Key result
High liver fibrosis risk linked to ~78% higher post-AMI all-cause mortality.
Why the study?
Do non-invasive scoring systems for liver fibrosis predict long-term mortality in patients with acute myocardial infarction?
Cohort (n=3,287)
Do non-invasive scoring systems for liver fibrosis predict long-term mortality in patients with acute myocardial infarction?
Non-invasive scoring systems for liver fibrosis, such as FIB-4 and APRI, independently predict long-term mortality in patients following acute myocardial infarction, regardless of diabetes status.
Patients with liver fibrosis and type 2 diabetes mellitus (T2DM) have an increased risk of cardiovascular events. However, long-term prognosis of liver fibrosis and T2DM after acute myocardial infarction (AMI) remain to be investigated. This study compared clinical characteristics and prognosis of AMI patients with T2DM and evidence of liver fibrosis. Patients were stratified into low, intermediate and high-risk for fibrosis, using serum-based non-invasive tests (NITs): Fibrosis-4 Index (FIB-4), Aspartate Aminotransferase to Platelet Ratio Index (APRI) and Non-alcoholic Fatty Liver Disease Fibrosis Score (NFS). The primary outcome was all-cause mortality, Kaplan-Meier curves were constructed for 5-year all-cause mortality. Cox regression analysis was used to determine the independent predictors of mortality, adjusting for confounders. Out of 3287 AMI patients, 1547 were stratified as high-risk by any NIT (mean follow-up duration 2.7 ± 2.3 years). A dose-response relationship was found with increasing mortality risk for higher APRI and NFS scores. High-risk FIB-4 also predicted mortality significantly (adjusted HR [aHR] 1.791, 95% CI 1.436-2.235, p < 0.001). High-risk FIB-4 and APRI independently predicted mortality regardless of T2DM status, while NFS only predicted mortality in T2DM patients. Following AMI, individuals stratified by FIB-4, APRI, NFS as high-risk for liver fibrosis were associated with excess long-term mortality (aHR 1.780, 95% CI 1.442-2.196, p < 0.001). Hence, readily available NITs may be beneficial in risk prognostication of AMI patients.
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Wong et al. (2025) conducted a cohort in Acute myocardial infarction (n=3,287). High risk for liver fibrosis (by FIB-4, APRI, or NFS) vs. Low or intermediate risk for liver fibrosis was evaluated on all-cause mortality (HR 1.780, 95% CI 1.442-2.196, p=< 0.001). High risk for liver fibrosis by non-invasive scores was associated with increased long-term all-cause mortality following acute myocardial infarction (aHR 1.780; 95% CI 1.442-2.196; p<0.001).
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