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人类致畸物及其对发育中大脑的影响的范围综述:来自ConcePTION项目的贡献。

A Scoping Review of Human Teratogens and Their Impact on the Developing Brain: A Contribution From the ConcePTION Project.

作者信息

Bluett-Duncan M, Adams J, Berkovitch M, Berlin M, Cahoon A, Clayton-Smith J, Jackson C, Khanom S, Mølgaard-Nielsen D, Richardson J L, Simms V, Stellfeld M, Winterfeld U, Yates L M, Bromley R L

机构信息

Division of Neuroscience, School of Biological Sciences, The University of Manchester, Manchester, UK.

Department of Psychology, University of Massachusetts Boston, Boston, MA, USA.

出版信息

Birth Defects Res. 2025 Sep;117(9):e2497. doi: 10.1002/bdr2.2497.

Abstract

Certain medications, when used during pregnancy, are known to impact human prenatal development. Historically, little attention has been given to the impact of in utero exposure on the developing brain, despite the significance of known teratogen-induced neurodevelopmental difficulties. This scoping review systematically identified and extracted neurodevelopmental outcome data for medications with established physical teratogenic effects and synthesized the key study characteristics. Medications with evidence of physical teratogenicity (n = 24) were defined by a panel of experts. Eligible studies reporting any neurodevelopmental outcomes following pregnancy exposure to the defined list of human structural teratogens were identified through electronic searches of MEDLINE and EMBASE. We identified 207 studies (254 publications) for inclusion, comprising 81 empirical cohorts and 126 case series. Concerningly, only 13 of 24 (54%) confirmed structural teratogens have been subject to any empirical investigation of neurodevelopmental outcomes. The mean time between authorization of known structural teratogens and the first empirical study investigating neurodevelopmental outcomes using a comparison group and formal data analysis is 33 years (Range: 11-64 years). When neurodevelopmental outcomes are investigated for medication exposures with physical teratogenic signatures, there are high levels of neurodevelopmental alterations (77%). These findings do not speak to a pharmacovigilance system that is functioning efficiently to identify and ameliorate neurodevelopmental risk, even for the medications with identified structural teratogenic risk. Given the high proportion of known physical teratogens exhibiting additional altered neurodevelopmental outcomes and the substantial lifetime burden of such alterations, to the individual and society, the timelines remain too long.

摘要

某些药物在孕期使用时,已知会影响人类产前发育。从历史上看,尽管已知致畸剂会导致神经发育困难,但子宫内暴露对发育中大脑的影响却很少受到关注。本范围综述系统地识别并提取了具有已确定身体致畸作用的药物的神经发育结局数据,并综合了关键研究特征。一组专家定义了具有身体致畸证据的药物(n = 24)。通过对MEDLINE和EMBASE进行电子检索,确定了符合条件的研究,这些研究报告了孕期暴露于已定义的人类结构致畸剂列表后出现的任何神经发育结局。我们确定了207项研究(254篇出版物)纳入,包括81个实证队列和126个病例系列。令人担忧的是,24种已确认的结构致畸剂中只有13种(54%)接受了任何关于神经发育结局的实证研究。已知结构致畸剂获批与第一项使用对照组和正式数据分析来研究神经发育结局的实证研究之间的平均时间为33年(范围:11 - 64年)。当研究具有身体致畸特征的药物暴露的神经发育结局时,神经发育改变的发生率很高(77%)。这些发现表明,即使对于已确定具有结构致畸风险的药物,药物警戒系统也未能有效运作以识别和改善神经发育风险。鉴于已知的身体致畸剂中有很大比例表现出额外的神经发育改变,且这种改变给个人和社会带来了巨大的终生负担,目前的时间线仍然过长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7467/12442749/2a49159ba53c/BDR2-117-e2497-g006.jpg

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