孕期抗逆转录病毒药物暴露与先天畸形风险:欧洲病例/非病例畸形研究。

IF 2.4 3区 医学 Q3 PHARMACOLOGY & PHARMACY
Laura Saint-Lary, Anna-Belle Beau, Agnès Sommet, Valériane Leroy, Maria Loane, Clara Cavero-Carbonell, Ester Garne, Jonathan Hoareau, Anna Latos Bielenska, Isabelle Monier, Vera Nelen, Amanda J Neville, Mary O'Mahony, Isabelle Perthus, Anna Pierini, Anke Rissmann, Florence Rouget, Joanna Sichitiu, David Tucker, Helen Dolk, Christine Damase-Michel
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引用次数: 0

摘要

目的:建议在怀孕期间使用抗逆转录病毒药物,以抑制艾滋病毒,减少母婴传播。在几项研究中,胎儿暴露于抗逆转录病毒药物后报告了先天性异常信号,值得进一步调查。我们的目的是评估胎儿暴露于抗逆转录病毒药物后先天性异常的风险,使用欧洲先天性异常登记数据。方法:使用EUROmediCAT中央数据库进行病例/非病例研究。所有暴露于抗逆转录病毒药物的先天性异常都包括在1995年至2019年期间。我们探索了从文献中确定的先天性异常和特定抗逆转录病毒暴露之间的关联的每个信号。我们比较了信号异常(病例)和所有其他畸形登记(对照)之间的抗逆转录病毒暴露。估计报告优势比(ROR)及其95%置信区间,并根据登记和产妇年龄进行调整。结果:1995年至2019年,173例暴露于抗逆转录病毒药物后出现先天性异常。先前在文献中发现的先天性心脏缺陷与齐多夫定暴露之间的信号在主要分析中得到证实(aROR 3.66[1.63-8.23])。虽然在齐多夫定和阿扎那韦暴露后分别报道了2例尿道下裂和2例肢体缺陷,但文献中发现的其他信号尚未得到证实。经Bonferroni校正后,信号检测分析未发现新的信号。结论:我们的研究没有揭示新的信号,但证实了先前发现的先天性心脏缺陷和胎儿暴露于齐多夫定之间的信号。齐多夫定暴露引起的生理病理假说有待进一步探讨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antiretroviral drug exposure in pregnancy and risk of congenital anomalies: a European case/non-case malformed study.

Purpose: Antiretroviral drugs are recommended during pregnancy to achieve HIV viral suppression and reduce mother-to-child transmission. Congenital anomaly signals were reported after fetal exposure to antiretroviral drugs in several studies warranting further investigation. We aimed to evaluate the risk of congenital anomalies after fetal exposure to antiretroviral drugs using the European congenital anomaly registry data.

Methods: A case/non-case study was performed, using the EUROmediCAT central database. All the congenital anomalies, exposed to any antiretroviral drugs, were included from 1995 to 2019. We explored each signal identified from the literature for associations between congenital anomalies and specific antiretroviral exposures. We compared antiretroviral exposure between the signal anomalies (cases) and all other malformed registrations (controls). Reporting odds ratio (ROR) and their 95% confidence intervals were estimated and adjusted for registry and maternal age.

Results: Between 1995 and 2019, 173 cases of congenital anomalies were observed after any exposure to antiretroviral drugs. The signal previously identified in the literature between congenital heart defects and exposure to zidovudine was confirmed in the main analysis (aROR 3.66 [1.63-8.23]). Other signals identified in the literature were not confirmed, although two cases of hypospadias and two cases of limb defects were reported after zidovudine and atazanavir exposure, respectively. The signal detection analysis did not reveal any new signal after applying the Bonferroni correction.

Conclusions: Our study does not reveal new signals but confirms the previously identified signal between congenital heart defects and fetal exposure to zidovudine. The physio-pathological hypothesis induced by zidovudine exposure should be explored in future studies.

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来源期刊
CiteScore
5.40
自引率
3.40%
发文量
170
审稿时长
3-8 weeks
期刊介绍: The European Journal of Clinical Pharmacology publishes original papers on all aspects of clinical pharmacology and drug therapy in humans. Manuscripts are welcomed on the following topics: therapeutic trials, pharmacokinetics/pharmacodynamics, pharmacogenetics, drug metabolism, adverse drug reactions, drug interactions, all aspects of drug development, development relating to teaching in clinical pharmacology, pharmacoepidemiology, and matters relating to the rational prescribing and safe use of drugs. Methodological contributions relevant to these topics are also welcomed. Data from animal experiments are accepted only in the context of original data in man reported in the same paper. EJCP will only consider manuscripts describing the frequency of allelic variants in different populations if this information is linked to functional data or new interesting variants. Highly relevant differences in frequency with a major impact in drug therapy for the respective population may be submitted as a letter to the editor. Straightforward phase I pharmacokinetic or pharmacodynamic studies as parts of new drug development will only be considered for publication if the paper involves -a compound that is interesting and new in some basic or fundamental way, or -methods that are original in some basic sense, or -a highly unexpected outcome, or -conclusions that are scientifically novel in some basic or fundamental sense.
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