Suppr超能文献

动物实验的授权基于信任而非科学严谨性的证据。

Authorization of Animal Experiments Is Based on Confidence Rather than Evidence of Scientific Rigor.

作者信息

Vogt Lucile, Reichlin Thomas S, Nathues Christina, Würbel Hanno

机构信息

Division of Animal Welfare, Veterinary Public Health Institute, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Division of VPH-Epidemiology, Veterinary Public Health Institute, Vetsuisse Faculty, University of Bern, Liebefeld, Switzerland.

出版信息

PLoS Biol. 2016 Dec 2;14(12):e2000598. doi: 10.1371/journal.pbio.2000598. eCollection 2016 Dec.

Abstract

Accumulating evidence indicates high risk of bias in preclinical animal research, questioning the scientific validity and reproducibility of published research findings. Systematic reviews found low rates of reporting of measures against risks of bias in the published literature (e.g., randomization, blinding, sample size calculation) and a correlation between low reporting rates and inflated treatment effects. That most animal research undergoes peer review or ethical review would offer the possibility to detect risks of bias at an earlier stage, before the research has been conducted. For example, in Switzerland, animal experiments are licensed based on a detailed description of the study protocol and a harm-benefit analysis. We therefore screened applications for animal experiments submitted to Swiss authorities (n = 1,277) for the rates at which the use of seven basic measures against bias (allocation concealment, blinding, randomization, sample size calculation, inclusion/exclusion criteria, primary outcome variable, and statistical analysis plan) were described and compared them with the reporting rates of the same measures in a representative sub-sample of publications (n = 50) resulting from studies described in these applications. Measures against bias were described at very low rates, ranging on average from 2.4% for statistical analysis plan to 19% for primary outcome variable in applications for animal experiments, and from 0.0% for sample size calculation to 34% for statistical analysis plan in publications from these experiments. Calculating an internal validity score (IVS) based on the proportion of the seven measures against bias, we found a weak positive correlation between the IVS of applications and that of publications (Spearman's rho = 0.34, p = 0.014), indicating that the rates of description of these measures in applications partly predict their rates of reporting in publications. These results indicate that the authorities licensing animal experiments are lacking important information about experimental conduct that determines the scientific validity of the findings, which may be critical for the weight attributed to the benefit of the research in the harm-benefit analysis. Similar to manuscripts getting accepted for publication despite poor reporting of measures against bias, applications for animal experiments may often be approved based on implicit confidence rather than explicit evidence of scientific rigor. Our findings shed serious doubt on the current authorization procedure for animal experiments, as well as the peer-review process for scientific publications, which in the long run may undermine the credibility of research. Developing existing authorization procedures that are already in place in many countries towards a preregistration system for animal research is one promising way to reform the system. This would not only benefit the scientific validity of findings from animal experiments but also help to avoid unnecessary harm to animals for inconclusive research.

摘要

越来越多的证据表明临床前动物研究存在高偏倚风险,这对已发表研究结果的科学有效性和可重复性提出了质疑。系统评价发现,已发表文献中针对偏倚风险的措施报告率较低(例如随机化、盲法、样本量计算),且报告率低与夸大的治疗效果之间存在相关性。大多数动物研究都经过同行评审或伦理审查,这将有可能在研究进行之前的早期阶段发现偏倚风险。例如,在瑞士,动物实验是根据详细的研究方案描述和危害-效益分析来发放许可的。因此,我们筛选了提交给瑞士当局的动物实验申请(n = 1277),以了解针对七种基本偏倚防范措施(分配隐藏、盲法、随机化、样本量计算、纳入/排除标准、主要结局变量和统计分析计划)的使用描述率,并将其与这些申请中所描述研究的代表性出版物子样本(n = 50)中相同措施的报告率进行比较。在动物实验申请中,针对偏倚的措施描述率极低,平均从统计分析计划的2.4%到主要结局变量的19%不等;而在这些实验的出版物中,样本量计算的描述率为0.0%,统计分析计划的描述率为34%。基于七种偏倚防范措施的比例计算内部效度评分(IVS),我们发现申请的IVS与出版物的IVS之间存在微弱的正相关(斯皮尔曼rho系数 = 0.34,p = 0.014),这表明这些措施在申请中的描述率部分预示了它们在出版物中的报告率。这些结果表明,发放动物实验许可的当局缺乏有关实验实施的重要信息,而这些信息决定了研究结果的科学有效性,这对于危害-效益分析中赋予研究益处的权重可能至关重要。类似于尽管针对偏倚的措施报告不佳但仍被接受发表的手稿,动物实验申请可能常常基于隐含的信心而非科学严谨性的明确证据而获得批准。我们的研究结果对当前动物实验的授权程序以及科学出版物的同行评审过程提出了严重质疑,从长远来看,这可能会损害研究的可信度。在许多国家现有的授权程序基础上,发展出一种动物研究预注册系统是改革该系统的一种有前景的方式。这不仅将有利于动物实验结果的科学有效性,还将有助于避免因无定论的研究而对动物造成不必要的伤害。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d465/5135031/03377e63f460/pbio.2000598.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验