文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

全基因组关联分析确定了 44 个风险变异,并完善了重度抑郁症的遗传结构。

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.

机构信息

Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia.

Queensland Brain Institute, University of Queensland, Brisbane, Queensland, Australia.

出版信息

Nat Genet. 2018 May;50(5):668-681. doi: 10.1038/s41588-018-0090-3. Epub 2018 Apr 26.


DOI:10.1038/s41588-018-0090-3
PMID:29700475
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5934326/
Abstract

Major depressive disorder (MDD) is a common illness accompanied by considerable morbidity, mortality, costs, and heightened risk of suicide. We conducted a genome-wide association meta-analysis based in 135,458 cases and 344,901 controls and identified 44 independent and significant loci. The genetic findings were associated with clinical features of major depression and implicated brain regions exhibiting anatomical differences in cases. Targets of antidepressant medications and genes involved in gene splicing were enriched for smaller association signal. We found important relationships of genetic risk for major depression with educational attainment, body mass, and schizophrenia: lower educational attainment and higher body mass were putatively causal, whereas major depression and schizophrenia reflected a partly shared biological etiology. All humans carry lesser or greater numbers of genetic risk factors for major depression. These findings help refine the basis of major depression and imply that a continuous measure of risk underlies the clinical phenotype.

摘要

重度抑郁症(MDD)是一种常见疾病,伴随着相当高的发病率、死亡率、成本和自杀风险。我们进行了一项全基因组关联荟萃分析,基于 135458 例病例和 344901 例对照,确定了 44 个独立且显著的位点。遗传发现与重度抑郁症的临床特征有关,并提示病例中大脑区域存在解剖差异。抗抑郁药物的靶点和参与基因剪接的基因与较小的关联信号富集。我们发现,重度抑郁症的遗传风险与受教育程度、体重和精神分裂症之间存在重要关系:受教育程度较低和体重较高被认为是因果关系,而重度抑郁症和精神分裂症反映了部分共同的生物学病因。所有人类都或多或少地携带了重度抑郁症的遗传风险因素。这些发现有助于细化重度抑郁症的基础,并暗示临床表型的基础是连续的风险测量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c9a/5934326/e0ad21ea11c2/nihms943355f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c9a/5934326/f9302c14e002/nihms943355f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c9a/5934326/cad5eea44132/nihms943355f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c9a/5934326/dc0df39346eb/nihms943355f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c9a/5934326/e0ad21ea11c2/nihms943355f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c9a/5934326/f9302c14e002/nihms943355f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c9a/5934326/cad5eea44132/nihms943355f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c9a/5934326/dc0df39346eb/nihms943355f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c9a/5934326/e0ad21ea11c2/nihms943355f4.jpg

相似文献

[1]
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.

Nat Genet. 2018-4-26

[2]
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.

Biol Psychiatry. 2017-2-15

[3]
Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression.

Mol Psychiatry. 2020-7

[4]
Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools.

Brain. 2022-3-29

[5]
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder.

JAMA Psychiatry. 2015-7

[6]
GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

Am J Psychiatry. 2019-6-5

[7]
Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study.

Am J Med Genet B Neuropsychiatr Genet. 2014-6-25

[8]
Dissection of major depressive disorder using polygenic risk scores for schizophrenia in two independent cohorts.

Transl Psychiatry. 2016-11-1

[9]
Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors.

Mol Psychiatry. 2012-3-27

[10]
Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank.

Transl Psychiatry. 2018-1-10

引用本文的文献

[1]
Polygenic scores for psychiatric traits mediate the impact of multigenerational history for depression on offspring psychopathology.

Mol Psychiatry. 2025-9-8

[2]
Genetic susceptibility to depressive symptoms in middle-aged to older Americans: time-varying effects and effect modification by early psychosocial factors.

Soc Psychiatry Psychiatr Epidemiol. 2025-8-30

[3]
Spousal correlations for nine psychiatric disorders are consistent across cultures and persistent over generations.

Nat Hum Behav. 2025-8-28

[4]
Sex-stratified genome-wide association meta-analysis of major depressive disorder.

Nat Commun. 2025-8-26

[5]
A common neural signature between genetic and environmental risk for mental illness.

Transl Psychiatry. 2025-8-21

[6]
Polygenic scores for depression are associated with indices of neighborhood adversity.

J Psychopathol Clin Sci. 2025-8-21

[7]
Association between polygenic risk for Major Depression and brain structure in a mega-analysis of 50,975 participants across 11 studies.

Mol Psychiatry. 2025-8-19

[8]
Interplay Between Depression and Inflammatory Bowel Disease: Shared Pathogenetic Mechanisms and Reciprocal Therapeutic Impacts-A Comprehensive Review.

J Clin Med. 2025-8-5

[9]
Investigating the genetic relationship of intracranial and subcortical brain volumes with depression and other psychiatric disorders.

Imaging Neurosci (Camb). 2024-9-19

[10]
Polygenic Risk Scores for Pediatric Obsessive-Compulsive Symptoms and their Mediating Effect in Clinically Diagnosed Samples of Obsessive-Compulsive Disorder, Attention-Deficit/Hyperactivity Disorder, Anxiety, Depression, Autism and Tourette syndrome.

Res Sq. 2025-8-6

本文引用的文献

[1]
Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia.

Nat Commun. 2018-8-7

[2]
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.

Nat Genet. 2018-4-9

[3]
Causal associations between risk factors and common diseases inferred from GWAS summary data.

Nat Commun. 2018-1-15

[4]
Psychiatric Genomics: An Update and an Agenda.

Am J Psychiatry. 2018-1-1

[5]
The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.

Mol Psychiatry. 2017-9-19

[6]
An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome.

Nat Neurosci. 2017-10

[7]
HUGIn: Hi-C Unifying Genomic Interrogator.

Bioinformatics. 2017-12-1

[8]
Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence.

Nat Genet. 2017-7

[9]
Pleiotropic Effects of Trait-Associated Genetic Variation on DNA Methylation: Utility for Refining GWAS Loci.

Am J Hum Genet. 2017-6-1

[10]
Conditional eQTL analysis reveals allelic heterogeneity of gene expression.

Hum Mol Genet. 2017-4-15

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

推荐工具

医学文档翻译智能文献检索