Chen Xinxia, Gissler Mika, Lavebratt Catharina
School of Nursing and Rehabilitation, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Hum Reprod Open. 2023 Dec 4;2023(4):hoad048. doi: 10.1093/hropen/hoad048. eCollection 2023.
Is polycystic ovary syndrome (PCOS) associated with higher risks of extreme birth size and/or preterm birth in mothers with different hypertension types?
PCOS was associated with additional risks of preterm birth in mothers with chronic hypertension and in singleton pregnancies of mothers with pre-eclampsia, and with higher risks of offspring born large for gestational age (LGA) in mothers with gestational hypertension.
Women with PCOS are more likely to develop gestational hypertension, pre-eclampsia, and chronic hypertension. Although adverse birth outcomes have been frequently reported in mothers with PCOS, such associations in the setting of a hypertensive disorder remain unknown.
This is a population-based cohort study including all live births 2004-2014 in Finland (n = 652 732). To ensure diagnosis specificity, mothers with diagnoses that could cause signs and symptoms resembling PCOS were excluded.
PARTICIPANTS/MATERIALS SETTING METHODS: Maternal diagnoses of PCOS, gestational hypertension, chronic hypertension, and pre-eclampsia were identified from the Finnish national registries. Generalized estimating equation and multivariable logistic regression were used to assess the adjusted odds ratio (aOR) and 95% CIs of preterm birth, very preterm birth, and offspring being small for gestational age (SGA) or LGA in hypertensive mothers with or without PCOS, using normotensive mothers without PCOS as reference.
Of 43 902 (6.7%) mothers with hypertensive disorders, 1709 (3.9%) had PCOS. Significant interactions were detected for PCOS with hypertension on preterm birth, very preterm birth, offspring born SGA and LGA ( =504.1, < 0.001; =124.2, < 0.001; =99.5, < 0.001; =2.7, = 0.012, respectively). Using mothers with no hypertensive disorder and no PCOS as reference, the risks of preterm and very preterm birth were overrepresented in non-PCOS mothers with chronic hypertension or pre-eclampsia. PCOS was associated with higher risks of preterm birth (aOR 4.02, 3.14-5.15 vs aOR 2.51, 2.32-2.71) in mothers with chronic hypertension, with significant interaction between the exposures (=32.7, < 0.001). PCOS was also associated with a higher risk of preterm birth in singleton pregnancies of mothers with pre-eclampsia (aOR 7.33, 5.92-9.06 vs aOR 5.72, 5.43-6.03; =50.0, < 0.001). Furthermore, the associations of PCOS comorbid with chronic hypertension or pre-eclampsia was detected also for spontaneous births. Moreover, the risk of offspring LGA was higher in mothers with PCOS and gestational hypertension although lower in those with gestational hypertension alone (aOR 2.04, 1.48-2.80 vs aOR 0.80, 0.72-0.89; =9.7, = 0.002), whereas for offspring SGA, the risks were comparable between hypertensive mothers with and those without PCOS.
Information on medication treatment, gestational weeks of onset for pre-eclampsia and gestational hypertension, weight gain during pregnancy, and PCOS phenotypes were not available. All diagnoses were retrieved from registries, representing only those seeking medical care for their symptoms. The ICD-9 codes used to identify PCOS before year 1996 are known to underestimate the prevalence of PCOS, while the inclusion of anovulatory infertility as PCOS might introduce an overrepresentation bias, although PCOS constitutes 80% of anovulatory infertility. The risk of very preterm birth in relation to maternal PCOS and hypertensive disorders should be interpreted with caution owing to limited sample sizes. Multifetal pregnancies among maternal PCOS were too few for a subgroup analysis. Moreover, ART included IVF/ICSI only. Potential effects of other treatments, such as ovulation induction, were not examined.
PCOS was associated with additional risks of preterm birth or offspring being LGA in hypertensive mothers, which varied between hypertension types. The exacerbated risks highlight consideration of PCOS in pregnancy counseling and management for women with hypertensive disorders.
STUDY FUNDING/COMPETING INTERESTS: This study was supported by Shandong Provincial Natural Science Foundation, China [ZR2020MH064 to X.C.], the joint research funding of Shandong University and Karolinska Institute [SDU-KI-2019-08 to X.C. and C.L.], the Finnish Institute for Health and Welfare: Drug and pregnancy project [M.G.], the Swedish Research Council [2022-01188 to C.L.], the regional agreement on medical training and clinical research (ALF) between Stockholm County Council and Karolinska Institute Stockholm County Council [RS2021-0855 to C.L.], the Swedish Brain Foundation [FO2021-0412 to C.L.]. The funders had no role in study design, data collection, analysis, and interpretation, writing of the report or decision to submit for publication. The authors report no conflicts of interest.
