Epidemiology
In a Korean longitudinal study, higher Lp(a) tertiles were associated with lower, not higher, incidence of fatty liver disease (Medicine (Baltimore) 2024)
Original title: Lipoprotein(a) level predicts the development of nonalcoholic fatty liver disease in Korean adults: A retrospective longitudinal study
This retrospective longitudinal study followed 1,501 Korean adults who underwent abdominal ultrasonography at least twice as part of a health checkup program, over a mean 3.36 years. During follow-up, 352 subjects (23.5%) were newly diagnosed with nonalcoholic fatty liver disease (NAFLD). Contrary to expectations, NAFLD incidence decreased as Lp(a) level increased across four Lp(a) groups. After logistic regression adjusting for other risk factors, the odds ratio for developing NAFLD was 0.625 (95% CI 0.440-0.888, P = .032) comparing the highest to the lowest Lp(a) tertile. No significant association was found between Lp(a) and the development of hepatic fibrosis (assessed via the FIB-4 score) among those who developed NAFLD. Lp(a) level is an independent, inverse predictor of incident NAFLD in this Korean cohort, though the authors call for larger studies with longer follow-up to clarify Lp(a)'s effect on both NAFLD development and subsequent fibrosis.
Original abstract
Nonalcoholic fatty liver disease (NAFLD) is a highly prevalent condition in the general population. Although recent studies have demonstrated a link between NAFLD and lipoprotein(a), a low-density lipoprotein-like particle synthesized in the liver, its precise physiological role and mechanism of action remain unclear. This study aimed to investigate the relationship between lipoprotein(a) levels and development of NAFLD and hepatic fibrosis in Korean adults. A total of 1501 subjects who underwent abdominal ultrasonography at least twice as part of a health checkup program were enrolled. Biochemical and ultrasonography results were analyzed longitudinally, and the degree of hepatic fibrosis was calculated in subjects with NAFLD using serum biomarkers, such as fibrosis-4 (FIB-4). During the 3.36-year follow-up period, 352 patients (23.5%) were diagnosed with NAFLD. The subjects were categorized into 4 groups based on their lipoprotein(a) levels. Remarkably, the incidence of NAFLD decreased as the lipoprotein(a) levels increased. Following logistic regression analysis and adjustment for various risk factors, the odds ratio for the development of NAFLD was 0.625 (95% CI 0.440-0.888; P = .032) when comparing the highest to the lowest tertile of lipoprotein(a). However, no significant association was observed between the occurrence of hepatic fibrosis and lipoprotein(a) levels in subjects with NAFLD. Lipoprotein(a) levels have been identified as a significant predictor of NAFLD development. Additional large-scale studies with extended follow-up periods are required to better understand the effect of lipoprotein(a) on NAFLD and hepatic fibrosis.
Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.