Department of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Cardiovascular Disease Initiative, The Broad Institute of MIT and Harvard, Cambridge, MA, United States of America.
PLoS One. 2022 May 20;17(5):e0268768. doi: 10.1371/journal.pone.0268768. eCollection 2022.
Both elevated and low resting heart rates are associated with atrial fibrillation (AF), suggesting a U-shaped relationship. However, evidence for a U-shaped causal association between genetically-determined resting heart rate and incident AF is limited. We investigated potential directional changes of the causal association between genetically-determined resting heart rate and incident AF.
Seven cohorts of the AFGen consortium contributed data to this meta-analysis. All participants were of European ancestry with known AF status, genotype information, and a heart rate measurement from a baseline electrocardiogram (ECG). Three strata of instrumental variable-free resting heart rate were used to assess possible non-linear associations between genetically-determined resting heart rate and the logarithm of the incident AF hazard rate: <65; 65-75; and >75 beats per minute (bpm). Mendelian randomization analyses using a weighted resting heart rate polygenic risk score were performed for each stratum. We studied 38,981 individuals (mean age 59±10 years, 54% women) with a mean resting heart rate of 67±11 bpm. During a mean follow-up of 13±5 years, 4,779 (12%) individuals developed AF. A U-shaped association between the resting heart rate and the incident AF-hazard ratio was observed. Genetically-determined resting heart rate was inversely associated with incident AF for instrumental variable-free resting heart rates below 65 bpm (hazard ratio for genetically-determined resting heart rate, 0.96; 95% confidence interval, 0.94-0.99; p = 0.01). Genetically-determined resting heart rate was not associated with incident AF in the other two strata.
For resting heart rates below 65 bpm, our results support an inverse causal association between genetically-determined resting heart rate and incident AF.
静息心率升高和降低均与心房颤动(AF)相关,提示存在 U 型关系。然而,遗传决定的静息心率与 AF 发病之间存在 U 型因果关联的证据有限。我们研究了遗传决定的静息心率与 AF 发病之间因果关联的潜在方向变化。
AFGen 联盟的 7 个队列为这项荟萃分析提供了数据。所有参与者均为欧洲血统,具有已知的 AF 状态、基因型信息和基线心电图(ECG)的心率测量值。使用无工具变量的静息心率三个分层来评估遗传决定的静息心率与事件性 AF 危险率的对数之间可能存在的非线性关联:<65;65-75;和>75 次/分钟(bpm)。对每个分层使用加权静息心率多基因风险评分进行孟德尔随机化分析。我们研究了 38981 名个体(平均年龄 59±10 岁,54%为女性),平均静息心率为 67±11 bpm。在平均 13±5 年的随访期间,4779 名(12%)患者发生了 AF。在观察到的静息心率与事件性 AF 危险比之间存在 U 型关联。在无工具变量的静息心率低于 65 bpm 时,遗传决定的静息心率与事件性 AF 呈负相关(遗传决定的静息心率的危险比为 0.96;95%置信区间为 0.94-0.99;p = 0.01)。在另外两个分层中,遗传决定的静息心率与事件性 AF 无关。
对于静息心率低于 65 bpm,我们的结果支持遗传决定的静息心率与事件性 AF 之间存在负向因果关系。