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Erschienen in: Reproductive Biology and Endocrinology 1/2016

Open Access 01.12.2016 | Research

Assisted reproductive technology pregnancy complications are significantly associated with endometriosis severity before conception: a retrospective cohort study

verfasst von: Tatsuya Fujii, Osamu Wada-Hiraike, Takeshi Nagamatsu, Miyuki Harada, Tetsuya Hirata, Kaori Koga, Tomoyuki Fujii, Yutaka Osuga

Erschienen in: Reproductive Biology and Endocrinology | Ausgabe 1/2016

Abstract

Background

Endometriosis has been shown to be associated with second- to third-trimester pregnancy complications such as preterm birth and placenta previa, but the evidence is inconsistent. We hypothesized that endometriosis severity might affect these inconsistent results. Therefore we aimed to conduct a retrospective cohort study to elucidate whether endometriosis severity is associated with the incidence rates of adverse pregnancy outcomes.

Methods

The patients who achieved singleton pregnancy by assisted reproductive technology (ART) in our facility between March 2000 and December 2014 (N = 631) were included in this analysis. Among them, 92 women demonstrated surgically proven endometriosis, and 512 women were shown to not have endometriosis as a complication. Among the 92 cases of endometriosis, 10 were classified as revised American Society for Reproductive Medicine (rASRM) stage I and II, 31 cases were rASRM stage III, and 43 cases were rASRM stage IV; in 8 cases, the rASRM stage was unavailable. Logistic regression analysis was performed to calculate odds ratios (OR) and 95 % confidence interval (CI) for the rates of preterm birth, placenta previa, and small for gestational age. OR were adjusted by age, parity and the number of transferred embryos.

Results

First we confirmed the frequency of preterm birth and placenta previa were significantly increased in women with endometriosis (preterm birth OR, 2.08; 95 % CI, 1.07–3.89, placenta previa OR, 15.1; 95 % CI, 4.40–61.7), while the frequency of small for gestational age was not. Moreover, we found the frequencies of preterm birth and placenta previa were significantly increased in women with rASRM stage IV endometriosis compared to other two groups: women with rASRM stage I-III endometriosis (preterm birth OR, 7.40; 95 % CI, 1.83–50.3; placenta previa OR, 11.0; 95 % CI, 1.75–216.5) and women without endometriosis (preterm birth adjusted OR, 4.11; 95 % CI, 1.88–8.55; placenta previa adjusted OR, 39.8; 95 % CI, 10.1–189.1). There were no significant difference between women with rASRM I-III endometriosis and women without endometriosis.

Conclusions

We found that the frequencies of preterm birth and placenta previa were significantly increased in women with endometriosis, and the severity of endometriosis might have an adverse impact on ART pregnancy.
Abkürzungen
AOR
Adjusted odds ratio
ART
Assisted reproductive technology
CI
Confidence interval
PR
Progesterone receptor
rASRM
Revised American Society for Reproductive Medicine
SGA
Small for gestational age
Th
T helper

