” model in health psychology: towards an integrated approach and a critique of cultural conceptions. Open J Med Psychol. 2012;1(4):51–62.CrossRef Hatala AR. The status of the “biopsychosocial” model in health psychology: towards an integrated approach and a critique of cultural conceptions. Open J Med Psychol. 2012;1(4):51–62.CrossRef
28.
Zurück zum Zitat Ghaemi SN. The rise and fall of the biopsychosocial model. Br J Psychiatry. 2009;195(1):3–4.CrossRefPubMed Ghaemi SN. The rise and fall of the biopsychosocial model. Br J Psychiatry. 2009;195(1):3–4.CrossRefPubMed
29.
Zurück zum Zitat Tavakoli HR. A closer evaluation of current methods in psychiatric assessments: a challenge for the biopsychosocial model. Psychiatry (Edgmont). 2009;6(2):25–30. Tavakoli HR. A closer evaluation of current methods in psychiatric assessments: a challenge for the biopsychosocial model. Psychiatry (Edgmont). 2009;6(2):25–30.
30.
Zurück zum Zitat Schotte CK, Van Den Bossche B, De Doncker D, Claes S, Cosyns P. A biopsychosocial model as a guide for psychoeducation and treatment of depression. Depress Anxiety. 2006;23(5):312–24.CrossRefPubMed Schotte CK, Van Den Bossche B, De Doncker D, Claes S, Cosyns P. A biopsychosocial model as a guide for psychoeducation and treatment of depression. Depress Anxiety. 2006;23(5):312–24.CrossRefPubMed
31.
Zurück zum Zitat Garcia-Toro M, Aguirre I. Biopsychosocial model in depression revisited. Med Hypotheses. 2007;68(3):683–91.CrossRefPubMed Garcia-Toro M, Aguirre I. Biopsychosocial model in depression revisited. Med Hypotheses. 2007;68(3):683–91.CrossRefPubMed
32.
Zurück zum Zitat Frankel RM, Quill TE, McDaniel SH. The biopsychosocial approach: past, present, and future. Rochester: University Rochester Press; 2003. Frankel RM, Quill TE, McDaniel SH. The biopsychosocial approach: past, present, and future. Rochester: University Rochester Press; 2003.
33.
Zurück zum Zitat Campbell LC, Clauw DJ, Keefe FJ. Persistent pain and depression: a biopsychosocial perspective. Biol Psychiatry. 2003;54(3):399–409.CrossRefPubMed Campbell LC, Clauw DJ, Keefe FJ. Persistent pain and depression: a biopsychosocial perspective. Biol Psychiatry. 2003;54(3):399–409.CrossRefPubMed
34.
Zurück zum Zitat Havelka M, Lučanin JD, Lučanin D. Biopsychosocial model–the integrated approach to health and disease. Coll Antropol. 2009;33(1):303–10.PubMed Havelka M, Lučanin JD, Lučanin D. Biopsychosocial model–the integrated approach to health and disease. Coll Antropol. 2009;33(1):303–10.PubMed
35.
Zurück zum Zitat Robbins A. Biopsychosocial aspects in understanding and treating depression in men: a clinical perspective. J Men’s Health Gend. 2006;3(1):10–8.CrossRef Robbins A. Biopsychosocial aspects in understanding and treating depression in men: a clinical perspective. J Men’s Health Gend. 2006;3(1):10–8.CrossRef
37.
Zurück zum Zitat Yu X, Tam WW, Wong PT, Lam TH, Stewart SM. The patient health questionnaire-9 for measuring depressive symptoms among the general population in Hong Kong. Compr Psychiatry. 2012;53(1):95–102.CrossRefPubMed Yu X, Tam WW, Wong PT, Lam TH, Stewart SM. The patient health questionnaire-9 for measuring depressive symptoms among the general population in Hong Kong. Compr Psychiatry. 2012;53(1):95–102.CrossRefPubMed
38.
