Key result
Alcohol-related liver disease is linked to ~16% higher ischemic stroke risk in AF.
Why the study?
The association between distinct steatotic liver disease phenotypes and ischemic stroke risk in patients with atrial fibrillation remains unclear.
Does the presence and phenotype of steatotic liver disease affect the risk of ischemic stroke in patients with atrial fibrillation?
Cohort (n=196,242)
Yes
Does the presence and phenotype of steatotic liver disease affect the risk of ischemic stroke in patients with atrial fibrillation?
Hazard Ratio: 1.16 (95% CI 1.08–1.26)
In patients with atrial fibrillation, alcohol-related steatotic liver disease phenotypes (MetALD and ALD) are associated with an increased risk of ischemic stroke, whereas MASLD alone is not, underscoring the importance of alcohol intake management.
BACKGROUND The updated nomenclature of steatotic liver disease (SLD) recognizes distinct phenotypes, including Metabolic dysfunction-associated steatotic liver disease (MASLD), MASLD with increased alcohol intake (MetALD), and alcohol-related liver disease (ALD). Although cardiovascular risk may differ across SLD phenotypes, their association with stroke risk in patients with atrial fibrillation (AF) remains unclear. OBJECTIVE This study aimed to investigate the association between SLD phenotypes and ischemic stroke risk in AF patients. METHODS AF patients diagnosed between 2010 and 2018 were identified from the Korean health insurance database. According to SLD phenotype, patients were categorized into No-SLD, MASLD, MetALD, and ALD. The primary outcome was ischemic stroke. Subgroup analyses were conducted by CHA2DS2-VA score. RESULTS Among 196,242 patients (No-SLD: 101,308; MASLD: 77,715; MetALD: 8,678; ALD: 8,541), median follow-up was 5.9 years. Compared with No-SLD, MASLD was not associated with stroke risk (adjusted hazard ratio and 95% confidence interval; 1.00, 0.97-1.04), whereas MetALD and ALD were associated with higher risk (1.09, 1.00-1.18 and 1.16, 1.08-1.26, respectively). In exploratory subgroup analyses, the higher risk associated with alcohol-related phenotypes appeared more apparent at lower CHA2DS2-VA scores; however, the 6-year absolute risk differences were approximately 1% or less, and these findings are regarded as hypothesis-generating. CONCLUSION In patients with AF, stroke risk was significantly higher in the alcohol-related SLD phenotypes, MetALD and ALD, whereas MASLD was not associated with stroke risk. These findings are consistent with the current recommendations for comprehensive risk-factor management in AF, with particular attention to alcohol intake in patients with alcohol-related SLD phenotypes.
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Go et al. (2026) conducted a cohort in Atrial fibrillation and steatotic liver disease (n=196,242). Alcohol-related liver disease (ALD) vs. No steatotic liver disease (No-SLD) was evaluated on Ischemic stroke (HR 1.16, 95% CI 1.08-1.26). In patients with atrial fibrillation, alcohol-related liver disease (ALD) was associated with a higher risk of ischemic stroke compared to no steatotic liver disease (HR 1.16; 95% CI 1.08-1.26).
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