2026 80th Anniversary
International Convention of PSK

D+12
October 21-23, 2026

Abstracts

P12-9

Risk of major adverse cardiovascular events among young Korean men with metabolic dysfunction-associated steatotic liver disease using causal machine learning

  • Minseol Jang1,2, Miryoung Kim3, Seongmin Yoon1,2, Siin Kim4, Hae Sun Suh*1,2,5
  • 1Department of Regulatory Science, Graduate School, Kyung Hee University
  • 2Institute of Regulatory Innovation through Science, Kyung Hee University
  • 3College of Pharmacy, Sunchon National University
  • 4College of Pharmacy, Kyungsung University
  • 5College of Pharmacy, Kyung Hee University

We aimed to evaluate the association between MASLD and major adverse cardiovascular events (MACE) in young Korean men and explore high-risk population using causal machine learning.

We conducted a nationwide cohort study using linked data from the Military Manpower Administration conscription examination, which includes nearly all Korean men, and the National Health Insurance claims database (2015–2024). MASLD was defined as hepatic steatosis index ≥ 36 with at least one cardiometabolic risk factor, including obesity (BMI ≥23 kg/m2), hypertension (blood pressure ≥ 130/85 mmHg or antihypertensives), diabetes (FPG ≥100 mg/dL or antidiabetics), and dyslipidemia (TG ≥150 mg/dL or lipid-lowering agent) The primary outcome was MACE, defined as myocardial infarction, stroke, heart failure, or cardiovascular death. After 1:1 propensity score matching, Cox PH models were estimated the association between MASLD and MACE. A Causal Survival Forest using 43 covariates was applied to estimate heterogeneous treatment effects. 198,184 MASLD and 1,245,126 non-MASLD male were included. Hazard ratio was 1.33 (95% CI, 1.29-1.41). The CSF estimated an average survival probability difference of -0.0030 (95% CI -0.0042 to -0.0017). Heterogeneous treatment effect was observed in covariates such as history of COPD. MASLD was associated with an increased risk of MACE in young Korean men. Causal machine learning identified clinically relevant high-risk subgroups, supporting targeted prevention strategies.



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