Vanderbilt Genetics Institute, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Division of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Hum Mol Genet. 2021 May 12;30(7):619-628. doi: 10.1093/hmg/ddab068.
Major depressive disorder (MDD) is a common comorbidity in chronic obstructive pulmonary disease (COPD), affecting up to 57% of patients with COPD. Although the comorbidity of COPD and MDD is well established, the causal relationship between these two diseases is unclear. A large-scale electronic health record clinical biobank and genome-wide association study summary statistics for MDD and lung function traits were used to investigate potential shared underlying genetic susceptibility between COPD and MDD. Linkage disequilibrium score regression was used to estimate genetic correlation between phenotypes. Polygenic risk scores (PRS) for MDD and lung function traits were developed and used to perform a phenome-wide association study (PheWAS). Multi-trait-based conditional and joint analysis identified single-nucleotide polymorphisms (SNPs) influencing both lung function and MDD. We found genetic correlations between MDD and all lung function traits were small and not statistically significant. A PRS-MDD was significantly associated with an increased risk of COPD in a PheWAS [odds ratio (OR) = 1.12, 95% confidence interval (CI): 1.09-1.16] when adjusting for age, sex and genetic ancestry, but this relationship became attenuated when controlling for smoking history (OR = 1.08, 95% CI: 1.04-1.13). No significant associations were found between the lung function PRS and MDD. Multi-trait-based conditional and joint analysis identified three SNPs that may contribute to both traits, two of which were previously associated with mood disorders and COPD. Our findings suggest that the observed relationship between COPD and MDD may not be driven by a strong shared genetic architecture.
重度抑郁症(MDD)是慢性阻塞性肺疾病(COPD)的常见合并症,影响多达 57%的 COPD 患者。尽管 COPD 和 MDD 的合并症已得到充分证实,但这两种疾病之间的因果关系尚不清楚。本研究使用了大规模电子健康记录临床生物库和全基因组关联研究 MDD 和肺功能特征汇总统计数据,以调查 COPD 和 MDD 之间潜在的共同遗传易感性。连锁不平衡评分回归用于估计表型之间的遗传相关性。开发了 MDD 和肺功能特征的多基因风险评分(PRS),并用于进行表型全基因组关联研究(PheWAS)。多性状基于条件和联合分析确定了影响肺功能和 MDD 的单核苷酸多态性(SNP)。我们发现 MDD 与所有肺功能特征之间的遗传相关性很小,且无统计学意义。在调整年龄、性别和遗传背景后,PRS-MDD 在 PheWAS 中与 COPD 风险增加显著相关[比值比(OR)=1.12,95%置信区间(CI):1.09-1.16],但在控制吸烟史后,这种相关性减弱(OR=1.08,95%CI:1.04-1.13)。肺功能 PRS 与 MDD 之间未发现显著关联。多性状基于条件和联合分析确定了三个可能与两种性状相关的 SNP,其中两个 SNP 先前与情绪障碍和 COPD 相关。我们的研究结果表明,观察到的 COPD 和 MDD 之间的关系可能不是由强烈的共同遗传结构驱动的。