Background

Endometriosis is defined as an abnormal development of endometrial tissue outside the uterus. This condition causes chronic inflammation in the pelvis of reproductive-aged women. Estrogen is associated with the pathogenesis of endometriosis because the symptoms related to endometriosis resolve soon after the cessation of menstruation. The chronic inflammation results in the generation of ovarian endometrioma and the formation of adhesions in the reproductive organs; thus, it is well known that this disease is associated with infertility [1, 2]. In addition, the T helper (Th)1/Th2 balance has been established to be disrupted in patients with endometriosis [3]. Moreover, endometriosis might affect the expression patterns of progesterone receptors (PR) A and PR B [4].
Recently, endometriosis has been shown to be associated with second- to third-trimester pregnancy complications, such as preterm birth, preeclampsia, small for gestational age (SGA) and placenta previa [36]. However, several investigators have reported that the association between endometriosis and pregnancy complications is questionable [79], and the association remains under debate [10, 11]. Some reports have suggested that not endometriosis itself but ovarian endometrioma and rectovaginal endometriosis might be associated with adverse pregnancy outcomes. A retrospective cohort study suggested that ovarian endometrioma was associated with preterm birth, but endometriosis without ovarian endometrioma was not associated with preterm birth in assisted reproductive technology (ART) pregnancy [12]. An association between placenta previa and rectovaginal endometriosis has been previously reported [7]. However multivariate analysis was not performed in this study, and evidence is limited. From these observations, it is still difficult to conclude what types of endometriosis increases the risk for pregnancy complications.
In general, minimal and mild endometriosis correspond to peritoneal disease, while moderate endometriosis corresponds to one ovarian endometrioma > 3 cm, and severe endometriosis corresponds to bilateral endometriomas and/or complete pouch of Douglas obliteration, according to the revised American Society for Reproductive Medicine (rASRM) scoring system, which is widely used to evaluate and stage endometriosis severity [1]. To take into account the association between ovarian endometrioma or rectovaginal endometriosis and the increased rates of preterm birth and placenta previa, we hypothesized that rASRM stage might affect the incidence rates of these pregnancy complications. Therefore, the aim of this study was to evaluate the association between endometriosis and pregnancy complications as well as to investigate the influence of endometriosis severity on pregnancy complication outcomes using the rASRM scoring system.

Methods

Sample collection

The demographic data of each case were recorded in a medical record of our hospital. These data included the patient’s age, parity, past medical history including surgical records, suspected causes of infertility, the number of transferred embryos and pregnancy outcomes. Sample collection was performed by extracting data from these records. According to the database, 631 singleton babies were born as a result of ART performed in our hospital between March 2000 and December 2014.

Diagnosis and surgical treatment of endometriosis

Laparoscopy is the most reliable procedure for diagnosing and classifying endometriosis [1]. Therefore, current data were based on laparoscopic findings to accurately evaluate the risks of pregnancy with endometriosis. In each case, therapeutic procedures, such as adhesiotomy, coagulation, and cystectomy, were performed by trained personnel at our hospital to treat the detected endometriosis.
The women who had laparoscopically diagnosed endometriosis were categorized as “endometriosis diagnosed by laparoscopy” (n = 92). The women who were suspected to have endometriosis by transvaginal ultrasound or medical history but did not undergo laparoscopy were categorized as having “suspected endometriosis” and were excluded from this study (n = 20). The other women who were not suspected to have endometriosis by transvaginal ultrasound or in whom the presence of endometriosis was denied by laparoscopy were categorized as “denied presence of endometriosis” (n = 512). The women classified as “endometriosis diagnosed by laparoscopy” and “denied presence of endometriosis” were included in this study. Seven women were excluded because of complications before pregnancy; four suffered endometrial cancer, one was diagnosed with cervical cancer in early pregnancy, and two were recovering from conization. We used the rASRM scoring system to evaluate the severity of endometriosis because this is a widely accepted scoring system [1]. Of the 92 cases of laparoscopically diagnosed endometriosis, 10 cases were rASRM stage I and II, 31 were rASRM stage III, and 43 were rASRM stage IV; in 8 cases, the rASRM stage was unavailable. Sample collection criteria was summarized in Fig. 1.

Complication outcomes during pregnancy

We analyzed following adverse pregnancy outcomes: preterm birth, placenta previa, and SGA. The definitions used in this study for the diagnosis of these complications was as follows. Preterm birth was defined as delivery before 37 complete weeks of gestation. Placenta previa was defined as the condition in which the placenta at least partially covered the internal ostium. SGA defined as an infant weight less than the 10th percentile for the gestational age.

Statistical analysis

All statistical analyses were performed using JMP PRO 11 software (SAS Institute Inc., Cary, NC, USA). Fisher’s exact test was used to calculate p values for the comparison of maternal characteristics with or without endometriosis. Logistic regression analysis was used to calculate the adjusted odds ratios (AORs) and 95 % confidence intervals (CIs) in the analysis of adverse pregnancy outcomes. Odds ratios were adjusted by age, parity and the number of transferred embryos.

