探讨胎儿性别作为妊娠期睡眠呼吸障碍及其并发症的危险因素。

Gender and the Genome Pub Date : 2020-01-01 Epub Date: 2020-08-21 DOI:10.1177/2470289720948076
Margaret H Bublitz, Myriam Salameh, Laura Sanapo, Ghada Bourjeily
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引用次数: 0

摘要

睡眠呼吸障碍(SDB)是一种常见的妊娠期疾病,但未被充分认识和治疗。睡眠呼吸障碍与妊娠并发症有关,包括先兆子痫、妊娠糖尿病、早产以及严重的孕产妇发病率和死亡率。妊娠期SDB危险因素的识别可以改善妊娠并发症发生前SDB的筛查、诊断和治疗。本研究的目的是确定胎儿性别是否会增加妊娠期SDB的风险。选取分娩24 ~ 48小时内的单胎孕妇(N = 991)为研究对象,采用问卷方式回答有关SDB症状的问题。每周至少三次频繁大声打鼾的女性被认为患有SDB。我们回顾了医院记录,以提取胎儿性别和妊娠并发症的信息,包括先兆子痫、妊娠高血压、妊娠糖尿病、早产和低出生体重。怀男性胎儿的妇女患SDB的可能性显著增加(β = 0.37, P = 0.01, OR: 1.45 [95% CI: 1.09-1.94])。胎儿性别与妊娠期患有SDB的妇女发生妊娠高血压疾病(定义为子痫前期和/或妊娠高血压)的风险增加相关(β = 0.41, P = 0.02, or: 1.51[95%CI:1.08-2.11])。胎儿性别不会增加妊娠期SDB患者的早产、低出生体重或妊娠糖尿病的风险。怀孕期间携带男性胎儿的妇女报告SDB的可能性是携带女性胎儿的妇女的1.5倍,携带男性胎儿的妊娠期发病SDB的妇女患妊娠期高血压疾病的可能性是携带女性胎儿的妇女的1.5倍。确认胎儿性别是一个危险因素,可能与其他危险因素一起,在确定怀孕期间SDB并发症风险最高的妇女中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploring Fetal Sex as a Risk Factor for Sleep Disordered Breathing and Its Complications in Pregnancy.

Exploring Fetal Sex as a Risk Factor for Sleep Disordered Breathing and Its Complications in Pregnancy.

Sleep disordered breathing (SDB) is a common, yet under-recognized and undertreated condition in pregnancy. Sleep disordered breathing is associated with pregnancy complications including preeclampsia, gestational diabetes, preterm birth, as well as severe maternal morbidity and mortality. The identification of risk factors for SDB in pregnancy may improve screening, diagnosis, and treatment of SDB prior to the onset of pregnancy complications. The goal of this study was to determine whether fetal sex increases risk of SDB in pregnancy. A cohort of singleton (N = 991) pregnant women were recruited within 24 to 48 hours of delivery and answered questions regarding SDB symptoms by questionnaire. Women who reported frequent loud snoring at least 3 times a week were considered to have SDB. Hospital records were reviewed to extract information on fetal sex and pregnancy complications including preeclampsia, pregnancy-induced hypertension, gestational diabetes, preterm delivery, and low birth weight. Women carrying male fetuses were significantly more likely to have SDB (β = .37, P = .01, OR: 1.45 [95% CI: 1.09-1.94]). Fetal sex was associated with increased risk of hypertensive disorders of pregnancy (defined as preeclampsia and/or pregnancy-induced hypertension) among women with SDB in pregnancy (β = .41, P = .02, OR: 1.51[95%CI:1.08-2.11]).Fetal sex did not increase risk of preterm birth, low birth weight, or gestational diabetes among women with SDB in pregnancy. Women carrying male fetuses were approximately 1.5 times more likely to report SDB in pregnancy compared to women carrying female fetuses, and women with pregnancy-onset SDB carrying male fetuses were 1.5 times more likely to have hypertensive disorders of pregnancy compared to women with SDB carrying female fetuses. Confirmation of fetal sex as a risk factor may, with other risk factors, play a role in identifying women at highest risk of SDB complications in pregnancy.

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