人类致畸物研究的最新进展。

Teratology Pub Date : 2002-04-01 DOI:10.1002/TERA.10032
Thomas H. Shepard, Robert L. Brent, Jan M. Friedman, Kenneth L. Jones, Richard K. Miller, Cynthia A. Moore, J. Polifka
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引用次数: 101

摘要

背景和方法这篇年度文章的目的是强调和简要回顾可能对孕妇致畸的药物的新的和重要的信息。提供了各种在线和印刷信息来源。结果讨论了以下问题:1)锂药物治疗:降低风险估计;2)吸烟和基因型是导致口腔-面部裂和内翻足的因素;3)甲氧苄氨嘧啶;4)甲巯咪唑综合征;5)糖皮质激素和唇腭裂;6)酗酒;7)胎儿丙戊酸综合征;还有卡马西平。结论:我们强调了几种母亲在怀孕期间暴露与小但增加的出生缺陷率有关,通常每1000名婴儿中只有少数病例。这些暴露包括吸烟和使用锂、甲氧苄啶、甲巯咪唑或皮质类固醇治疗。这种弱致畸效应通常是通过不寻常的治疗与不寻常的出生缺陷结果的联系来确定的。现代流行病学技术的使用,特别是提供更多数据的前瞻性多中心研究,有助于加强这些关联的证据。我们讨论了与背景风险相比很小的致畸风险如何呈现给有风险的妇女和她们的医生。我们简要列出了一些可能用于进一步研究疑似致畸暴露的因素。还给出了各种现有的表达人类致畸性证据强度的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Update on new developments in the study of human teratogens.
BACKGROUND AND METHODS The purpose of this annual article is to highlight and briefly review new and significant information on agents that may be teratogenic in pregnant women. Various sources of on-line and printed information are given. RESULTS The following topics have been discussed: 1) lithium medication: decreased estimate of risk; 2) cigarette smoking and genotype as contributors to oral-facial clefts and clubfoot; 3) trimethoprim; 4) methimazole syndrome?; 5) glucocorticoids and oral-facial clefts; 6) binge drinking; 7) fetal valproate syndrome; and 8) carbamazepine. CONCLUSIONS We have highlighted several maternal exposures during pregnancy that are associated with small but increased rates of birth defects, generally only a few cases per 1,000 infants. These exposures include cigarette smoking, and treatment with lithium, trimethoprim, methimazole, or corticosteroids. This weak teratogenic effect was usually identified by the linkage of an uncommon treatment with an unusual birth defect outcome. The use of modern epidemiologic techniques, especially prospective multicenter studies that provide increased numbers, has helped to strengthen the evidence for these associations. We discuss how teratogenic risks that are small in comparison to the background risk can be presented to at-risk women and their doctors. We have briefly listed some elements that might be used in prioritizing further studies of suspected teratogenic exposures. Various existing methods for expressing the strength of evidence for human teratogenicity are also given.
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