Erschienen in:
16.10.2021 | Meta- Analysis
Polycystic ovary syndrome is an independent risk factor for hypertensive disorders of pregnancy: A systematic review, meta-analysis, and meta-regression
verfasst von:
Haixia Pan, Peiyi Xian, Daopeng Yang, Chunren Zhang, Huizhen Tang, Xiaoying He, Han Lin, Xiaohui Wen, Hongxia Ma, Maohua Lai
Erschienen in:
Endocrine
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Ausgabe 3/2021
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Abstract
Purpose
The risk of hypertensive disorders of pregnancy (HDP) in women with polycystic ovary syndrome (PCOS) is inconsistent in some studies. The aim of this meta-analysis was to examine the evidence regarding the strength of the association between PCOS and HDP.
Methods
PubMed, Web of Science, Embase, and the Cochrane Library were systematically searched to identify observational studies investigating HDP in patients with PCOS. The primary outcome was the pooled odds ratio (OR) of HDP, including pregnancy-induced hypertension (PIH) and pre-eclampsia (PE), in women with PCOS compared with the non-PCOS population.
Results
A total of 30 studies were eligible for meta-analysis. PCOS was associated with a higher risk of HDP (OR 2.02, 95CI% 1.83–2.22), including PIH (OR 1.94, 95CI% 1.70–2.21), and PE (OR 2.07, 95CI% 1.91–2.24). The association remained significant after adjusting for age, body mass index (BMI), and nulliparity (HDP: OR 1.48, 95CI% 1.48–1.60; PIH: OR 1.42, 95%CI 1.29–1.57; PE: OR 2.07, and 95%CI 1.91–2.24). The increased risk of HDP for the PCOS group remained significant in subgroups of BMI, Age, singleton pregnancy, multiple pregnancy, gestational diabetes mellitus (GDM), hyperandrogenism, and nulliparity, while the finding was not observed in subgroups of nonhyperandrogenic and non-GDM. In the meta-regression, BMI contributed significantly to the heterogeneity in the prevalence of HDP.
Conclusions
PCOS is independently associated with a significantly increased risk of HDP. To prevent HDP during pregnancy, our findings highlight the importance of establishing supervision guidelines for PCOS patients, especially in the population with hyperandrogenism and GDM.