Zurück zum Zitat Gelaye B, Williams MA, Lemma S, Deyessa N, Bahretibeb Y, Shibre T, et al. Validity of the patient health questionnaire-9 for depression screening and diagnosis in East Africa. Psychiatry Res. 2013;210(2):653–61.CrossRefPubMed Gelaye B, Williams MA, Lemma S, Deyessa N, Bahretibeb Y, Shibre T, et al. Validity of the patient health questionnaire-9 for depression screening and diagnosis in East Africa. Psychiatry Res. 2013;210(2):653–61.CrossRefPubMed
39.
Zurück zum Zitat Naranjo DM, Fisher L, Arean PA, Hessler D, Mullan J. Patients with type 2 diabetes at risk for major depressive disorder over time. Ann Fam Med. 2011;9(2):115–20.CrossRefPubMedPubMedCentral Naranjo DM, Fisher L, Arean PA, Hessler D, Mullan J. Patients with type 2 diabetes at risk for major depressive disorder over time. Ann Fam Med. 2011;9(2):115–20.CrossRefPubMedPubMedCentral
40.
Zurück zum Zitat De Groot M, Anderson R, Freedland KE, Clouse RE, Lustman PJ. Association of depression and diabetes complications: a meta-analysis. Psychosom Med. 2001;63(4):619–30.CrossRefPubMed De Groot M, Anderson R, Freedland KE, Clouse RE, Lustman PJ. Association of depression and diabetes complications: a meta-analysis. Psychosom Med. 2001;63(4):619–30.CrossRefPubMed
41.
Zurück zum Zitat Demmer RT, Gelb S, Suglia SF, Keyes KM, Aiello AE, Colombo PC, et al. Sex differences in the association between depression, anxiety, and type 2 diabetes mellitus. Psychosom Med. 2015;77(4):467–77.CrossRefPubMedPubMedCentral Demmer RT, Gelb S, Suglia SF, Keyes KM, Aiello AE, Colombo PC, et al. Sex differences in the association between depression, anxiety, and type 2 diabetes mellitus. Psychosom Med. 2015;77(4):467–77.CrossRefPubMedPubMedCentral
42.
Zurück zum Zitat Hapunda G, Abubakar A, Pouwer F, van de Vijver F. Diabetes mellitus and comorbid depression in Zambia. Diabet Med. 2015;32(6):814–8.CrossRefPubMed Hapunda G, Abubakar A, Pouwer F, van de Vijver F. Diabetes mellitus and comorbid depression in Zambia. Diabet Med. 2015;32(6):814–8.CrossRefPubMed
43.
Zurück zum Zitat Lopez-de-Andres A, Jimenez-Trujillo MI, Hernandez-Barrera V, de Miguel-Yanes JM, Mendez-Bailon M, Perez-Farinos N, et al. Trends in the prevalence of depression in hospitalized patients with type 2 diabetes in Spain: analysis of hospital discharge data from 2001 to 2011. PLoS ONE. 2015;10(2):e0117346.CrossRefPubMedPubMedCentral Lopez-de-Andres A, Jimenez-Trujillo MI, Hernandez-Barrera V, de Miguel-Yanes JM, Mendez-Bailon M, Perez-Farinos N, et al. Trends in the prevalence of depression in hospitalized patients with type 2 diabetes in Spain: analysis of hospital discharge data from 2001 to 2011. PLoS ONE. 2015;10(2):e0117346.CrossRefPubMedPubMedCentral
44.
Zurück zum Zitat Milanovic SM, Erjavec K, Poljicanin T, Vrabec B, Brecic P. Prevalence of depression symptoms and associated socio-demographic factors in primary health care patients. Psychiatr Danub. 2015;27(1):31–7.PubMed Milanovic SM, Erjavec K, Poljicanin T, Vrabec B, Brecic P. Prevalence of depression symptoms and associated socio-demographic factors in primary health care patients. Psychiatr Danub. 2015;27(1):31–7.PubMed
45.
Zurück zum Zitat Mir K, Mir K, Malik I, Shehzadi A. Prevalence of co-morbid depression in diabetic population. J Ayub Med Coll Abbottabad. 2015;27(1):99–101.PubMed Mir K, Mir K, Malik I, Shehzadi A. Prevalence of co-morbid depression in diabetic population. J Ayub Med Coll Abbottabad. 2015;27(1):99–101.PubMed
46.
