Suppr超能文献

失眠的遗传性:一项双胞胎研究的荟萃分析。

The heritability of insomnia: A meta-analysis of twin studies.

机构信息

Sleep and Circadian Neuroscience Institute, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.

Department of Sleep and Cognition, Netherlands Institute for Neuroscience, an Institute of the Royal Netherlands Society for Arts and Sciences, Amsterdam, The Netherlands.

出版信息

Genes Brain Behav. 2021 Apr;20(4):e12717. doi: 10.1111/gbb.12717. Epub 2020 Dec 3.

Abstract

Twin studies of insomnia exhibit heterogeneity in estimates of heritability. This heterogeneity is likely because of sex differences, age of the sample, the reporter and the definition of insomnia. The aim of the present study was to systematically search the literature for twin studies investigating insomnia disorder and insomnia symptoms and to meta-analyse the estimates of heritability derived from these studies to generate an overall estimate of heritability. We further examined whether heritability was moderated by sex, age, reporter and insomnia symptom. A systematic literature search of five online databases was completed on 24 January 2020. Two authors independently screened 5644 abstracts, and 160 complete papers for the inclusion criteria of twin studies from the general population reporting heritability statistics on insomnia or insomnia symptoms, written in English, reporting data from independent studies. We ultimately included 12 papers in the meta-analysis. The meta-analysis focussed on twin intra-class correlations for monozygotic and dizygotic twins. Based on these intra-class correlations, the meta-analytic estimate of heritability was estimated at 40%. Moderator analyses showed stronger heritability in females than males; and for parent-reported insomnia symptoms compared with self-reported insomnia symptoms. There were no other significant moderator effects, although this is likely because of the small number of studies that were comparable across levels of the moderators. Our meta-analysis provides a robust estimate of the heritability of insomnia, which can inform future research aiming to uncover molecular genetic factors involved in insomnia vulnerability.

摘要

同卵双生子和异卵双生子的研究显示,失眠的遗传度估计存在异质性。这种异质性可能是由于性别差异、样本年龄、报告者和失眠的定义不同造成的。本研究旨在系统地搜索文献中关于失眠障碍和失眠症状的双胞胎研究,并对这些研究中得出的遗传度估计进行荟萃分析,以生成遗传度的总体估计。我们进一步研究了遗传度是否受性别、年龄、报告者和失眠症状的调节。我们于 2020 年 1 月 24 日在五个在线数据库中进行了系统的文献搜索。两名作者独立筛选了 5644 篇摘要和 160 篇完整的论文,这些论文来自一般人群的双胞胎研究,报告了失眠或失眠症状的遗传度统计数据,用英文书写,报告了来自独立研究的数据。我们最终将 12 篇论文纳入荟萃分析。荟萃分析集中在同卵双生子和异卵双生子的双胞胎内类相关上。基于这些类内相关,遗传度的荟萃分析估计值为 40%。调节分析显示,女性的遗传度强于男性,与父母报告的失眠症状相比,自我报告的失眠症状的遗传度更强。虽然这可能是由于在调节因素的各个水平上具有可比性的研究数量较少,但没有其他显著的调节效应。我们的荟萃分析为失眠的遗传度提供了一个可靠的估计,这可以为旨在揭示与失眠易感性相关的分子遗传因素的未来研究提供信息。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验