Shakt Gabrielle, Tsao Noah L, Levin Michael G, Walker Venexia, Kember Rachel L, Klarin Derek, Tsao Phil, Voight Benjamin F, Scali Salvatore T, Damrauer Scott M
Corporal Michael Crescenz VA Medical Center Philadelphia PA USA.
Department of Surgery, Perelman School of Medicine University of Pennsylvania Philadelphia PA USA.
J Am Heart Assoc. 2024 Feb 20;13(4):e030233. doi: 10.1161/JAHA.123.030233. Epub 2024 Feb 16.
Major depressive disorder (MDD) has been identified as a causal risk factor for multiple forms of cardiovascular disease. Although observational evidence has linked MDD to peripheral artery disease (PAD), causal evidence of this relationship is lacking.
Inverse variance weighted 2-sample Mendelian randomization was used to test the association the between genetic liability for MDD and genetic liability for PAD. Genetic liability for MDD was associated with increased genetic liability for PAD (odds ratio [OR], 1.17 [95% CI, 1.06-1.29]; =2.6×10). Genetic liability for MDD was also associated with increased genetically determined lifetime smoking (=0.11 [95% CI, 0.078-0.14]; =1.2×10), decreased alcohol intake (=-0.078 [95% CI, -0.15 to 0]; =0.043), and increased body mass index (=0.10 [95% CI, 0.02-0.19]; =1.8×10), which in turn were associated with genetic liability for PAD (smoking: OR, 2.81 [95% CI, 2.28-3.47], =9.8×10; alcohol: OR, 0.77 [95% CI, 0.66-0.88]; =1.8×10; body mass index: OR, 1.61 [95% CI, 1.52-1.7]; =1.3×10). Controlling for lifetime smoking index, alcohol intake, and body mass index with multivariable Mendelian randomization completely attenuated the association between genetic liability for MDD with genetic liability for PAD.
This work provides evidence for a possible causal association between MDD and PAD that is dependent on intermediate risk factors, adding to the growing body of evidence suggesting that effective management and treatment of cardiovascular diseases may require a composite of physical and mental health interventions.
重度抑郁症(MDD)已被确定为多种心血管疾病的致病风险因素。尽管观察性证据已将MDD与外周动脉疾病(PAD)联系起来,但这种关系的因果证据尚缺乏。
采用逆方差加权两样本孟德尔随机化方法来检验MDD的遗传易感性与PAD的遗传易感性之间的关联。MDD的遗传易感性与PAD的遗传易感性增加相关(优势比[OR],1.17[95%置信区间,1.06 - 1.29];P = 2.6×10)。MDD的遗传易感性还与遗传决定的终生吸烟量增加相关(β = 0.11[95%置信区间,0.078 - 0.14];P = 1.2×10),酒精摄入量减少(β = -0.078[95%置信区间,-0.15至0];P = 0.043),以及体重指数增加(β = 0.10[95%置信区间,0.02 - 0.19];P = 1.8×10),而这些因素又依次与PAD的遗传易感性相关(吸烟:OR,2.81[95%置信区间,2.28 - 3.47],P = 9.8×10;酒精:OR,0.77[95%置信区间,0.66 - 0.88];P = 1.8×10;体重指数:OR,1.61[95%置信区间,1.52 - 1.7];P = 1.3×10)。通过多变量孟德尔随机化控制终生吸烟指数、酒精摄入量和体重指数后,MDD的遗传易感性与PAD的遗传易感性之间的关联完全减弱。
这项研究为MDD与PAD之间可能存在的因果关联提供了证据,这种关联依赖于中间风险因素,这进一步增加了越来越多的证据表明,心血管疾病的有效管理和治疗可能需要综合身心健康干预措施。