Department of Geriatric Medicine, Center of Coronary Circulation, Xiangya Hospital, Central South University, Changsha, China; Department of Geriatric Disease, National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China; Department of Cardiovascular Medicine, Xiangya Hospital, Central South University, Changsha, China.
Department of Geriatric Medicine, Center of Coronary Circulation, Xiangya Hospital, Central South University, Changsha, China; Department of Geriatric Disease, National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.
J Am Med Dir Assoc. 2024 Mar;25(3):506-513.e29. doi: 10.1016/j.jamda.2023.10.009. Epub 2023 Nov 17.
Although observational studies have reported the association between frailty and mental disorders, the causality remains unclear. We aimed to evaluate the bidirectional causal association between frailty levels and mental disorders using a 2-sample Mendelian randomization (MR) analysis.
A bidirectional, 2-sample Mendelian randomization (MR) analysis.
Instrumental variables were obtained from large-scale genome-wide association study (GWAS) of a European-descent population for frailty index (FI, n = 175,226), Fried Frailty Score (FFS, n = 386,565), major depressive disorder (MDD, n = 674,452), bipolar disorder (n = 353,899), anxiety and stress-related disorder (ASRD, n = 31,880), and schizophrenia (n = 127,906).
Two-sample MR analyses were conducted using inverse variance-weighted method, with sensitivity analyses using MR-Egger, weighted median, and simple median methods.
Per SD increase in genetically predicted FI and FFS increased the risk of MDD [odds ratio (OR) 1.56, 95% CI 1.27-1.94, P = 3.65 × 10, and OR 1.67, 95% CI 1.26-2.20, P = 3.02 × 10, respectively]. Per-SD increase in genetically predicted FI also increased the risk of ASRD (OR 2.76, 95% CI 1.36-5.60, P = .005). No significant effect was observed for frailty levels on the risk of bipolar disorder and schizophrenia. In the reverse direction, genetically predicted MDD was associated with higher FI (β 0.182, 95% CI 0.087-0.277, P = 1.79 × 10) and FFS (β 0.121, 95% CI 0.087-0.155, P = 4.43 × 10). No reliable evidence supported the effects of genetically predicted bipolar disorder, ASRD, or schizophrenia on frailty levels.
A bidirectionally causal association exists between frailty levels and MDD, and higher FI is associated with a higher risk of ASRD. No reliable evidence suggested the causal associations of other mental disorders with frailty. Our findings provided evidence for introduction of psychological-related strategies in management of frailty.
尽管观察性研究报告了衰弱与精神障碍之间的关联,但因果关系仍不清楚。我们旨在使用两样本孟德尔随机化(MR)分析来评估衰弱水平与精神障碍之间的双向因果关系。
双向、两样本孟德尔随机化(MR)分析。
工具变量来自欧洲裔人群的大规模全基因组关联研究,用于衰弱指数(FI,n=175226)、弗里德衰弱评分(FFS,n=386565)、重度抑郁症(MDD,n=674452)、双相情感障碍(n=353899)、焦虑和应激相关障碍(ASRD,n=31880)和精神分裂症(n=127906)。
使用逆方差加权法进行两样本 MR 分析,并使用 MR-Egger、加权中位数和简单中位数方法进行敏感性分析。
遗传预测 FI 和 FFS 每增加一个标准差,患 MDD 的风险就会增加[比值比(OR)1.56,95%置信区间(CI)1.27-1.94,P=3.65×10,OR 1.67,95%CI 1.26-2.20,P=3.02×10]。遗传预测 FI 的每增加一个标准差也会增加 ASRD 的风险(OR 2.76,95%CI 1.36-5.60,P=0.005)。衰弱水平与双相情感障碍和精神分裂症的风险之间没有观察到显著的影响。在相反的方向上,遗传预测的 MDD 与更高的 FI(β0.182,95%CI 0.087-0.277,P=1.79×10)和 FFS(β0.121,95%CI 0.087-0.155,P=4.43×10)相关。没有可靠的证据支持遗传预测的双相情感障碍、ASRD 或精神分裂症与衰弱水平之间的因果关系。
衰弱水平与 MDD 之间存在双向因果关系,较高的 FI 与 ASRD 的风险增加有关。没有可靠的证据表明其他精神障碍与衰弱之间存在因果关系。我们的研究结果为在衰弱管理中引入心理相关策略提供了证据。