School of Public Health, Wuhan University, Wuhan, Hubei Province, China.
Duke Kunshan University, Global Health Research Center, Kunshan, Suzhou, China.
PeerJ. 2024 Mar 15;12:e17073. doi: 10.7717/peerj.17073. eCollection 2024.
Observational studies have demonstrated that a higher resting heart rate (RHR) is associated with an increased risk of dementia. However, it is not clear whether the association is causal. This study aimed to determine the causal effects of higher genetically predicted RHR on the risk of dementia.
We performed a two-sample Mendelian randomization analysis to investigate the causal effect of higher genetically predicted RHR on Alzheimer's disease (AD) using summary statistics from genome-wide association studies. The generalized summary Mendelian randomization (GSMR) analysis was used to analyze the corresponding effects of RHR on following different outcomes: 1) diagnosis of AD (International Genomics of Alzheimer's Project), 2) family history (maternal and paternal) of AD from UK Biobank, 3) combined meta-analysis including these three GWAS results. Further analyses were conducted to determine the possibility of reverse causal association by adjusting for RHR modifying medication.
The results of GSMR showed no significant causal effect of higher genetically predicted RHR on the risk of AD (β = 0.12, = 0.30). GSMR applied to the maternal family history of AD (β = -0.18, = 0.13) and to the paternal family history of AD (β = -0.14, = 0.39) showed the same results. Furthermore, the results were robust after adjusting for RHR modifying drugs (β = -0.03, = 0.72).
Our study did not find any evidence that supports a causal effect of RHR on dementia. Previous observational associations between RHR and dementia are likely attributed to the correlation between RHR and other cardiovascular diseases.
观察性研究表明,静息心率(RHR)较高与痴呆风险增加有关。然而,目前尚不清楚这种关联是否具有因果关系。本研究旨在确定较高的遗传预测 RHR 对痴呆风险的因果影响。
我们使用来自全基因组关联研究的汇总统计数据,进行了两样本孟德尔随机化分析,以调查较高的遗传预测 RHR 对阿尔茨海默病(AD)的因果影响。广义汇总孟德尔随机化(GSMR)分析用于分析 RHR 对以下不同结果的相应影响:1)AD 的诊断(国际阿尔茨海默病基因组学计划),2)来自 UK Biobank 的 AD 的母系和父系家族史,3)包括这三个 GWAS 结果的综合荟萃分析。进一步的分析通过调整 RHR 修饰药物来确定反向因果关联的可能性。
GSMR 的结果表明,较高的遗传预测 RHR 与 AD 的风险之间没有显著的因果关系(β=0.12, = 0.30)。GSMR 应用于 AD 的母系家族史(β=-0.18, = 0.13)和 AD 的父系家族史(β=-0.14, = 0.39)也得出了相同的结果。此外,在调整 RHR 修饰药物后,结果仍然稳健(β=-0.03, = 0.72)。
我们的研究没有发现任何证据支持 RHR 对痴呆症有因果影响。先前 RHR 与痴呆症之间的观察性关联可能归因于 RHR 与其他心血管疾病之间的相关性。