Abstract

BackgroundAtrial electrical and structural remodelling in older individuals with cardiovascular risk factors has been associated with changes in surface electrocardiographic (ECG) parameters (e.g., prolongation of the PR interval) and higher risks of atrial fibrillation (AF). However, it has been difficult to establish whether altered ECG parameters are the cause or a consequence of the myocardial substrate leading to AF. This study aimed to examine the potential causal relevance of ECG parameters on risk of AF using mendelian randomisation (MR).Methods and findingsWeighted genetic scores explaining lifelong differences in P-wave duration, PR interval, and QT interval were constructed, and associations between these ECG scores and risk of AF were estimated among 278,792 UK Biobank participants (mean age: 57 years at recruitment; 19,132 AF cases). The independent genetic variants contributing to each of the separate ECG scores, and their corresponding weights, were based on published genome-wide association studies. In UK Biobank, genetic scores representing a 5 ms longer P-wave duration or PR interval were significantly associated with lower risks of AF (odds ratio [OR] 0.91; 95% confidence interval [CI]: 0.87–0.96, P = 2 × 10−4 and OR 0.94; 95% CI: 0.93–0.96, P = 2 × 10−19, respectively), while longer QT interval was not significantly associated with AF. These effects were independently replicated among a further 17,931 AF cases from the AFGen Consortium. Investigation of potential mechanistic pathways showed that differences in ECG parameters associated with specific ion channel genes had effects on risk of AF consistent with the overall scores, while the overall scores were not associated with changes in left atrial size. Limitations of the study included the inherent assumptions of MR, restriction to individuals of European ancestry, and possible restriction of results to the normal ECG ranges represented in UK Biobank.ConclusionsIn UK Biobank, we observed evidence suggesting a causal relationship between lifelong differences in ECG parameters (particularly PR interval) that reflect longer atrial conduction times and a lower risk of AF. These findings, which appear to be independent of atrial size and concomitant cardiovascular comorbidity, support the relevance of varying mechanisms underpinning AF and indicate that more individualised treatment strategies warrant consideration.

Highlights

  • Atrial fibrillation (AF) is a heterogeneous disease with multiple proposed pathophysiological pathways [1]

  • In UK Biobank, genetic scores representing a 5 ms longer P-wave duration or PR interval were significantly associated with lower risks of AF, while longer QT interval was not significantly associated with AF

  • To explore if our findings applied to supraventricular tachycardia (SVT) phenotypes, which are generally regarded as being mechanistically different to AF [17], we investigated the relationship between the ECG genetic scores and risk of SVT among 2,884 SVT and 275,908 non-SVT cases

Read more

Summary

Introduction

Atrial fibrillation (AF) is a heterogeneous disease with multiple proposed pathophysiological pathways [1]. Simple electrocardiographic (ECG) parameters such as P-wave duration [5,6,7], PR interval [8,9,10], and QT interval [11,12,13,14] have been associated with incident AF in large observational studies, where higher risks of AF were observed at both short and long values (i.e., a “U-shaped relationship”) If causal, these findings may refine our mechanistic understanding of atrial arrhythmias and inform therapeutic strategies. The association between ECG parameters and AF may be subject to reverse causality, since having a history of AF or being treated with rate or rhythm control drugs may alter ECG parameters These potential biases limit the value of observational studies for making causal inferences. This study aimed to examine the potential causal relevance of ECG parameters on risk of AF using mendelian randomisation (MR).

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call