Facco Francesca L, Grobman William A, Reid Kathryn J, Parker Corette B, Hunter Shannon M, Silver Robert M, Basner Robert C, Saade George R, Pien Grace W, Manchanda Shalini, Louis Judette M, Nhan-Chang Chia-Ling, Chung Judith H, Wing Deborah A, Simhan Hyagriv N, Haas David M, Iams Jay, Parry Samuel, Zee Phyllis C
Department of Obstetrics and Gynecology, Magee-Womens Research Institute and Foundation, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Northwestern University Feinberg School of Medicine, Chicago, IL.
Am J Obstet Gynecol. 2017 Oct;217(4):447.e1-447.e13. doi: 10.1016/j.ajog.2017.05.066. Epub 2017 Jun 7.
Experimental and epidemiologic data suggest that among nonpregnant adults, sleep duration may be an important risk factor for chronic disease. Although pregnant women commonly report poor sleep, few studies objectively evaluated the quality of sleep in pregnancy or explored the relationship between sleep disturbances and maternal and perinatal outcomes.
Our objective was to examine the relationship between objectively assessed sleep duration, timing, and continuity (measured via wrist actigraphy) and maternal cardiovascular and metabolic morbidity specific to pregnancy.
This was a prospective cohort study of nulliparous women. Women were recruited between 16 0/7 and 21 6/7 weeks' gestation. They were asked to wear a wrist actigraphy monitor and complete a daily sleep log for a period of 7 consecutive days. The primary sleep exposure variables were the averages of the following over the total valid nights (minimum 5, maximum 7 nights): short sleep duration during the primary sleep period (<7 h/night), late sleep midpoint (midpoint between sleep onset and sleep offset >5 am), and top quartile of minutes of wake time after sleep onset and sleep fragmentation index. The primary outcomes of interest were a composite of hypertensive disorders of pregnancy (mild, severe, or superimposed preeclampsia; eclampsia; or antepartum gestational hypertension) and gestational diabetes mellitus. We used χ tests to assess associations between sleep variables and categorical baseline characteristics. Crude odds ratios and 95% confidence intervals were estimated from univariate logistic regression models to characterize the magnitude of the relationship between sleep characteristics and hypertensive disorders of pregnancy and gestational diabetes. For associations significant in univariate analysis, multiple logistic regression was used to explore further the association of sleep characteristics with pregnancy outcomes.
In all, 901 eligible women consented to participate; 782 submitted valid actigraphy studies. Short sleep duration and a later sleep midpoint were associated with an increased risk of gestational diabetes (odds ratio, 2.24; 95% confidence interval, 1.11-4.53; and odds ratio, 2.58; 95% confidence interval, 1.24-5.36, respectively) but not of hypertensive disorders. A model with both sleep duration and sleep midpoint as well as their interaction term revealed that while there was no significant interaction between these exposures, the main effects of both short sleep duration and later sleep midpoint with gestational diabetes remained significant (adjusted odds ratio, 2.06; 95% confidence interval, 1.01-4.19; and adjusted odds ratio, 2.37; 95% confidence interval, 1.13-4.97, respectively). Additionally, after adjusting separately for age, body mass index, and race/ethnicity, both short sleep duration and later sleep midpoint remained associated with gestational diabetes. No associations were demonstrated between the sleep quality measures (wake after sleep onset, sleep fragmentation) and hypertensive disorders or gestational diabetes.
Our results demonstrate a relationship between short sleep duration and later sleep midpoint with gestational diabetes. Our data suggest independent contributions of these 2 sleep characteristics to the risk for gestational diabetes in nulliparous women.
实验和流行病学数据表明,在非孕成年人中,睡眠时间可能是慢性病的一个重要危险因素。虽然孕妇普遍反映睡眠质量差,但很少有研究客观评估孕期睡眠质量,或探究睡眠障碍与孕产妇及围产期结局之间的关系。
我们的目的是研究通过手腕活动记录仪客观评估的睡眠时间、时间点和连续性与孕期特有的孕产妇心血管和代谢疾病之间的关系。
这是一项针对未生育女性的前瞻性队列研究。在妊娠16 0/7至21 6/7周期间招募女性。要求她们佩戴手腕活动记录仪,并连续7天完成每日睡眠日志。主要睡眠暴露变量是在所有有效夜间(最少5晚,最多7晚)以下各项的平均值:主要睡眠期的短睡眠时间(<7小时/晚)、晚睡中点(入睡和起床之间的中点>上午5点),以及入睡后清醒时间的前四分位数和睡眠片段化指数。感兴趣的主要结局是妊娠高血压疾病(轻度、重度或叠加先兆子痫;子痫;或产前妊娠高血压)和妊娠期糖尿病的综合情况。我们使用χ检验评估睡眠变量与分类基线特征之间的关联。从单变量逻辑回归模型估计粗比值比和95%置信区间,以描述睡眠特征与妊娠高血压疾病和妊娠期糖尿病之间关系的强度。对于单变量分析中有显著意义的关联,使用多变量逻辑回归进一步探究睡眠特征与妊娠结局之间的关联。
总共901名符合条件的女性同意参与;782名提交了有效的活动记录仪研究数据。短睡眠时间和晚睡中点与妊娠期糖尿病风险增加相关(比值比分别为2.24;95%置信区间为1.11 - 4.53;以及比值比为2.58;95%置信区间为1.24 - 5.36),但与妊娠高血压疾病无关。一个同时包含睡眠时间和睡眠中点及其交互项的模型显示,虽然这些暴露之间没有显著交互作用,但短睡眠时间和晚睡中点与妊娠期糖尿病的主要效应仍然显著(调整后比值比分别为2.06;95%置信区间为1.01 - 4.19;以及调整后比值比为2.37;95%置信区间为1.13 - 4.97)。此外,在分别调整年龄、体重指数和种族/族裔后,短睡眠时间和晚睡中点仍然与妊娠期糖尿病相关。睡眠质量指标(入睡后清醒、睡眠片段化)与妊娠高血压疾病或妊娠期糖尿病之间未显示出关联。
我们的结果表明短睡眠时间和晚睡中点与妊娠期糖尿病之间存在关联。我们的数据表明这两个睡眠特征对未生育女性患妊娠期糖尿病的风险有独立影响。