Department of Epidemiology and Biostatistics, Institute of Systems Epidemiology, and West China-PUMC C. C. Chen Institute of Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, China; School of Public Health, Southwest Medical University, Luzhou, Sichuan, China.
Department of Epidemiology and Biostatistics, Institute of Systems Epidemiology, and West China-PUMC C. C. Chen Institute of Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, Sichuan, China.
J Affect Disord. 2024 Mar 1;348:62-69. doi: 10.1016/j.jad.2023.12.028. Epub 2023 Dec 18.
While the association between depression and hypertension has been extensively investigated, the pattern and nature of such association remain inconclusive. We sought to investigate the bidirectional relationship between depression and hypertension and its causal.
We first performed observational analyses using longitudinal data from the UK Biobank. We then performed genetic analyses leveraging summary statistics from large-scale genome-wide association studies (GWASs) conducted in European ancestry for depression and hypertension.
Observational analysis suggested a significant bidirectional phenotypic association between depression and hypertension (Depression → Hypertension: HR = 1.27, 95 % CI: 1.19, 1.36; Hypertension → Depression: HR = 1.65, 95 % CI: 1.58, 1.72). Linkage disequilibrium score regression demonstrated a positive genetic correlation between the two conditions (r=0.15, P = 5.75 × 10). Bidirectional two-sample Mendelian randomization (MR) suggested that genetic liability to depression was significantly associated with an increased risk of hypertension (OR = 1.27, 95 % CI: 1.12, 1.43), while the genetic liability to hypertension was not associated with the risk of depression (OR = 1.01, 95 % CI: 0.99, 1.03). Multivariate MR, after adjusting for smoking, drinking, and body mass index, further supported an independent causal effect of genetic liability to depression on hypertension risk (OR = 1.10, 95 % CI: 1.02, 1.18).
(1) interference of confounders, (2) absence of adequate statistical power, and (3) limitation to European populations.
Our study indicates depression is a causal risk factor for hypertension, whereas the reverse maybe not. Findings support that prevention of depression might help in decreasing hypertension incidence.
尽管抑郁和高血压之间的关联已被广泛研究,但这种关联的模式和性质仍不确定。我们试图探讨抑郁和高血压之间的双向关系及其因果关系。
我们首先使用来自英国生物库的纵向数据进行观察性分析。然后,我们利用针对抑郁和高血压进行的大规模全基因组关联研究(GWAS)的汇总统计数据进行遗传分析。
观察性分析表明,抑郁和高血压之间存在显著的双向表型关联(抑郁→高血压:HR=1.27,95%CI:1.19,1.36;高血压→抑郁:HR=1.65,95%CI:1.58,1.72)。连锁不平衡得分回归表明,两种情况之间存在正的遗传相关性(r=0.15,P=5.75×10)。双向两样本孟德尔随机化(MR)表明,抑郁的遗传易感性与高血压风险增加显著相关(OR=1.27,95%CI:1.12,1.43),而高血压的遗传易感性与抑郁风险无关(OR=1.01,95%CI:0.99,1.03)。调整吸烟、饮酒和体重指数后进行多变量 MR 进一步支持抑郁遗传易感性对高血压风险的独立因果作用(OR=1.10,95%CI:1.02,1.18)。
(1)混杂因素的干扰,(2)缺乏足够的统计能力,(3)仅限于欧洲人群。
我们的研究表明,抑郁是高血压的一个因果危险因素,而反之则不然。研究结果支持预防抑郁可能有助于降低高血压的发病率。