Deng Ming-Gang, Chai Chen, Wang Kai, Zhao Zhi-Hui, Nie Jia-Qi, Liu Fang, Liang Yuehui, Liu Jiewei
Department of Psychiatry, Wuhan Mental Health Center, Wuhan 430012, Hubei, China; Department of Psychiatry, Wuhan Hospital for Psychotherapy, Wuhan 430012, Hubei, China.
Emergency Center, Hubei Clinical Research Center for Emergency and Resuscitation, Zhongnan Hospital of Wuhan University, Wuhan 430071, Hubei, China.
Prog Neuropsychopharmacol Biol Psychiatry. 2025 Mar 20;137:111277. doi: 10.1016/j.pnpbp.2025.111277. Epub 2025 Jan 30.
This study aims to investigate the genetic link between mental disorders-depression, schizophrenia (SCZ), and bipolar disorder (BIP)-and abdominal aortic aneurysm (AAA).
We first examined the genetic associations between AAA and mental disorders by analyzing global and local genetic correlations as well as shared genomic loci. Global genetic correlation was assessed using linkage disequilibrium score regression (LDSC) and the GeNetic cOVariance Analyzer (GNOVA), while local genetic correlation was analyzed using the SUPERGNOVA approach. To identify shared genetic variants, the pleiotropy-informed conditional and conjunctional false discovery rate (pleioFDR) method was applied. Subsequently, the univariate Mendelian Randomization (UMR) was employed to evaluate the causal relationship, complemented by multivariate MR (MVMR) to account for potential confounding biases. Additionally, mediation analysis was performed to determine whether known risk factors mediate the identified causal relationships.
Global correlations showed positive links between depression, SCZ, and AAA, but not BIP. Local analyses identified specific genomic regions of correlation. We found 26, 141, and 10 shared loci for AAA with depression, SCZ, and BIP, respectively. UMR indicated significant associations between genetically predicted depression (OR 1.270; 95 % CI 1.071-1.504; p = 0.006) and SCZ (OR 1.047; 95 % CI 1.010-1.084; p = 0.011) with AAA, but not BIP. These results were confirmed by MVMR analyses. Mediation analyses showed that smoking, hypertension, hyperlipidemia, and coronary atherosclerosis mediated the impact of depression on AAA while smoking mediated SCZ's impact.
This study provides evidence that genetically predicted depression and SCZ are linked to an increased risk of AAA, mediated by traditional AAA risk factors.
本研究旨在调查精神障碍(抑郁症、精神分裂症(SCZ)和双相情感障碍(BIP))与腹主动脉瘤(AAA)之间的遗传联系。
我们首先通过分析全局和局部遗传相关性以及共享基因组位点来研究AAA与精神障碍之间的遗传关联。使用连锁不平衡评分回归(LDSC)和遗传协方差分析器(GNOVA)评估全局遗传相关性,而使用SUPERGNOVA方法分析局部遗传相关性。为了识别共享遗传变异,应用了多效性知情条件和联合错误发现率(pleioFDR)方法。随后,采用单变量孟德尔随机化(UMR)评估因果关系,并辅以多变量MR(MVMR)以考虑潜在的混杂偏倚。此外,进行中介分析以确定已知风险因素是否介导已识别的因果关系。
全局相关性显示抑郁症、SCZ与AAA之间存在正相关,但与BIP不存在正相关。局部分析确定了特定的相关基因组区域。我们分别发现AAA与抑郁症、SCZ和BIP的共享位点有26个、141个和10个。UMR表明,遗传预测的抑郁症(OR 1.270;95% CI 1.071 - 1.504;p = 0.006)和SCZ(OR 1.047;95% CI 1.010 - 1.084;p = 0.011)与AAA存在显著关联,但与BIP不存在显著关联。这些结果通过MVMR分析得到证实。中介分析表明,吸烟、高血压、高脂血症和冠状动脉粥样硬化介导了抑郁症对AAA的影响,而吸烟介导了SCZ对AAA的影响。
本研究提供了证据,表明遗传预测的抑郁症和SCZ与AAA风险增加有关,且由传统的AAA风险因素介导。