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母体暴露于唑吡坦与特定出生缺陷风险。

Maternal exposure to zolpidem and risk of specific birth defects.

机构信息

New York State Department of Health, Birth Defects Registry, Albany, New York, USA.

Department of Epidemiology, Boston University School of Public Health, Boston, Massachusetts, USA.

出版信息

J Sleep Res. 2024 Feb;33(1):e13958. doi: 10.1111/jsr.13958. Epub 2023 Jun 2.

Abstract

Zolpidem is a non-benzodiazepine agent indicated for treatment of insomnia. While zolpidem crosses the placenta, little is known about its safety in pregnancy. We assessed associations between self-reported zolpidem use 1 month before pregnancy through to the end of the third month ("early pregnancy") and specific birth defects using data from two multi-site case-control studies: National Birth Defects Prevention Study and Slone Epidemiology Center Birth Defects Study. Analysis included 39,711 birth defect cases and 23,035 controls without a birth defect. For defects with ≥ 5 exposed cases, we used logistic regression with Firth's penalised likelihood to estimate adjusted odds ratios and 95% confidence intervals, considering age at delivery, race/ethnicity, education, body mass index, parity, early-pregnancy antipsychotic, anxiolytic, antidepressant use, early-pregnancy opioid use, early-pregnancy smoking, and study as potential covariates. For defects with three-four exposed cases, we estimated crude odds ratios and 95% confidence intervals. Additionally, we explored differences in odds ratios using propensity score-adjustment and conducted a probabilistic bias analysis of exposure misclassification. Overall, 84 (0.2%) cases and 46 (0.2%) controls reported early-pregnancy zolpidem use. Seven defects had sufficient sample size to calculate adjusted odds ratios, which ranged from 0.76 for cleft lip to 2.18 for gastroschisis. Four defects had odds ratios > 1.8. All confidence intervals included the null. Zolpidem use was rare. We could not calculate adjusted odds ratios for most defects and estimates are imprecise. Results do not support a large increase in risk, but smaller increases in risk for certain defects cannot be ruled out.

摘要

唑吡坦是一种非苯二氮䓬类药物,用于治疗失眠症。虽然唑吡坦可穿过胎盘,但关于其在妊娠期间的安全性知之甚少。我们利用两项多地点病例对照研究(国家出生缺陷预防研究和斯隆流行病学中心出生缺陷研究)的数据,评估了在妊娠前 1 个月至妊娠 3 个月末(“早期妊娠”)自我报告的唑吡坦使用与特定出生缺陷之间的关联。分析包括 39711 例出生缺陷病例和 23035 例无出生缺陷对照。对于≥5 例暴露病例的缺陷,我们使用逻辑回归和 Firth 罚似然法来估计调整后的优势比和 95%置信区间,同时考虑分娩时的年龄、种族/民族、教育程度、体重指数、产次、妊娠早期抗精神病药、抗焦虑药、抗抑郁药的使用、妊娠早期阿片类药物的使用、妊娠早期吸烟和研究作为潜在的协变量。对于有三到四个暴露病例的缺陷,我们估计了粗优势比和 95%置信区间。此外,我们还通过倾向评分调整来探索了优势比的差异,并对暴露错误分类进行了概率偏差分析。总的来说,84 例(0.2%)病例和 46 例(0.2%)对照报告了妊娠早期使用唑吡坦。有 7 种缺陷的样本量足以计算调整后的优势比,范围从唇裂的 0.76 到脐膨出的 2.18。有 4 种缺陷的优势比>1.8。所有置信区间均包含零。唑吡坦的使用非常罕见。我们无法为大多数缺陷计算调整后的优势比,且估计值不够精确。结果不支持风险大幅增加,但不能排除某些缺陷的风险略有增加。

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