Michigan Neuroscience Institute, University of Michigan, Ann Arbor, Michigan.
Department of Biostatistics, School of Public Health, University of Michigan Medicine, Ann Arbor, Michigan; Rogel Cancer Center, University of Michigan Medicine, Ann Arbor, Michigan; Center for Statistical Genetics, School of Public Health, University of Michigan Medicine, Ann Arbor, Michigan.
Biol Psychiatry. 2022 Dec 15;92(12):923-931. doi: 10.1016/j.biopsych.2022.06.004. Epub 2022 Jun 11.
Major depressive disorder (MDD) is a leading cause of disease-associated disability, with much of the increased burden due to psychiatric and medical comorbidity. This comorbidity partly reflects common genetic influences across conditions. Integrating molecular-genetic tools with health records enables tests of association with the broad range of physiological and clinical phenotypes. However, standard phenome-wide association studies analyze associations with individual genetic variants. For polygenic traits such as MDD, aggregate measures of genetic risk may yield greater insight into associations across the clinical phenome.
We tested for associations between a genome-wide polygenic risk score for MDD and medical and psychiatric traits in a phenome-wide association study of 46,782 unrelated, European-ancestry participants from the Michigan Genomics Initiative.
The MDD polygenic risk score was associated with 211 traits from 15 medical and psychiatric disease categories at the phenome-wide significance threshold. After excluding patients with depression, continued associations were observed with respiratory, digestive, neurological, and genitourinary conditions; neoplasms; and mental disorders. Associations with tobacco use disorder, respiratory conditions, and genitourinary conditions persisted after accounting for genetic overlap between depression and other psychiatric traits. Temporal analyses of time-at-first-diagnosis indicated that depression disproportionately preceded chronic pain and substance-related disorders, while asthma disproportionately preceded depression.
The present results can inform the biological links between depression and both mental and systemic diseases. Although MDD polygenic risk scores cannot currently forecast health outcomes with precision at the individual level, as molecular-genetic discoveries for depression increase, these tools may augment risk prediction for medical and psychiatric conditions.
重度抑郁症(MDD)是导致与疾病相关残疾的主要原因,其负担增加的很大一部分原因是精神和医学合并症。这种合并症部分反映了跨疾病的常见遗传影响。将分子遗传工具与健康记录相结合,可以测试与广泛的生理和临床表型的关联。然而,标准的全表型关联研究分析了与个体遗传变异的关联。对于 MDD 等多基因性状,遗传风险的综合衡量可能会更深入地了解跨临床表型的关联。
我们在密歇根基因组倡议的 46782 名无亲缘关系的欧洲血统参与者的全表型关联研究中,测试了 MDD 的全基因组多基因风险评分与医学和精神特征之间的关联。
MDD 多基因风险评分与 15 个医学和精神疾病类别的 211 个特征在全表型显著性阈值上相关。在排除了抑郁症患者后,与呼吸、消化、神经和泌尿生殖系统疾病;肿瘤;和精神障碍仍存在关联。在考虑到抑郁症和其他精神特征之间的遗传重叠后,与吸烟障碍、呼吸状况和泌尿生殖系统状况的关联仍然存在。首次诊断时间的时间分析表明,抑郁症不成比例地先于慢性疼痛和物质相关障碍,而哮喘不成比例地先于抑郁症。
目前的结果可以为抑郁症与精神和系统性疾病之间的生物学联系提供信息。尽管 MDD 多基因风险评分目前无法在个体水平上精确预测健康结果,但随着对抑郁症的分子遗传发现的增加,这些工具可能会增强对医学和精神疾病的风险预测。