Results

Characteristics of the patients included in this study

The preconceptional characteristics of the patients included in this study are summarized in Table 1. There were no significant differences in age, previous parity or the number of embryos transferred between the women with or without endometriosis.
Table 1
Characteristics of women with ART pregnancy
 
ART with endometriosis
ART without endometriosis
P value
N
92
512
 
Age (year, mean)
34.7
35.4
0.078
Previous parity
  
0.29
0
78 (84.8 %)
396 (77.6 %)
 
1
14 (15.2 %)
113 (22.2 %)
 
2
0
1 (0.2 %)
 
No. of ET for conception
  
0.788
1
55 (59.8 %)
292 (57.0 %)
 
2
28 (30.4 %)
151 (29.5 %)
 
3
9 (9.8 %)
68 (13.3 %)
 
4
0
1 (0.2 %)
 
Note: ART assisted reproductive technology; ET embryos transferred

Preterm birth and placenta previa were increased in women with endometriosis

The risks of preterm birth, placenta previa, and SGA in ART pregnancy with or without endometriosis are shown in Table 2. The risks of preterm birth and placenta previa were significantly increased in the pregnant women with endometriosis (preterm birth AOR, 2.08; 95 % CI, 1.07–3.89, placenta previa AOR, 15.1; 95 % CI, 4.40–61.7). No significant difference was found in the risk of SGA.
Table 2
Complications during pregnancy in women with or without endometriosis
 
ART with endometriosis
ART without endometriosis
Odds ratio (95 % Cl)a
P value
Preterm birth
15 (16.5 %)
43 (8.5 %)
2.08 (1.07–3.89)
0.032
Placenta previa
8 (9.1 %)
4 (0.8 %)
15.1 (4.40–61.7)
< 0.001
SGA
11 (14.1 %)
52 (10.3 %)
1.43 (0.68–2.81)
0.332
SGA small for gestational age, CI confidence interval
aAdjusted by age, parity, and the number of transferred embryos

Preterm birth and placenta previa were increased in women with rASRM stage IV but not stage I-III endometriosis

The risks of adverse pregnancy outcomes were compared among the following three groups: the women with rASRM stage I–III endometriosis, the women with rASRM stage IV endometriosis and the women without endometriosis. The risks of preterm birth and placenta previa were significantly increased in the women with rASRM stage IV endometriosis compared to the women with rASRM stage I-III endometriosis (preterm birth AOR, 7.40; 95 % CI, 1.83–50.3; placenta previa AOR, 11.0; 95 % CI, 1.75–216.5) and to the women without endometriosis (preterm birth AOR, 4.11; 95 % CI, 1.88–8.55; placenta previa AOR, 39.8; 95 % CI, 10.1–189.1). However, the risks of these adverse pregnancy outcomes were not increased in the women with rASRM stage I-III endometriosis compared to the women without endometriosis. No significant differences were found in the risk of SGA between any two groups (Table 3).
Table 3
Comparison of complications classified by endometriosis severity
 
rASRM stage I – III
Odds ratio (95 % Cl)a
rASRM stage IV
Odds ratio (95 % Cl)a
Odds ratio (95 % Cl)b
Preterm birth
2 (4.9 %)
0.55 (0.09–1.90)
12 (27.9 %)
4.11 (1.88–8.55)***
7.40 (1.83–50.3)***
Placenta Previa
1 (2.4 %)
3.61 (0.18–26.3)
7 (17.1 %)
39.8 (10.1–189.1)***
11.0 (1.75–216.5)***
SGA
4 (10.3 %)
0.99 (0.29–2.61)
7 (20.6 %)
2.30 (0.88–5.37)
2.32 (0.63–9.70)
rASRM revised American Society for Reproductive Medicine
***p < 0.05
aAdjusted odds ratio toward ART without endometriosis
bAdjusted odds ratio of rASRM stage IV toward rASRM stage I-III