Zurück zum Zitat Berge LI, Riise T, Tell GS, Iversen MM, Ostbye T, Lund A, et al. Depression in persons with diabetes by age and antidiabetic treatment: a cross-sectional analysis with data from the Hordaland Health Study. PLoS ONE. 2015;10(5):e0127161.CrossRefPubMedPubMedCentral Berge LI, Riise T, Tell GS, Iversen MM, Ostbye T, Lund A, et al. Depression in persons with diabetes by age and antidiabetic treatment: a cross-sectional analysis with data from the Hordaland Health Study. PLoS ONE. 2015;10(5):e0127161.CrossRefPubMedPubMedCentral
47.
Zurück zum Zitat Park CY, Kim SY, Gil JW, Park MH, Park JH, Kim Y. Depression among Korean adults with type 2 diabetes mellitus: Ansan-Community-Based Epidemiological Study. Osong Public Health Res Perspect. 2015;6(4):224–32.CrossRefPubMedPubMedCentral Park CY, Kim SY, Gil JW, Park MH, Park JH, Kim Y. Depression among Korean adults with type 2 diabetes mellitus: Ansan-Community-Based Epidemiological Study. Osong Public Health Res Perspect. 2015;6(4):224–32.CrossRefPubMedPubMedCentral
48.
Zurück zum Zitat Kyung Lee H, Hee Lee S. Depression, diabetes, and healthcare utilization: results from the Korean Longitudinal Study of Aging (KLoSA). Iran J Public Health. 2014;43(1):6–15.PubMedPubMedCentral Kyung Lee H, Hee Lee S. Depression, diabetes, and healthcare utilization: results from the Korean Longitudinal Study of Aging (KLoSA). Iran J Public Health. 2014;43(1):6–15.PubMedPubMedCentral
49.
Zurück zum Zitat Davis TM, Hunt K, Bruce DG, Starkstein S, Skinner T, McAullay D, et al. Prevalence of depression and its associations with cardio-metabolic control in Aboriginal and Anglo-Celt patients with type 2 diabetes: the Fremantle Diabetes Study Phase II. Diabetes Res Clin Pract. 2015;107(3):384–91.CrossRefPubMed Davis TM, Hunt K, Bruce DG, Starkstein S, Skinner T, McAullay D, et al. Prevalence of depression and its associations with cardio-metabolic control in Aboriginal and Anglo-Celt patients with type 2 diabetes: the Fremantle Diabetes Study Phase II. Diabetes Res Clin Pract. 2015;107(3):384–91.CrossRefPubMed
50.
Zurück zum Zitat De la Roca-Chiapas JM, Hernandez-Gonzalez M, Candelario M, Villafana Mde L, Hernandez E, Solorio S, et al. Association between depression and higher glucose levels in middle-aged Mexican patients with diabetes. Rev Invest Clin. 2013;65(3):209–13.PubMed De la Roca-Chiapas JM, Hernandez-Gonzalez M, Candelario M, Villafana Mde L, Hernandez E, Solorio S, et al. Association between depression and higher glucose levels in middle-aged Mexican patients with diabetes. Rev Invest Clin. 2013;65(3):209–13.PubMed
51.
Zurück zum Zitat Foran E, Hannigan A, Glynn L. Prevalence of depression in patients with type 2 diabetes mellitus in Irish primary care and the impact of depression on the control of diabetes. Ir J Med Sci. 2015;184(2):319–22.CrossRefPubMed Foran E, Hannigan A, Glynn L. Prevalence of depression in patients with type 2 diabetes mellitus in Irish primary care and the impact of depression on the control of diabetes. Ir J Med Sci. 2015;184(2):319–22.CrossRefPubMed
52.
Zurück zum Zitat Sweileh WM, Abu-Hadeed HM, Al-Jabi SW, Zyoud SH. Prevalence of depression among people with type 2 diabetes mellitus: a cross sectional study in Palestine. BMC Public Health. 2014;14:163.CrossRefPubMedPubMedCentral Sweileh WM, Abu-Hadeed HM, Al-Jabi SW, Zyoud SH. Prevalence of depression among people with type 2 diabetes mellitus: a cross sectional study in Palestine. BMC Public Health. 2014;14:163.CrossRefPubMedPubMedCentral
53.
