Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia.
Queensland Brain Institute, University of Queensland, Brisbane, Queensland, Australia.
Nat Genet. 2018 May;50(5):668-681. doi: 10.1038/s41588-018-0090-3. Epub 2018 Apr 26.
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.
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。
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