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美国食品和药物管理局批准的在动物身上具有生殖毒性的药物,以及动物试验在人类风险预测中的应用。

FDA-approved drugs that are spermatotoxic in animals and the utility of animal testing for human risk prediction.

机构信息

CLIA Laboratory Director, Birmingham, AL, 35242, USA.

Department of Clinical Laboratory Sciences, Nantong Maternity and Child Health Hospital, Nantong, 226018, China.

出版信息

J Assist Reprod Genet. 2018 Feb;35(2):191-212. doi: 10.1007/s10815-017-1062-8. Epub 2017 Oct 24.

Abstract

PURPOSE

This study reviews FDA-approved drugs that negatively impact spermatozoa in animals, as well as how these findings reflect on observations in human male gametes.

METHODS

The FDA drug warning labels included in the DailyMed database and the peer-reviewed literature in the PubMed database were searched for information to identify single-ingredient, FDA-approved prescription drugs with spermatotoxic effects.

RESULTS

A total of 235 unique, single-ingredient, FDA-approved drugs reported to be spermatotoxic in animals were identified in the drug labels. Forty-nine of these had documented negative effects on humans in either the drug label or literature, while 31 had no effect or a positive impact on human sperm. For the other 155 drugs that were spermatotoxic in animals, no human data was available.

CONCLUSION

The current animal models are not very effective for predicting human spermatotoxicity, and there is limited information available about the impact of many drugs on human spermatozoa. New approaches should be designed that more accurately reflect the findings in men, including more studies on human sperm in vitro and studies using other systems (ex vivo tissue culture, xenograft models, in silico studies, etc.). In addition, the present data is often incomplete or reported in a manner that prevents interpretation of their clinical relevance. Changes should be made to the requirements for pre-clinical testing, drug surveillance, and the warning labels of drugs to ensure that the potential risks to human fertility are clearly indicated.

摘要

目的

本研究回顾了在动物中具有精子毒性的美国食品药品监督管理局(FDA)批准药物,以及这些发现如何反映在人类男性配子中的观察结果。

方法

在 DailyMed 数据库中搜索 FDA 药物警告标签,并在 PubMed 数据库中搜索同行评议文献,以确定具有精子毒性的单一成分、FDA 批准的处方药。

结果

在药物标签中总共发现了 235 种具有动物精子毒性的独特单一成分、FDA 批准的药物。其中 49 种药物在药物标签或文献中记录了对人类有负面影响,而 31 种药物对人类精子没有影响或有积极影响。对于其他 155 种在动物中具有精子毒性的药物,没有人类数据。

结论

目前的动物模型对于预测人类精子毒性并不是非常有效,而且许多药物对人类精子的影响信息有限。应该设计新的方法,更准确地反映男性的发现,包括更多的体外人类精子研究和其他系统(离体组织培养、异种移植模型、计算研究等)的研究。此外,目前的数据往往不完整,或以阻止解释其临床相关性的方式报告。应该对临床前测试、药物监测和药物警告标签的要求进行更改,以确保清楚地表明对人类生育能力的潜在风险。

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