4.6 Article

Changes in Sertraline Plasma Concentrations Across Pregnancy and Postpartum

期刊

CLINICAL PHARMACOLOGY & THERAPEUTICS
卷 112, 期 6, 页码 1280-1290

出版社

WILEY
DOI: 10.1002/cpt.2746

关键词

-

资金

  1. Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) [U54HD047891, U54HD047905, U54HD085601]
  2. National Institute of Health (NIH) [UL1TR001439]
  3. Obstetric-Fetal Pharmacology Research Center (OPRC)
  4. Asher Center for the Study and Treatment of Depressive Disorders
  5. Center for Pharmacogenomics
  6. Northwestern University Feinberg School of Medicine
  7. NIH's National Center for Advancing Translational Sciences [UL1TR001422]
  8. Mary Beth Donnelley Clinical Pharmacology Core Facility at Northwestern University
  9. NIH [S10 OD021786]
  10. NICHD [1U54HD085601-01]

向作者/读者索取更多资源

This study aimed to investigate the pharmacokinetics of sertraline during pregnancy and the impact of pharmacogenetic variability on its elimination. The results showed that the ratio of sertraline concentration to dose decreased during pregnancy and was associated with CYP2C19 activity.
Major depressive disorder (MDD) is a common disorder in pregnancy. Although sertraline is the most frequently prescribed antidepressant for pregnant people in the United States, limited information about its pharmacokinetics in pregnancy is available. Our objectives were to characterize plasma sertraline concentration to dose (C/D) ratios across pregnancy and postpartum and investigate the effect of pharmacogenetic variability on sertraline elimination. We performed a prospective observational cohort study in people with a singleton pregnancy <= 18 weeks gestation and a lifetime diagnosis of MDD at the 3 Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)-funded Obstetrical-Fetal Pharmacology Research Center sites. Subjects (N = 47) were receiving maintenance sertraline therapy and chose to continue it during pregnancy. Blood samples were obtained 24-hours postdose every 4 weeks across pregnancy and twice postpartum for measurement of plasma concentrations of sertraline and desmethylsertraline. Overall mean sertraline C/D ratios were decreased at study onset and remained consistently low until after delivery. During the last 4 weeks of pregnancy the mean sertraline C/D ratio (95% confidence interval (CI)), 0.25 (95% CI, 0.19, 0.3) ng/mL/dose (mg/day), was smaller than the mean ratio at >= 8 weeks after delivery, 0.32 (95% CI, 0.27, 0.37) ng/mL/dose (mg/day), a 22% difference. Mean sertraline/desmethylsertraline ratios were highest after birth, which confirmed increased sertraline elimination during pregnancy. Sertraline C/D ratios in participants with functional CYP2C19 activity did not change significantly during pregnancy, whereas ratios in participants with poor or intermediate CYP2C19 activity decreased by 51%. Exploratory pharmacogenomic analysis indicated that pregnant people with poor or intermediate CYP2C19 activity are at risk for subtherapeutic sertraline concentrations during pregnancy.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据