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Effect of Pemafibrate on the Lipid Profile, Liver Function, and Liver Fibrosis Among Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease.
Hassan, Mona; Al-Obaidi, Hasan; Karrick, Megan; Merza, Nooraldin; Nawras, Yusuf; Saab, Omar; Al-Obaidi, Ahmed Dheyaa; Merza, Fatima; Hashim, Hashim Talib; Al Zubaidi, Khalid; Al-Sabbagh, Daniah; Matbachi, Rand; Noori, Zainab; Amatul-Raheem, Hajra; Mansur, Sarmad; Al Najafi, Omer; Algodi, Marwah; Al Hamdany, Tamarah; Kobeissy, Abdallah.
Affiliation
  • Hassan M; Gastroenterology and Hepatology Department, The University of Toledo, Toledo, OH, USA.
  • Al-Obaidi H; Internal Medicine Department, Jamaica Hospital Medicine Center, Queens, NY, USA.
  • Karrick M; Gastroenterology and Hepatology Department, The University of Toledo, Toledo, OH, USA.
  • Merza N; Gastroenterology and Hepatology Department, The University of Toledo, Toledo, OH, USA.
  • Nawras Y; University of Toledo College of Medicine and Life Science, Toledo, OH, USA.
  • Saab O; Internal Medicine Department, Cleveland Clinic, Cleveland, OH, USA.
  • Al-Obaidi AD; Internal Medicine Department, College of Medicine, University of Baghdad, Baghdad, Iraq.
  • Merza F; Department of Health and Human Services, University of Michigan, Dearborn, MI, USA.
  • Hashim HT; College of Medicine, University of Warith Al-Anbiyaa, Karbala, Iraq.
  • Al Zubaidi K; Internal Medicine Department, University of Al-Mostansiryah College of Medicine, Baghdad, Iraq.
  • Al-Sabbagh D; Internal Medicine Department, Al-Kindy College of Medicine, University of Baghdad, Baghdad, Iraq.
  • Matbachi R; Internal Medicine Department, College of Medicine, University of Baghdad, Baghdad, Iraq.
  • Noori Z; Internal Medicine Department, University of Al-Mostansiryah College of Medicine, Baghdad, Iraq.
  • Amatul-Raheem H; Deccan College of Medical Sciences, Hyderabad, Telangana, India.
  • Mansur S; Gastroenterology and Hepatology Department, The University of Toledo, Toledo, OH, USA.
  • Al Najafi O; Internal Medicine Department, Zucker School of Medicine, Northwell Health at Mather Hospital, Hempstead, NY, USA.
  • Algodi M; Internal Medicine Department, Al-Kindy College of Medicine, University of Baghdad, Baghdad, Iraq.
  • Al Hamdany T; Department of Health and Human Services, University of Michigan, Dearborn, MI, USA.
  • Kobeissy A; Gastroenterology and Hepatology Department, The University of Toledo, Toledo, OH, USA.
Gastroenterology Res ; 17(4): 159-174, 2024 Aug.
Article in En | MEDLINE | ID: mdl-39247710
ABSTRACT

Background:

Metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH) are prevalent conditions linked to obesity and metabolic disturbances, with potential complications such as cirrhosis and cardiovascular risks. This systematic review and meta-analysis aimed to evaluate the efficacy of pemafibrate, a drug targeting fat and sugar metabolism genes, in treating patients with MASLD/MASH.

Methods:

Databases such as MEDLINE, Web of Science, Cochrane Library, and Scopus were searched until September 2023 to identify relevant studies. Selected studies underwent a thorough quality assessment using tools like Risk of Bias 2 tool (ROB-2) and the National Institutes of Health (NIH) Quality Assessment Tools. Comprehensive meta-analysis software was used for statistical evaluations, with a focus on lipid profiles, liver function tests, and fibrosis measurements.

Results:

A total of 13 studies were included; 10 of them were included in the quantitative analysis. Our findings showed that pemafibrate significantly decreased low-density lipoprotein cholesterol (LDL-C) (effect size (ES) = -9.61 mg/dL, 95% confidence interval (CI) -14.15 to -5.08), increased high-density lipoprotein cholesterol (HDL-C) (ES = 3.15 mg/dL, 95% CI 1.53 to 4.78), and reduced triglycerides (TG) (ES = -85.98 mg/dL, 95% CI -96.61 to -75.36). Additionally, pemafibrate showed a marked reduction in liver enzyme levels, including aspartate aminotransferase (AST), alanine aminotransferase (ALT), γ-glutamyl transpeptidase (GGT), and alkaline phosphatase (ALP), with significant effect sizes and P values. For liver stiffness outcomes, pemafibrate decreased AST to platelet ratio index (APRI) (ES = -0.180, 95% CI -0.221 to -0.138).

Conclusions:

Pemafibrate, with its enhanced efficacy and safety profile, presents as a pivotal agent in MASLD/MASH treatment. Its lipid-regulating properties, coupled with its beneficial effects on liver inflammation markers, position it as a potentially invaluable therapeutic option.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Gastroenterology Res Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Canadá

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Gastroenterology Res Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Canadá