Zurück zum Zitat Siddiqui S. Depression in type 2 diabetes mellitus—a brief review. Diabetes Metab Syndr. 2014;8(1):62–5.CrossRefPubMed Siddiqui S. Depression in type 2 diabetes mellitus—a brief review. Diabetes Metab Syndr. 2014;8(1):62–5.CrossRefPubMed
54.
Zurück zum Zitat Frederick FT, Maharajh HD. Prevalence of depression in type 2 diabetic patients in Trinidad and Tobago. West Indian Med J. 2013;62(7):628–31.PubMed Frederick FT, Maharajh HD. Prevalence of depression in type 2 diabetic patients in Trinidad and Tobago. West Indian Med J. 2013;62(7):628–31.PubMed
55.
Zurück zum Zitat Ryerson B, Tierney EF, Thompson TJ, Engelgau MM, Wang J, Gregg EW, et al. Excess physical limitations among adults with diabetes in the U.S. population, 1997–1999. Diabetes Care. 2003;26(1):206–10.CrossRefPubMed Ryerson B, Tierney EF, Thompson TJ, Engelgau MM, Wang J, Gregg EW, et al. Excess physical limitations among adults with diabetes in the U.S. population, 1997–1999. Diabetes Care. 2003;26(1):206–10.CrossRefPubMed
56.
Zurück zum Zitat Zahid N, Asghar S, Claussen B, Hussain A. Depression and diabetes in a rural community in Pakistan. Diabetes Res Clin Pract. 2008;79(1):124–7.CrossRefPubMed Zahid N, Asghar S, Claussen B, Hussain A. Depression and diabetes in a rural community in Pakistan. Diabetes Res Clin Pract. 2008;79(1):124–7.CrossRefPubMed
57.
Zurück zum Zitat Musselman DL, Betan E, Larsen H, Phillips LS. Relationship of depression to diabetes types 1 and 2: epidemiology, biology, and treatment. Biol Psychiatry. 2003;54(3):317–29.CrossRefPubMed Musselman DL, Betan E, Larsen H, Phillips LS. Relationship of depression to diabetes types 1 and 2: epidemiology, biology, and treatment. Biol Psychiatry. 2003;54(3):317–29.CrossRefPubMed
58.
Zurück zum Zitat Pouwer F, Geelhoed-Duijvestijn P, Tack C, Bazelmans E, Beekman A, Heine R, et al. Prevalence of comorbid depression is high in out-patients with Type 1 or Type 2 diabetes mellitus. Results from three out-patient clinics in the Netherlands. Diabet Med. 2010;27(2):217–24.CrossRefPubMed Pouwer F, Geelhoed-Duijvestijn P, Tack C, Bazelmans E, Beekman A, Heine R, et al. Prevalence of comorbid depression is high in out-patients with Type 1 or Type 2 diabetes mellitus. Results from three out-patient clinics in the Netherlands. Diabet Med. 2010;27(2):217–24.CrossRefPubMed
59.
Zurück zum Zitat Tapash R, Lloyd CE, Parvin M, Mohiuddin KGB, Rahman M. Prevalence of co-morbid depression in out-patients with type 2 diabetes in Bangladesh. BMC Psychiatry. 2012;12:123.CrossRef Tapash R, Lloyd CE, Parvin M, Mohiuddin KGB, Rahman M. Prevalence of co-morbid depression in out-patients with type 2 diabetes in Bangladesh. BMC Psychiatry. 2012;12:123.CrossRef
60.
Zurück zum Zitat Guruprasad K, Niranjan M, Ashwin S. A study of association of depressive symptoms among the type 2 diabetic outpatients presenting to a tertiary care hospital. Indian J Psychol Med. 2012;34(1):30.CrossRefPubMedPubMedCentral Guruprasad K, Niranjan M, Ashwin S. A study of association of depressive symptoms among the type 2 diabetic outpatients presenting to a tertiary care hospital. Indian J Psychol Med. 2012;34(1):30.CrossRefPubMedPubMedCentral
61.
