Enhancing reliability of embryo-fetal developmental toxicity studies: A proposed design of replicate studies.

IF 3 4区 医学 Q1 MEDICINE, LEGAL
L David Wise
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引用次数: 0

Abstract

Background: This report addresses the reliability of results from rat Embryo-Fetal Developmental Toxicity (EFDT) studies. Recent literature discusses the roles of reproducibility, replicability, and other influences on scientific reliability. Reproducibility is a re-analysis of the original data, while replicability addresses the same question with a separate study of some type. Concordance of rat and rabbit studies has been addressed previously, but replication of single-species EFDT studies was not found in the literature. A modest modification of the rat study is therefore proposed to assess replicability and possibly enhance reliability.

Methods: Regulatory guidelines were consulted and relevant literature was identified through online searches.

Results: Each replicate EFDT (r-EFDT) study in rats would consist of half the mated females of the definitive study. Studies would start at the same or different times in one testing facility. Separate shipments of animals (non-littermates) are required. All other procedures would be protocol-driven. The micro- and macro-environments of the animals would be held as constant as possible. Justification, design options, and interpretation methods are discussed.

Conclusion: Besides adding reliability, other benefits include reduced animal usage, and potentially reduced cost and time to final reports. By reducing the need for repeated studies due to questionable results, this modified study is viewed as a more efficient use of costly resources. The r-EFDT study design could easily be adapted to assess replicability of rabbit EFDT and some general toxicity studies. Future replicate studies are needed to critically evaluate replicability and the overall impact on study reliability.

提高胚胎-胎儿发育毒性研究的可靠性:拟议的重复研究设计
背景:本报告探讨了大鼠胚胎-胎儿发育毒性(EFDT)研究结果的可靠性。最近的文献讨论了可重复性、可复制性以及对科学可靠性的其他影响因素的作用。可重复性是对原始数据的重新分析,而可复制性则是通过某种类型的单独研究来解决同一问题。以前曾讨论过大鼠和兔子研究的一致性,但在文献中没有发现单物种 EFDT 研究的可复制性。因此,建议对大鼠研究进行适度修改,以评估可重复性并可能提高可靠性:方法:参考监管指南,并通过在线搜索确定相关文献:在大鼠中进行的每项重复 EFDT(r-EFDT)研究将由最终研究中交配雌鼠的一半组成。研究将在同一试验设施的相同或不同时间开始。需要单独运送动物(非配对动物)。所有其他程序都将按规程进行。动物的微观和宏观环境将尽可能保持不变。结论:除了增加可靠性外,其他好处还包括减少动物用量,并有可能降低最终报告的成本和时间。由于减少了因结果可疑而进行重复研究的需要,这项修改后的研究被视为更有效地利用了昂贵的资源。r-EFDT研究设计可以很容易地用于评估兔EFDT和一些一般毒性研究的可重复性。今后需要进行重复研究,以严格评估可重复性以及对研究可靠性的总体影响。
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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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