Abstract

Atrial fibrillation (AF) patients have enlarged left atria (LA), but prior studies suggested enlarged atria as both cause and consequence of AF. The aim of this study is to investigate the causal association between AF and LA size and function. In the UK Biobank, all individuals with contoured cardiovascular magnetic resonance data were selected. LA maximal volume (LA max), LA minimal volume (LA min), LA stroke volume and LA ejection fraction were measured and indexed to body surface area (BSA). Two-sample Mendelian randomization analyses were performed using 84 of the known genetic variants associated with AF to assess the association with all LA size and function in individuals without prevalent AF. A total of 4274 individuals (mean age 62.0 ± 7.5 years, 53.2% women) were included. Mendelian randomization analyses estimated a causal effect between genetically determined AF and BSA-indexed LA max, LA min, and LA ejection fraction, but not between AF and LA stroke volume. Leave-one-out analyses showed that the causal associations were attenuated after exclusion of rs67249485, located near PITX2 gene. Our results suggest that AF causally increases LA size and decreases LA ejection fraction. The AF risk allele of rs67249485, located near the PITX2 gene, contributes strongly to these associations.

Highlights

  • Atrial fibrillation (AF) patients have enlarged left atria (LA), but prior studies suggested enlarged atria as both cause and consequence of AF

  • The genetic variants explained more of AF variance than indexed LA maximal volume (LA max) volume (1.7%), indexed LA minimal volume (LA min) volume (1.7%), indexed LA stroke volume (1.8%) and LA ejection fraction (2.0%) (Supplementary Table 3)

  • We took forward the Mendelian randomization approach (MR)-Egger model as primary MR-method to assess the genetic association with indexed LA max and indexed LA stroke volume, whereas we adopted the inverse variance weighted random effects (IVW-RE) model for indexed LA min and LA ejection fraction

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Summary

Introduction

Atrial fibrillation (AF) patients have enlarged left atria (LA), but prior studies suggested enlarged atria as both cause and consequence of AF. Two-sample Mendelian randomization analyses were performed using 84 of the known genetic variants associated with AF to assess the association with all LA size and function in individuals without prevalent AF. Mendelian randomization analyses estimated a causal effect between genetically determined AF and BSA-indexed LA max, LA min, and LA ejection fraction, but not between AF and LA stroke volume. The degree of atrial remodeling can be assessed through measurement of LA volume with cardiovascular magnetic resonance (CMR) i­maging[10]. Co-existence of risk factors of AF and LA size and function makes it difficult to determine causality.

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