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作为神经发育疾病模型的转基因动物:系统评价报告质量综述

Genetically modified animals as models of neurodevelopmental conditions: A review of systematic review reporting quality.

作者信息

Wilson Emma, Currie Gillian, Macleod Malcolm, Kind Peter, Sena Emily S

机构信息

Centre for Clinical Brain Sciences, The University of Edinburgh, Edinburgh, UK.

Simons Initiative for the Developing Brain, The University of Edinburgh, Edinburgh, UK.

出版信息

Brain Neurosci Adv. 2024 Oct 18;8:23982128241287279. doi: 10.1177/23982128241287279. eCollection 2024 Jan-Dec.

Abstract

Using genetically modified animals to model neurodevelopmental conditions helps better our understanding of biology underlying these conditions. Animal research has unique characteristics not shared with clinical research, meaning systematic review methods must be adapted to this context. We aim to evaluate the quantity, characteristics, and reporting quality of systematic reviews which synthesise research using genetically modified animals to model neurodevelopmental conditions. On 23 January 2023, we searched PubMed, Embase, and the Web of Science Core Collection to identify systematic reviews of genetic neurodevelopmental condition animal research where the modified gene was one in a list of 102 genes associated with neurodevelopmental conditions identified through large-scale exome sequencing or , , or . Two independent reviewers screened studies based on full text and assessed the reporting quality of relevant reviews using an adapted version of the PRISMA checklist (PRISMA-Pre). Twelve review publications met our criteria. We found mixed levels of reporting: items such as identifying the publication as a systematic review in the title, search strategies, and funding sources being well reported, and others such as protocol registration and data sharing less well reported. We also identified 19 review registrations via PROSPERO, most of which remain unpublished after their anticipated end dates. Systematic reviews are limited by lack of reporting. Increased awareness of reporting guidelines may help authors increase the transparency and reproducibility, and therefore the reliability, of their systematic reviews.

摘要

使用转基因动物来模拟神经发育疾病有助于加深我们对这些疾病背后生物学机制的理解。动物研究具有一些临床研究所没有的独特特征,这意味着系统评价方法必须适用于此背景。我们旨在评估使用转基因动物模拟神经发育疾病的系统评价的数量、特征和报告质量。2023年1月23日,我们检索了PubMed、Embase和科学网核心合集,以识别对基因神经发育疾病动物研究的系统评价,其中修饰基因是通过大规模外显子组测序确定的与神经发育疾病相关的102个基因列表中的一个,或者 , ,或者 。两名独立评审员根据全文筛选研究,并使用PRISMA清单(PRISMA-Pre)的改编版本评估相关评价的报告质量。12篇综述出版物符合我们的标准。我们发现报告水平参差不齐:诸如在标题中识别该出版物为系统评价、检索策略和资金来源等项目报告良好,而诸如方案注册和数据共享等其他项目报告较差。我们还通过PROSPERO识别了19项综述注册,其中大多数在预期结束日期后仍未发表。系统评价受到报告不足的限制。提高对报告指南的认识可能有助于作者提高其系统评价的透明度、可重复性,从而提高其可靠性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71bc/11489925/6922d418e473/10.1177_23982128241287279-fig1.jpg

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