Zurück zum Zitat Ell K, Katon W, Cabassa LJ, Xie B, Lee PJ, Kapetanovic S, et al. Depression and diabetes among low-income Hispanics: design elements of a socioculturally adapted collaborative care model randomized controlled trial. Int J Psychiatry Med. 2009;39(2):113–32.CrossRefPubMedPubMedCentral Ell K, Katon W, Cabassa LJ, Xie B, Lee PJ, Kapetanovic S, et al. Depression and diabetes among low-income Hispanics: design elements of a socioculturally adapted collaborative care model randomized controlled trial. Int J Psychiatry Med. 2009;39(2):113–32.CrossRefPubMedPubMedCentral
62.
Zurück zum Zitat de Groot M, Doyle T, Averyt J, Risaliti C, Shubroo J. Depressive symptoms and type 2 diabetes mellitus in rural appalachia: an 18-month follow-up study. Int J Psychiatry Med. 2015;48(4):263–77.CrossRefPubMedPubMedCentral de Groot M, Doyle T, Averyt J, Risaliti C, Shubroo J. Depressive symptoms and type 2 diabetes mellitus in rural appalachia: an 18-month follow-up study. Int J Psychiatry Med. 2015;48(4):263–77.CrossRefPubMedPubMedCentral
63.
Zurück zum Zitat Clyde M, Smith KJ, Gariepy G, Schmitz N. The association between smoking and depression in a Canadian community-based sample with type 2 diabetes. Can J Diabetes. 2013;37(3):150–5.CrossRefPubMed Clyde M, Smith KJ, Gariepy G, Schmitz N. The association between smoking and depression in a Canadian community-based sample with type 2 diabetes. Can J Diabetes. 2013;37(3):150–5.CrossRefPubMed
64.
Zurück zum Zitat Hermanns N, Kulzer B. Diabetes and depression-a burdensome co-morbidity. Eur Endocrinol. 2008;4(2):S19–22.CrossRef Hermanns N, Kulzer B. Diabetes and depression-a burdensome co-morbidity. Eur Endocrinol. 2008;4(2):S19–22.CrossRef
65.
Zurück zum Zitat Gilmer TP, Walker C, Johnson ED, Philis-Tsimikas A, Unutzer J. Improving treatment of depression among Latinos with diabetes using project Dulce and IMPACT. Diabetes Care. 2008;31(7):1324–6.CrossRefPubMedPubMedCentral Gilmer TP, Walker C, Johnson ED, Philis-Tsimikas A, Unutzer J. Improving treatment of depression among Latinos with diabetes using project Dulce and IMPACT. Diabetes Care. 2008;31(7):1324–6.CrossRefPubMedPubMedCentral
66.
Zurück zum Zitat Camara A, Balde NM, Enoru S, Bangoura JS, Sobngwi E, Bonnet F. Prevalence of anxiety and depression among diabetic African patients in Guinea: association with HbA1c levels. Diabetes Metab. 2015;41(1):62–8.CrossRefPubMed Camara A, Balde NM, Enoru S, Bangoura JS, Sobngwi E, Bonnet F. Prevalence of anxiety and depression among diabetic African patients in Guinea: association with HbA1c levels. Diabetes Metab. 2015;41(1):62–8.CrossRefPubMed
67.
Zurück zum Zitat Kiani F, Hesabi N. The relationship between the religious beliefs of the diabetic patients and depression in a diabetes clinic in Iran. J Relig Health. 2016;55(227):1–6. Kiani F, Hesabi N. The relationship between the religious beliefs of the diabetic patients and depression in a diabetes clinic in Iran. J Relig Health. 2016;55(227):1–6.
68.
Zurück zum Zitat Agbir T, Audu M, Adebowale T, Goar S. Depression among medical outpatients with diabetes: a cross-sectional study at Jos University Teaching Hospital, Jos, Nigeria. Ann Afr Med. 2010;9(1):5–10.CrossRefPubMed Agbir T, Audu M, Adebowale T, Goar S. Depression among medical outpatients with diabetes: a cross-sectional study at Jos University Teaching Hospital, Jos, Nigeria. Ann Afr Med. 2010;9(1):5–10.CrossRefPubMed
69.
