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February 19, 2026European Journal of Preventive Cardiology0 citationsOpen Access

Effect of bempedoic acid on cardiovascular risk in patients with metabolic dysfunction-associated steatotic liver disease

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VJVivian de JongSNS E NissenWSWilliam J. Sasiela

Key Points

  • To evaluate the relationship between liver steatosis, fibrosis, and cardiovascular risk, and the effect of bempedoic acid on outcomes related to these conditions.
  • Post-hoc exploratory analysis of CLEAR Outcomes trial with 13,970 patients over 40.6 months
  • Utilized non-invasive tests: Framingham Steatosis Index, Fibrosis-4 index, NAFLD fibrosis score
  • Analyzed time-to-event data using Cox proportional hazards models
  • Liver steatosis was linked to higher incidence of major adverse cardiovascular events (MACE4) in placebo group (HRFSI 1.13)
  • Liver fibrosis also showed increased MACE4 risk (HRFIB4 1.21 and HRNFS 1.16)
  • In patients with liver steatosis, bempedoic acid group had a lower HR for MACE4 (HRFSI_BA 1.04) compared to placebo (HRFSI_PBO 1.14)

Abstract

Abstract Aims Metabolic dysfunction-associated steatotic liver disease (MASLD) encompasses a spectrum of disease starting with liver steatosis and progressing to fibrosis. We evaluated whether non-invasive tests of steatosis and fibrosis are associated with cardiovascular outcomes, and whether bempedoic acid treatment reduced cardiovascular risk. Methods A post-hoc exploratory analysis of CLEAR Outcomes (n=13, 970, median follow-up 40·6 months) was carried out using non-invasive tests to estimate liver steatosis and fibrosis: Framingham Steatosis Index (FSI), Fibrosis-4 index (FIB-4) and NAFLD fibrosis score (NFS). The endpoint was a 4-component major adverse cardiovascular event. Time-to-event was analyzed using Cox proportional hazards models. Results The mean (±SD) age was 66 ±9 years and BMI 30 ±5 kg/m2. Adjusted for other risk factors, liver steatosis was associated with an increased incidence of MACE4 in the placebo group, with hazard ratio (HRFSI) 1·13 (95%CI 1·08–1·18) for 1 unit of FSI increase. Similarly, liver fibrosis was associated with increased risk of MACE4, HRFIB4 1·21 (95%CI 1·09-1·34) and HRNFS 1·16 (95%CI 1·10-1·23) for 1 unit of increase in score. In patients at risk for liver steatosis, the HR for MACE4 associated with 1-unit of FSI increase was lower in the bempedoic acid group: HRFSIBA 1·04 (95%CI 0·99-1·09) vs. HRFSIPBO 1·14 (95%CI 1·09-1·18). Treatment effect was not related to the degree of fibrosis. Conclusion Liver steatosis and fibrosis assessed with non-invasive tests are associated with an increased risk of MACE4. Bempedoic acid reduced MACE4 risk, with an additional benefit in patients with elevated steatosis scores.

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Cite This Study

Jong et al. (2026) studied this question.

synapsesocial.com/papers/6996a768ecb39a600b3ed068https://doi.org/10.1093/eurjpc/zwag102
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