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多囊卵巢综合征(PCOS)是否与不同高血压类型母亲的巨大儿出生风险及/或早产风险增加有关?
PCOS与慢性高血压母亲及子痫前期母亲单胎妊娠的早产额外风险相关,与妊娠期高血压母亲的大于胎龄儿(LGA)出生风险增加相关。
PCOS女性更易发生妊娠期高血压、子痫前期和慢性高血压。尽管PCOS母亲的不良分娩结局屡有报道,但在高血压疾病背景下的此类关联尚不清楚。
研究设计、规模、持续时间:这是一项基于人群的队列研究,纳入了2004年至2014年芬兰所有的活产儿(n = 652732)。为确保诊断特异性,排除了可能导致类似PCOS体征和症状的诊断母亲。
参与者/材料、设置、方法:从芬兰国家登记处确定母亲的PCOS、妊娠期高血压、慢性高血压和子痫前期诊断。使用广义估计方程和多变量逻辑回归,以无PCOS的血压正常母亲为对照,评估有或无PCOS的高血压母亲早产、极早产以及小于胎龄儿(SGA)或LGA出生的校正比值比(aOR)和95%可信区间(CI)。
在43902名(6.7%)患有高血压疾病的母亲中,1709名(3.9%)患有PCOS。检测到PCOS与高血压在早产、极早产、SGA出生和LGA出生方面存在显著交互作用(分别为χ² = 504.1,P < 0.001;χ² = 124.2,P < 0.001;χ² = 99.5,P < 0.001;χ² = 2.7,P = 0.012)。以无高血压疾病且无PCOS的母亲为对照,慢性高血压或子痫前期的非PCOS母亲早产和极早产风险过高。PCOS与慢性高血压母亲的早产风险增加相关(aOR 4.02,3.14 - 5.15对比aOR 2.51,2.32 - 2.71),暴露之间存在显著交互作用(χ² = 32.7,P < 0.001)。PCOS与子痫前期母亲单胎妊娠的早产风险增加也相关(aOR 7.33,5.92 - 9.06对比aOR 5.72,5.43 - 6.03;χ² = 50.0,P < 0.001)。此外,PCOS合并慢性高血压或子痫前期与自然分娩也有关联。而且,PCOS合并妊娠期高血压母亲的LGA风险较高,尽管单独患有妊娠期高血压的母亲风险较低(aOR 2.04,1.48 - 2.80对比aOR 0.80,0.72 - 0.89;χ² = 9.7,P = 0.002),而对于SGA,有PCOS和无PCOS的高血压母亲风险相当。
局限性、谨慎理由:缺乏药物治疗、子痫前期和妊娠期高血压发病孕周、孕期体重增加以及PCOS表型的信息。所有诊断均从登记处获取,仅代表那些因症状寻求医疗护理的人群。已知1996年前用于识别PCOS的国际疾病分类第九版(ICD - 9)编码会低估PCOS患病率,而将无排卵性不孕纳入PCOS可能会引入高估偏差,尽管PCOS占无排卵性不孕的80%。由于样本量有限,应谨慎解释与母亲PCOS和高血压疾病相关的极早产风险。母亲PCOS中的多胎妊娠过少,无法进行亚组分析。此外,辅助生殖技术(ART)仅包括体外受精/卵胞浆内单精子注射(IVF/ICSI)。未研究其他治疗方法(如促排卵)的潜在影响。
PCOS与高血压母亲的早产或LGA出生额外风险相关,但在不同高血压类型中有所不同。这些加剧的风险凸显了在高血压疾病女性的妊娠咨询和管理中考虑PCOS的重要性。
研究资金/利益冲突:本研究得到中国山东省自然科学基金[ZR2020MH064资助给X.C.]、山东大学与卡罗林斯卡学院联合研究基金[SDU - KI - 2019 - 08资助给X.C.和C.L.]、芬兰健康与福利研究所:药物与妊娠项目[M.G.]、瑞典研究理事会[2022 - 01188资助给C.L.]、斯德哥尔摩郡议会与卡罗林斯卡学院之间的医学培训和临床研究区域协议(ALF)[RS2021 - 0855资助给C.L.]、瑞典脑基金会[FO2021 - 0412资助给C.L.]的支持。资助者在研究设计、数据收集、分析、解释、报告撰写或提交发表的决定中没有作用。作者声明无利益冲突。
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