Zurück zum Zitat Egede LE, Ellis C. The effects of depression on diabetes knowledge, diabetes self-management, and perceived control in indigent patients with type 2 diabetes. Diabetes Technol Ther. 2008;10(3):213–9.CrossRefPubMed Egede LE, Ellis C. The effects of depression on diabetes knowledge, diabetes self-management, and perceived control in indigent patients with type 2 diabetes. Diabetes Technol Ther. 2008;10(3):213–9.CrossRefPubMed
70.
Zurück zum Zitat Raval A, Dhanaraj E, Bhansali A, Grover S, Tiwari P. Prevalence and determinants of depression in type 2 diabetes patients in a tertiary care centre. Indian J Med Res. 2010;132(2):195.PubMed Raval A, Dhanaraj E, Bhansali A, Grover S, Tiwari P. Prevalence and determinants of depression in type 2 diabetes patients in a tertiary care centre. Indian J Med Res. 2010;132(2):195.PubMed
71.
Zurück zum Zitat Taylor JMG, Yu M. Bias and efficiency loss due to categorizing an explanatory variable. J Multivar Anal. 2002;83(1):248–63.CrossRef Taylor JMG, Yu M. Bias and efficiency loss due to categorizing an explanatory variable. J Multivar Anal. 2002;83(1):248–63.CrossRef
72.
Zurück zum Zitat Bennette C, Vickers A. Against quantiles: categorization of continuous variables in epidemiologic research, and its discontents. BMC Med Res Methodol. 2012;12:21.CrossRefPubMedPubMedCentral Bennette C, Vickers A. Against quantiles: categorization of continuous variables in epidemiologic research, and its discontents. BMC Med Res Methodol. 2012;12:21.CrossRefPubMedPubMedCentral
73.
Zurück zum Zitat Salazar LF, Crosby RA, DiClemente RJ. Research methods in health promotion. Hoboken: Wiley; 2015. Salazar LF, Crosby RA, DiClemente RJ. Research methods in health promotion. Hoboken: Wiley; 2015.
74.
Zurück zum Zitat Naggara O, Raymond J, Guilbert F, Roy D, Weill A, Altman DG. Analysis by categorizing or dichotomizing continuous variables is inadvisable: an example from the natural history of unruptured aneurysms. AJNR Am J Neuroradiol. 2011;32(3):437–40.CrossRefPubMed Naggara O, Raymond J, Guilbert F, Roy D, Weill A, Altman DG. Analysis by categorizing or dichotomizing continuous variables is inadvisable: an example from the natural history of unruptured aneurysms. AJNR Am J Neuroradiol. 2011;32(3):437–40.CrossRefPubMed
75.
Zurück zum Zitat Weinmann S, Koesters M. Mental health service provision in low and middle-income countries: recent developments. Curr Opin Psychiatry. 2016;29(4):270–5.CrossRefPubMed Weinmann S, Koesters M. Mental health service provision in low and middle-income countries: recent developments. Curr Opin Psychiatry. 2016;29(4):270–5.CrossRefPubMed
77.
Zurück zum Zitat Lloyd CE, Sartorius N, Cimino LC, Alvarez A, Guinzbourg de Braude M, Rabbani G, et al. The INTERPRET-DD study of diabetes and depression: a protocol. Diabet Med. 2015;32(7):925–34.CrossRefPubMed Lloyd CE, Sartorius N, Cimino LC, Alvarez A, Guinzbourg de Braude M, Rabbani G, et al. The INTERPRET-DD study of diabetes and depression: a protocol. Diabet Med. 2015;32(7):925–34.CrossRefPubMed
Metadaten
Titel
Comorbidity of depression and diabetes: an application of biopsychosocial model
verfasst von
Tesfa Dejenie Habtewold
Md. Atiqul Islam
Yosef Tsige Radie
Balewgizie Sileshi Tegegne
Publikationsdatum
01.12.2016
Verlag
BioMed Central
Erschienen in
International Journal of Mental Health Systems / Ausgabe 1/2016
Elektronische ISSN: 1752-4458
DOI
https://doi.org/10.1186/s13033-016-0106-2

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