更好的统计报告并不能带来统计上的严谨性:这是二十年来在神经疾病小鼠模型研究中进行的假复制的经验教训。

IF 6.3 1区 医学 Q1 GENETICS & HEREDITY
Constantinos Eleftheriou, Sarah Giachetti, Raven Hickson, Laura Kamnioti-Dumont, Robert Templaar, Alina Aaltonen, Eleni Tsoukala, Nawon Kim, Lysandra Fryer-Petridis, Chloe Henley, Ceren Erdem, Emma Wilson, Beatriz Maio, Jingjing Ye, Jessica C Pierce, Kath Mazur, Lucia Landa-Navarro, Nina G Petrović, Sarah Bendova, Hanan Woods, Manuela Rizzi, Vanesa Salazar-Sanchez, Natasha Anstey, Antonios Asiminas, Shinjini Basu, Sam A Booker, Anjanette Harris, Sam Heyes, Adam Jackson, Alex Crocker-Buque, Aoife C McMahon, Sally M Till, Lasani S Wijetunge, David Ja Wyllie, Catherine M Abbott, Timothy O'Leary, Peter C Kind
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引用次数: 0

摘要

背景:准确确定数据集的样本量(“N”)是实验设计的关键考虑因素。对样本量的错误识别可能导致伪复制,这是一种人为地夸大实验重复次数的过程,这种过程系统性地低估了变异性,高估了效应大小,并使对数据进行的统计测试无效。虽然许多期刊在过去十年中对统计报告采取了严格的要求,但这种努力是否对统计严谨性产生了有意义的影响仍不得而知。方法:在此,我们评估了2001年至2024年间发表的涉及脆性x综合征(FXS)动物模型的神经科学研究和使用神经系统疾病动物模型的研究中这类统计误差的发生率。结果:我们发现大多数出版物中都存在伪复制,尽管在过去十年中统计报告有了显著的改进,但随着时间的推移,伪复制也在增加。这一趋势在2012年至2024年期间从FXS文献推广到神经系统疾病的啮齿动物研究,这表明伪复制仍然是文献中普遍存在的问题。局限性:本研究的范围仅限于神经系统疾病的啮齿动物模型研究,通过允许对单个动物进行重复观察,这些研究有可能被假复制。我们没有考虑实验设计不允许伪复制的综述或文章,例如仅报告行为结果的研究,或未使用推断统计的研究。结论:这些观察结果表明,迫切需要在实验设计中制定更好的标准,并在同行评审中提高对这类错误的警惕。虽然报告标准在过去二十年中有了显著提高,但仅凭这一点还不足以遏制伪复制的盛行。我们提供了如何补救的建议,以及量化这种特定类型统计错误的严重程度。尽管所研究的文献涉及特定的神经科学相关研究领域,但伪复制的含义适用于所有实证研究领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Better statistical reporting does not lead to statistical rigour: lessons from two decades of pseudoreplication in mouse-model studies of neurological disorders.

Background: Accurately determining the sample size ("N") of a dataset is a key consideration for experimental design. Misidentification of sample size can lead to pseudoreplication, a process of artificially inflating the number of experimental replicates which systematically underestimates variability, overestimates effect sizes and invalidates statistical tests performed on the data. While many journals have adopted stringent requirements with regard to statistical reporting over the last decade, it remains unknown whether such efforts have had a meaningful impact on statistical rigour.

Methods: Here, we evaluated the prevalence of this type of statistical error among neuroscience studies involving animal models of Fragile-X Syndrome (FXS) and those using animal models of neurological disorders at large published between 2001 and 2024.

Results: We found that pseudoreplication was present in the majority of publication, increasing over time despite marked improvements in statistical reporting over the last decade. This trend generalised beyond the FXS literature to rodent studies of neurological disorders at large between 2012 and 2024, suggesting that pseudoreplication remains a widespread issue in the literature.

Limitations: The scope of this study was limited to rodent-model studies of neurological disorders which had the potential for being pseudoreplicated, by allowing repeat observations from individual animals. We did not consider reviews or articles whose experimental design could not allow for pseudoreplication, for example studies which reported only behavioural results, or studies which did not use inferential statistics.

Conclusions: These observations identify an urgent need for better standards in experimental design and increased vigilance for this type of error during peer review. While reporting standards have significantly improved over the past two decades, this alone has not been enough to curb the prevalence of pseudoreplication. We offer suggestions for how this can be remedied as well as quantifying the severity of this particular type of statistical error. Although the examined literature concerns a specific neuroscience-related area of research, the implications of pseudoreplication apply to all fields of empirical research.

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来源期刊
Molecular Autism
Molecular Autism GENETICS & HEREDITY-NEUROSCIENCES
CiteScore
12.10
自引率
1.60%
发文量
44
审稿时长
17 weeks
期刊介绍: Molecular Autism is a peer-reviewed, open access journal that publishes high-quality basic, translational and clinical research that has relevance to the etiology, pathobiology, or treatment of autism and related neurodevelopmental conditions. Research that includes integration across levels is encouraged. Molecular Autism publishes empirical studies, reviews, and brief communications.
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