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研究样本的异质性可提高临床前动物研究的可重复性。

Reproducibility of preclinical animal research improves with heterogeneity of study samples.

机构信息

Division of Animal Welfare, VPH Institute, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Centre for Clinical Brain Sciences, Chancellors Building, University of Edinburgh, Edinburgh, United Kingdom.

出版信息

PLoS Biol. 2018 Feb 22;16(2):e2003693. doi: 10.1371/journal.pbio.2003693. eCollection 2018 Feb.

Abstract

Single-laboratory studies conducted under highly standardized conditions are the gold standard in preclinical animal research. Using simulations based on 440 preclinical studies across 13 different interventions in animal models of stroke, myocardial infarction, and breast cancer, we compared the accuracy of effect size estimates between single-laboratory and multi-laboratory study designs. Single-laboratory studies generally failed to predict effect size accurately, and larger sample sizes rendered effect size estimates even less accurate. By contrast, multi-laboratory designs including as few as 2 to 4 laboratories increased coverage probability by up to 42 percentage points without a need for larger sample sizes. These findings demonstrate that within-study standardization is a major cause of poor reproducibility. More representative study samples are required to improve the external validity and reproducibility of preclinical animal research and to prevent wasting animals and resources for inconclusive research.

摘要

在高度标准化条件下进行的单实验室研究是临床前动物研究的金标准。我们使用基于 13 种不同干预措施的 440 项临床前研究的模拟结果,比较了单实验室和多实验室研究设计之间的效果大小估计的准确性。单实验室研究通常无法准确预测效果大小,而更大的样本量会使效果大小估计变得更加不准确。相比之下,包括 2 到 4 个实验室在内的多实验室设计在不增加样本量的情况下,将覆盖率概率提高了多达 42 个百分点。这些发现表明,研究内标准化是导致重现性差的主要原因。需要更具代表性的研究样本,以提高临床前动物研究的外部有效性和重现性,并防止因研究结果不确定而浪费动物和资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c269/5823461/4ff4591bb664/pbio.2003693.g001.jpg

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