Key result
Genetically predicted higher SBP linked to ~2% greater AF risk per mmHg.
Why the study?
Elevated blood pressure is considered the leading risk factor for incident AF, but whether this relationship is causal remains unknown.
Do genetic variants associated with higher blood pressure causally increase the risk of developing atrial fibrillation?
Observational (n=1,000,000)
Mendelian randomization
Yes
Do genetic variants associated with higher blood pressure causally increase the risk of developing atrial fibrillation?
Effect estimate: OR 1.018 (95% CI 1.012-1.024)
p-value: p=< 0.001
Mendelian randomization provides evidence that increased systolic, diastolic, and pulse pressure are causally associated with an increased risk of atrial fibrillation.
Supports causal inference for systolic blood pressure in atrial fibrillation; leaves open whether lowering it prevents incident disease.
AIMS: Observational studies suggest elevated blood pressure (BP) as the leading risk factor for incident atrial fibrillation (AF), but whether this relationship is causal remains unknown. In this study, we used Mendelian randomization (MR) to investigate the potential causal association of BP levels with the risk of developing AF. METHODS AND RESULTS: Genetic variants associated with the BP traits were retrieved from the International Consortium of Blood Pressure-Genome Wide Association Studies (N = 299 024). From 901 reported variants, 894 were assessed in a dedicated Genome-Wide Association Study of AF genetics, including >1 000 000 subjects of European ancestry. We used two-sample MR analyses to examine the potential causal association of systolic BP (SBP) and diastolic BP (DBP) as well as of pulse pressure (PP) with AF. MR analysis identified a potentially causal association between AF and SBP [odds ratio (OR): 1.018 per 1 mmHg increase, 95% confidence interval (CI): 1.012-1.024, P < 0.001], DBP (OR: 1.026, 95% CI: 1.016-1.035, P < 0.001), and PP (OR: 1.014, 95% CI: 1.001-1.028, P = 0.033). These findings were robust in sensitivity analyses, including the MR-Egger method and the MR pleiotropy residual sum and outlier test (MR-PRESSO). The causal relationship of BP and AF did not change when single-nucleotide polymorphisms associated with possible confounders (i.e. coronary artery disease and obesity) of the causal relationship were excluded. CONCLUSIONS: The association between increased BP levels and the risk of AF is likely causal and applies for different BP indices. Independently from other risk factors, optimal BP control might represent an important therapeutic target for AF prevention in the general population.
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Georgiopoulos et al. (2021) conducted an observational in Atrial fibrillation (n=1,000,000). Systolic blood pressure was evaluated on Risk of developing atrial fibrillation (OR 1.018, 95% CI 1.012-1.024, p=< 0.001). Genetically predicted increases in systolic blood pressure were causally associated with an increased risk of atrial fibrillation (OR 1.018 per 1 mmHg increase; 95% CI 1.012-1.024; P<0.001).
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