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重度抑郁症的性别分层全基因组关联荟萃分析。

Sex-stratified genome-wide association meta-analysis of Major Depressive Disorder.

作者信息

Thomas Jodi T, Thorp Jackson G, Huider Floris, Grimes Poppy Z, Wang Rujia, Youssef Pierre, Coleman Jonathan R I, Byrne Enda M, Adams Mark, Medland Sarah E, Hickie Ian B, Olsen Catherine M, Whiteman David C, Whalley Heather C, Penninx Brenda Wjh, van Loo Hanna M, Derks Eske M, Eley Thalia C, Breen Gerome, Boomsma Dorret I, Wray Naomi R, Martin Nicholas G, Mitchell Brittany L

机构信息

Brain and Mental Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

School of Biomedical Sciences, The University of Queensland, Brisbane, Queensland, Australia.

出版信息

medRxiv. 2025 May 6:2025.05.05.25326699. doi: 10.1101/2025.05.05.25326699.

Abstract

There are striking sex differences in the prevalence and symptomology of Major Depressive Disorder (MDD). We conducted the largest sex-stratified genome wide association and genotype-by-sex interaction meta-analyses of MDD to date (Females: 130,471 cases, 159,521 controls. Males: 64,805 cases, 132,185 controls). We found 16 and eight independent genome-wide significant SNPs in females and males, respectively, including one novel variant on the X chromosome. MDD in females and males shows substantial genetic overlap with a large proportion of MDD variants displaying similar effect sizes across sexes. However, we also provide evidence for a higher burden of genetic risk in females which could be due to female-specific variants. Additionally, sex-specific pleiotropic effects may contribute to the higher prevalence of metabolic symptoms in females with MDD. These findings underscore the importance of considering sex-specific genetic architectures in the study of health conditions, including MDD, paving the way for more targeted treatment strategies.

摘要

重度抑郁症(MDD)的患病率和症状学存在显著的性别差异。我们进行了迄今为止最大规模的按性别分层的全基因组关联研究以及MDD的性别与基因型交互作用荟萃分析(女性:130471例病例,159521例对照。男性:64805例病例,132185例对照)。我们分别在女性和男性中发现了16个和8个独立的全基因组显著单核苷酸多态性(SNP),其中包括X染色体上的一个新变体。女性和男性的MDD显示出大量的遗传重叠,很大一部分MDD变体在不同性别中表现出相似的效应大小。然而,我们也提供了证据表明女性的遗传风险负担更高,这可能是由于女性特异性变体所致。此外,性别特异性的多效性效应可能导致患有MDD的女性出现代谢症状的患病率更高。这些发现强调了在包括MDD在内的健康状况研究中考虑性别特异性遗传结构的重要性,为更具针对性的治疗策略铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a76/12083582/4cc72fa19485/nihpp-2025.05.05.25326699v1-f0001.jpg

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