Discussion

From this study, we found that ART pregnancy complicated with endometriosis carries a high risk of preterm birth and placenta previa, especially in women with rASRM stage IV endometriosis. The incidence rates of preterm birth and placenta previa in rASRM stage IV (27.9 and 17.1 %, respectively) were surprisingly high compared to the general incidence rates reported in Japan (5–6 and 0.5–0.7 %, respectively) [12, 13]. These data suggest that there is a strong association between severe endometriosis and these pregnancy complications. To our knowledge, this is the first report to suggest the correlation of endometriosis severity and adverse outcomes in the second and third trimester of pregnancy.
This study was only included ART pregnancies to avoid the influence of conception methods. ART pregnancy is known to carry a high risk of adverse pregnancy outcomes, such as preterm birth and placenta previa, compared with natural conception [14, 15]; however, the underlying mechanism of the increased risk for adverse outcomes in ART pregnancy remains unclear. One report suggests that not only the ART procedure itself but also underlying causes of infertility might be associated with adverse pregnancy outcomes in ART pregnancy [16]. According to this point of view, we could also conclude that endometriosis, one of the most prevalent diseases causing infertility in women, might be a crucial factor of increased adverse outcomes in ART pregnancy.
On the other hand, rASRM stage I-III endometriosis followed by therapeutic laparoscopic procedures might not be associated with second- and third- trimester pregnancy complications. While the sample size of rASRM stage I-III endometriosis in this study was insufficient to completely deny the association between minimal to moderate endometriosis and pregnancy complications, at least strong associations were not recognized in this study. These results seemed to be inconsistent with those of past studies, which suggested an association of endometrioma with preterm birth [12]; however, we have to consider that no endometriomas were present at the time of conception in most cases included in this study because of therapeutic procedures performed for endometriosis. In that context, our results are consistent with those of past studies.
These results are also interesting in terms of the mechanisms underlying the increased risks of pregnancy complications in women with endometriosis. In most cases in this study, ovarian endometriomas were almost completely removed by laparoscopic surgery, and apparent recurrences were not observed. However, strong adhesions mainly recognized in rASRM stage IV cases were not completely removed. We speculate that these remaining adhesions and inflammation in the rectovaginal region might be the main cause of the increased risks of preterm birth and placenta previa, as previously suggested [7].
This study also had some limitations. Adenomyosis is a disease characterized by the presence of endometrial tissue deep within the uterine myometrium [17], and an association of adenomyosis with preterm birth has been previously reported [16, 17]. Therefore, adenomyosis might have influenced the increased incidence rate of preterm birth in this study. On the other hand, to the best of our knowledge, no reports have suggested an association between adenomyosis and placenta previa. Further research is needed to elucidate the influence of adenomyosis on the increased risk of preterm birth in women with endometriosis.

Conclusion

We found that ART pregnancies complicated with endometriosis, especially laparoscopically diagnosed severe endometriosis, and carried a high risk for preterm birth and placenta previa. These findings are clinically relevant to obstetricians for distinguishing high- and low-risk pregnancies.

Acknowledgements

The authors would like to thank American Journal Experts (www.​aje.​com) for the English language review.

Funding

This study was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science and Culture (Grant no. 24592505), Ministry of Health, Labour and Welfare, Japan Agency for Medical Research and Development, and The Japanese Foundation for Research and Promotion of Endoscopy Grant.

Availability of data and materials

The datasets during and/or analyzed during the current study available from the corresponding author on reasonable request.

Authors’ contributions

TF carried out all of the sample collection and analysis of data. OW-H has been involved in acquisition of data, drafting the manuscript, and revising it critically for important intellectual content. TN, MH, TH and KK have made substantial contributions to conception and design, analysis and interpretation of data. TF and YO have given final approval of the version to be submitted. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.
Not applicable.
This study is approved by ethics Institutional Review Board.
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.
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Metadaten
Titel
Assisted reproductive technology pregnancy complications are significantly associated with endometriosis severity before conception: a retrospective cohort study
verfasst von
Tatsuya Fujii
Osamu Wada-Hiraike
Takeshi Nagamatsu
Miyuki Harada
Tetsuya Hirata
Kaori Koga
Tomoyuki Fujii
Yutaka Osuga
Publikationsdatum
01.12.2016
Verlag
BioMed Central
Erschienen in
Reproductive Biology and Endocrinology / Ausgabe 1/2016
Elektronische ISSN: 1477-7827
DOI
https://doi.org/10.1186/s12958-016-0209-2

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