Key result
Pemafibrate linked to ~36% lower AST and improved ALT in hypertriglyceridemia and MAFLD.
Why the study?
The therapeutic effect of pemafibrate on metabolic dysfunction-associated fatty liver disease (MAFLD) with hypertriglyceridemia was unknown.
Does pemafibrate improve liver enzymes and lipid profiles in patients with hypertriglyceridemia and MAFLD pathologically diagnosed with NASH?
Observational (n=10)
No
Does pemafibrate improve liver enzymes and lipid profiles in patients with hypertriglyceridemia and MAFLD pathologically diagnosed with NASH?
In a small retrospective cohort, pemafibrate significantly improved liver enzymes and lipid profiles over 6 months in patients with hypertriglyceridemia and biopsy-proven NASH.
May reduce AST/ALT in hypertriglyceridemia with MAFLD; hypothesis-generating, should not yet change practice.
Objective The therapeutic effect of pemafibrate on metabolic dysfunction-associated fatty liver disease (MAFLD) remains unknown. This retrospective, single-arm study investigated the efficacy and safety of pemafibrate in MAFLD patients with hypertriglyceridemia. Methods A total of 10 patients who received pemafibrate (oral, 0.1 mg, twice a day) at Gunma Saiseikai Maebashi Hospital between September 2018 and September 2019 were included. All patients underwent a liver biopsy, and the disease grade and stage were pathologically assessed based on the FLIP algorithm. Results The median age was 66.0 (53.8-74.8) years old, and 5 patients (50.0%) were men. All patients were diagnosed with non-alcoholic steatohepatitis (NASH). The fasting and non-fasting triglyceride (TG) levels were 175 (149-247) mg/dL and 228 (169-335) mg/dL, respectively. The AST and ALT values at 6 months were significantly lower than at baseline [AST: 28.0 (22.0-33.8) U/L vs. 43.5 (24.0-55.0) U/L, p=0.008, ALT: 23.0 (14.8-26.5) U/L vs. 51.5 (23.0-65.3) U/L, p=0.005, respectively], especially in NASH patients with significant activity and advanced fibrosis (p=0.040 and 0.014, respectively). Fasting TG levels were significantly lower and HDL-C levels significantly higher at 6 months than at baseline (p=0.005 and 0.032, respectively). At six months, FIB-4, the aspartate aminotransferase-to-platelet ratio index, and the macrophage galactose-specific lectin-2 binding protein glycosylation isomer level were significantly improved compared with baseline (p=0.041, 0.005 and 0.005, respectively). Treatment-related adverse events were not observed. Conclusion Pemafibrate treatment may be safe and effective for MAFLD patients with hypertriglyceridemia.
No takes yet. Share an insight, caveat, or question.
Hatanaka et al. (2021) conducted an observational in Hypertriglyceridemia and Metabolic Dysfunction-associated Fatty Liver Disease (MAFLD) with Non-alcoholic Steatohepatitis (NASH) (n=10). Pemafibrate vs. Baseline was evaluated on AST level at 6 months (U/L) (p=0.008). Pemafibrate significantly reduced AST and ALT levels at 6 months compared to baseline in patients with hypertriglyceridemia and metabolic dysfunction-associated fatty liver disease.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: