Post-Conceptional Exposure to Clomiphene Citrate and Congenital Malformations: A Cohort Study.

IF 4 2区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Safety Pub Date : 2024-09-01 Epub Date: 2024-05-13 DOI:10.1007/s40264-024-01438-0
Rebeccah Nehard, Catherine Vauzelle, Delphine Beghin, Mathilde Latour, Elisabeth Elefant, Bénédicte Coulm, Benoît Marin
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Abstract

Background: Clomiphene citrate is an ovulation inductor for which inadvertent post-conceptional exposures may occur in early pregnancy. In preclinical studies, post-conceptional exposures showed a teratogenic effect in different species. In humans, to date, little is known about the outcomes of inadvertently post-conceptionally exposed pregnancies.

Objectives: The objectives of our study were to assess the association between post-conceptional exposures to clomiphene citrate and major and minor congenital malformations in the offspring.

Methods: A retrospective cohort study of prospectively ascertained cases was undertaken, based on clinical data from the Centre de Référence sur les Agents Tératogènes (CRAT), Paris, France. Women with post-conceptional exposure to clomiphene citrate (n = 309), and unexposed pregnant women (n = 1236, 1:4 ratio) with prospectively collected data, known pregnancy outcome and delivery date prior to 01/02/2022, were matched by calendar year. An adjudication committee classified major and minor congenital malformations according to the EUROCAT (European Registration of Congenital Anomalies and Twins) classification.

Results: Among post-conceptional exposed women, no increased risk of major malformation was found (crude relative risk = 0.64, 95% confidence interval 0.19-2.15) as compared to unexposed women. Three major and ten minor congenital malformations were reported in the exposed group. An increased risk of minor malformations was found (crude relative risk = 4.05, 95% confidence interval 1.70-9.64) although there was no specific clinical pattern.

Conclusions: Post-conceptional exposure to clomiphene citrate was not associated with an increased risk of major congenital malformations. Given potential confounding and information biases, the results about minor malformations should be interpreted with caution as no specific clinical pattern was identified.

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枸橼酸氯米芬受孕后暴露与先天性畸形:一项队列研究。
背景:枸橼酸氯米芬是一种排卵诱导剂,在怀孕早期可能会无意中发生受孕后接触。在临床前研究中,不同物种的受孕后暴露显示出致畸效应。迄今为止,人们对人类意外受孕后妊娠的结果知之甚少:我们的研究目的是评估受孕后接触枸橼酸氯米芬与后代主要和次要先天性畸形之间的关系:根据法国巴黎妊娠药物研究中心(CRAT)的临床数据,对前瞻性确定的病例进行了一项回顾性队列研究。按日历年对受孕后接触过枸橼酸氯米芬的妇女(n = 309)和未接触过枸橼酸氯米芬的孕妇(n = 1236,比例为 1:4)进行了配对,前者拥有前瞻性收集的数据、已知的妊娠结果和 2022 年 2 月 1 日之前的分娩日期。评审委员会根据欧洲先天性畸形和双胞胎登记分类法(EUROCAT)对主要先天性畸形和次要先天性畸形进行了分类:与未受孕妇女相比,受孕后暴露的妇女发生重大畸形的风险没有增加(粗略相对风险 = 0.64,95% 置信区间为 0.19-2.15)。据报告,暴露组中有 3 例重大先天畸形和 10 例轻微先天畸形。虽然没有特定的临床模式,但发现轻微畸形的风险增加(粗略相对风险 = 4.05,95% 置信区间为 1.70-9.64):结论:受孕后接触枸橼酸氯米芬与重大先天性畸形风险增加无关。考虑到潜在的混杂因素和信息偏差,由于没有发现特定的临床模式,因此应谨慎解释有关轻微畸形的结果。
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来源期刊
Drug Safety
Drug Safety 医学-毒理学
CiteScore
7.60
自引率
7.10%
发文量
112
审稿时长
6-12 weeks
期刊介绍: Drug Safety is the official journal of the International Society of Pharmacovigilance. The journal includes: Overviews of contentious or emerging issues. Comprehensive narrative reviews that provide an authoritative source of information on epidemiology, clinical features, prevention and management of adverse effects of individual drugs and drug classes. In-depth benefit-risk assessment of adverse effect and efficacy data for a drug in a defined therapeutic area. Systematic reviews (with or without meta-analyses) that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. Original research articles reporting the results of well-designed studies in disciplines such as pharmacoepidemiology, pharmacovigilance, pharmacology and toxicology, and pharmacogenomics. Editorials and commentaries on topical issues. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Drug Safety Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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