Department of Epidemiology, Harvard T.H. Chan School of Public Health.
Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Brigham and Women's Hospital.
J Hypertens. 2024 Sep 1;42(9):1529-1537. doi: 10.1097/HJH.0000000000003747. Epub 2024 Apr 19.
Although the clinical importance of preeclampsia is widely recognized, few treatment options are available for prevention. TNF-α inhibitors have been hypothesized to potentially prevent the disease. We aimed to examine whether exposure to TNF-α inhibitors during pregnancy reduces the risk of preeclampsia.
We conducted a population-based pregnancy cohort study using nationwide samples of publicly (Medicaid data, 2000-2018) and commercially (MarketScan Research Database, 2003-2020) insured pregnant women linked to their liveborn infants. Exposure was ascertained based on a filled prescription or administration code for TNF-α inhibitors during the first and second trimester of pregnancy. The outcomes included early-onset preeclampsia, late-onset preeclampsia, and small-for-gestational age. For baseline confounding adjustment, we leveraged propensity score overlap weights to estimate risk ratios (RR).
Among 4 315 658 pregnancies in the Medicaid and the MarketScan cohort, 2736 (0.063%) were exposed to TNF-α inhibitors during the first trimester and 1712 (0.040%) during the second trimester. After adjustment, the risk of early-onset preeclampsia was not decreased among mothers exposed during the first trimester compared with unexposed women with treatment indications [RR pooled : 1.25, 95% confidence interval (CI) 0.93-1.67]. Similarly, the risk of late-onset preeclampsia was not decreased among mothers exposed during the second trimester compared with unexposed women (RR pooled : 0.99, 95% CI 0.81-1.22).
Contrary to the hypothesis, exposure to TNF-α inhibitors during pregnancy did not appear to be associated with a reduced risk of early-onset or late-onset preeclampsia. These findings do not support consideration of the use of TNF-α inhibitors for the prevention of preeclampsia.
虽然子痫前期的临床重要性已被广泛认识,但目前可用的治疗方法很少。TNF-α 抑制剂已被假设可能预防该疾病。我们旨在研究妊娠期间暴露于 TNF-α 抑制剂是否降低子痫前期的风险。
我们进行了一项基于人群的妊娠队列研究,使用了公共(医疗补助数据,2000-2018 年)和商业(MarketScan 研究数据库,2003-2020 年)保险的孕妇全国样本,并与她们的活产婴儿相关联。暴露情况根据妊娠第一和第二孕期 TNF-α 抑制剂的处方或管理代码确定。结局包括早发型子痫前期、晚发型子痫前期和胎儿生长受限。为了进行基线混杂因素调整,我们利用倾向评分重叠权重来估计风险比(RR)。
在 Medicaid 和 MarketScan 队列中,4315658 例妊娠中,有 2736 例(0.063%)在妊娠第一孕期暴露于 TNF-α 抑制剂,有 1712 例(0.040%)在妊娠第二孕期暴露。调整后,与有治疗指征的未暴露妇女相比,第一孕期暴露 TNF-α 抑制剂的母亲发生早发型子痫前期的风险并未降低[汇总 RR:1.25,95%置信区间(CI)0.93-1.67]。同样,与未暴露妇女相比,第二孕期暴露 TNF-α 抑制剂的母亲发生晚发型子痫前期的风险也没有降低[汇总 RR:0.99,95%CI 0.81-1.22]。
与假设相反,妊娠期间暴露于 TNF-α 抑制剂似乎与降低早发型或晚发型子痫前期的风险无关。这些发现不支持考虑使用 TNF-α 抑制剂预防子痫前期。