Department of Epidemiology, Biostatistics and HTA, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
PLoS One. 2011;6(7):e22174. doi: 10.1371/journal.pone.0022174. Epub 2011 Jul 18.
Since use of non-steroidal anti-inflammatory drugs (NSAIDs) during pregnancy is common, small increases in the risk of birth defects may have significant implications for public health. Results of human studies on the teratogenic risks of NSAIDs are inconsistent. Therefore, we evaluated the risk of selected birth defects after prenatal exposure to prescribed and over-the-counter NSAIDs.
We used data on 69,929 women enrolled in the Norwegian Mother and Child Cohort Study between 1999 and 2006. Data on NSAID exposure were available from a self-administered questionnaire completed around gestational week 17. Information on pregnancy outcome was obtained from the Medical Birth Registry of Norway. Only birth defects suspected to be associated with NSAID exposure based upon proposed teratogenic mechanisms and previous studies were included in the multivariable logistic regression analyses. A total of 3,023 women used NSAIDs in gestational weeks 0-12 and 64,074 women did not report NSAID use in early pregnancy. No associations were observed between overall exposure to NSAIDs during pregnancy and the selected birth defects separately or as a group (adjusted odds ratio 0.7, 95% confidence interval 0.4-1.1). Associations between maternal use of specific types of NSAIDs and the selected birth defects were not found either, although an increased risk was seen for septal defects and exposure to multiple NSAIDs based on small numbers (2 exposed cases; crude odds ratio 3.9, 95% confidence interval 0.9-15.7).
Exposure to NSAIDs during the first 12 weeks of gestation does not seem to be associated with an increased risk of the selected birth defects. However, due to the small numbers of NSAID-exposed infants for the individual birth defect categories, increases in the risks of specific birth defects could not be excluded.
由于孕妇使用非甾体抗炎药(NSAIDs)很常见,因此出生缺陷风险的微小增加可能对公共卫生具有重大意义。人类研究关于 NSAIDs 的致畸风险的结果并不一致。因此,我们评估了产前暴露于处方和非处方 NSAIDs 后选定的出生缺陷风险。
我们使用了 1999 年至 2006 年间参加挪威母亲和儿童队列研究的 69929 名女性的数据。NSAID 暴露数据可从妊娠第 17 周左右完成的自我管理问卷中获得。挪威医学出生登记处提供了妊娠结局的信息。只有根据提出的致畸机制和先前的研究怀疑与 NSAID 暴露相关的出生缺陷才包括在多变量逻辑回归分析中。共有 3023 名女性在妊娠 0-12 周使用 NSAIDs,64074 名女性未报告早期妊娠使用 NSAIDs。怀孕期间总体暴露于 NSAIDs 与选定的出生缺陷之间没有观察到关联,分别或作为一组观察到(调整后的优势比 0.7,95%置信区间 0.4-1.1)。也没有发现母亲使用特定类型的 NSAIDs 与选定的出生缺陷之间存在关联,尽管根据少数病例(2 个暴露病例;粗优势比 3.9,95%置信区间 0.9-15.7),观察到间隔缺陷和暴露于多种 NSAIDs 的风险增加。
妊娠前 12 周暴露于 NSAIDs 似乎不会增加选定的出生缺陷风险。然而,由于特定出生缺陷类别的 NSAID 暴露婴儿数量较少,不能排除特定出生缺陷风险增加的可能性。