Effects of Pemafibrate on LDL-C and Related Lipid Markers in Patients with MASLD: A Sub-Analysis of the PEMA-FL Study.

Ryohei Tanigawa, Hideki Suganami, Hirokazu Takahashi, Yuki Iida, Yuichiro Eguchi, Atsushi Nakajima, Shizuya Yamashita, Rohit Loomba, Ayumi Saito, Masaya Tanahashi

Journal: Journal of atherosclerosis and thrombosis 2025;32(7):823-839

PMID: 39694503

Abstract

AIM

In the PEMA-FL study in patients with metabolic dysfunction-associated steatotic liver disease (MASLD), pemafibrate was shown to significantly decrease low-density lipoprotein cholesterol (LDL-C) levels. We aimed to investigate the mechanisms of pemafibrate-induced LDL-C reduction in patients with MASLD by conducting an additional sub-analysis of the PEMA-FL study.

METHODS

The PEMA-FL study randomized 118 patients with MASLD to receive pemafibrate or placebo for 72 weeks. This sub-analysis examined the percentage change in LDL-C and related lipid markers by tertile of baseline LDL-C levels and the correlation between these changes in the pemafibrate group.

RESULTS

Pemafibrate significantly decreased LDL-C levels approximately 25% (p<0.001 at all timepoints) from baseline in the highest tertile of baseline LDL-C levels (≥ 137.5 mg/dL), with similar trends for non-high-density lipoprotein cholesterol (non-HDL-C) and apolipoprotein B (ApoB) levels. Lipoprotein (a) [Lp(a)] levels decreased only in patients with the highest baseline LDL-C levels. Regardless of the baseline LDL-C levels, pemafibrate altered the LDL particle profile (increased LDL particle size and decreased the number); reduced lathosterol, β-sitosterol, and campesterol; and increased angiopoietin-like protein 3 (ANGPTL3). The percentage change in LDL-C positively correlated with that in ApoB, non-HDL-C, Lp(a), lathosterol, β-sitosterol, and campesterol but not HDL-C and ANGPTL3.

CONCLUSION

Pemafibrate reduced LDL-C, ApoB, and non-HDL-C levels in patients with MASLD, and the effect was greater in those with higher baseline LDL-C levels. Pemafibrate may clinically benefit patients with MASLD by improving LDL-C levels and the LDL particle profile.

Address: Global Clinical Development Department, Kowa Company Ltd.; Liver Center, Saga University Hospital.; Department of Gastroenterology and Hepatology, Yokohama City University Graduate School of Medicine.; Loco Medical General Institute.; Liver Center, Saga University Hospital.; MASLD Research Center, Division of Gastroenterology and Hepatology, Department of Medicine, University of California San Diego.; Clinical Data Science Department, Kowa Company Ltd.; Global Clinical Development Department, Kowa Company Ltd.; Department of Cardiology, Rinku General Medical Center.
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