TY - JOUR
T1 - Comparative efficacy of pharmacologic therapies for MASH in reducing liver fat content
T2 - Systematic review and network meta-analysis
AU - Koh, Benjamin
AU - Xiao, Jieling
AU - Ng, Cheng Han
AU - Law, Michelle
AU - Gunalan, Shyna Zhuoying
AU - Danpanichkul, Pojsakorn
AU - Ramadoss, Vijay
AU - Loon Sim, Benedix Kuan
AU - Tan, En Ying
AU - Teo, Chong Boon
AU - Nah, Benjamin
AU - Teng, Margaret
AU - Wijarnpreecha, Karn
AU - Seko, Yuya
AU - Lim, Mei Chin
AU - Takahashi, Hirokazu
AU - Nakajima, Atsushi
AU - Noureddin, Mazen
AU - Muthiah, Mark
AU - Huang, Daniel Q.
AU - Loomba, Rohit
N1 - Publisher Copyright:
Copyright © 2024 American Association for the Study of Liver Diseases.
PY - 2024/7/19
Y1 - 2024/7/19
N2 - Background and Aims: Metabolic dysfunction-associated steatohepatitis (MASH) is a leading cause of liver disease. Dynamic changes in magnetic resonance imaging (MRI) proton-density-fat fraction (PDFF) are associated with MASH resolution. We aimed to determine the relative efficacy of therapeutic agents for reducing hepatic fat, assessed by magnetic resonance imaging (MRI) proton-density-fat fraction (PDFF). Approach and results: In this systematic review and network meta-analysis, we searched MEDLINE and Embase from inception until Dec 26, 2023, for published randomized-controlled trials (RCTs) comparing pharmacological interventions in patients with MASH that assessed changes in MRI-PDFF. The primary outcome was the absolute change in MRI-PDFF. The secondary outcome was a ≥30% decline in MRI-PDFF. A surface under-the-curve cumulative ranking probabilities (SUCRA) analysis was performed. Of 1550 records, a total of 39 RCTs (3311 participants) met the inclusion criteria. For MRI-PDFF decline at 24 weeks, aldafermin (SUCRA: 83.65), pegozafermin (SUCRA: 83.46), and pioglitazone (SUCRA: 71.67) were ranked the most effective interventions. At 24-weeks, efinopegdutide (SUCRA: 67.02), semaglutide + firsocostat (SUCRA: 62.43), and pegbelfermin (SUCRA: 61.68) were ranked the most effective interventions for achieving a ≥30% decline in MRI-PDFF. Conclusions: This study provides an updated, relative rank-order efficacy of therapies for MASH in reducing hepatic fat. These data may help inform the design and sample size calculation of future clinical trials and assist selection of combination therapy.
AB - Background and Aims: Metabolic dysfunction-associated steatohepatitis (MASH) is a leading cause of liver disease. Dynamic changes in magnetic resonance imaging (MRI) proton-density-fat fraction (PDFF) are associated with MASH resolution. We aimed to determine the relative efficacy of therapeutic agents for reducing hepatic fat, assessed by magnetic resonance imaging (MRI) proton-density-fat fraction (PDFF). Approach and results: In this systematic review and network meta-analysis, we searched MEDLINE and Embase from inception until Dec 26, 2023, for published randomized-controlled trials (RCTs) comparing pharmacological interventions in patients with MASH that assessed changes in MRI-PDFF. The primary outcome was the absolute change in MRI-PDFF. The secondary outcome was a ≥30% decline in MRI-PDFF. A surface under-the-curve cumulative ranking probabilities (SUCRA) analysis was performed. Of 1550 records, a total of 39 RCTs (3311 participants) met the inclusion criteria. For MRI-PDFF decline at 24 weeks, aldafermin (SUCRA: 83.65), pegozafermin (SUCRA: 83.46), and pioglitazone (SUCRA: 71.67) were ranked the most effective interventions. At 24-weeks, efinopegdutide (SUCRA: 67.02), semaglutide + firsocostat (SUCRA: 62.43), and pegbelfermin (SUCRA: 61.68) were ranked the most effective interventions for achieving a ≥30% decline in MRI-PDFF. Conclusions: This study provides an updated, relative rank-order efficacy of therapies for MASH in reducing hepatic fat. These data may help inform the design and sample size calculation of future clinical trials and assist selection of combination therapy.
KW - Metabolic dysfunction-associated steatohepatitis
KW - Network meta-analysis
KW - Pharmacologic therapies
UR - http://www.scopus.com/inward/record.url?scp=85199531847&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85199531847&partnerID=8YFLogxK
U2 - 10.1097/HEP.0000000000001028
DO - 10.1097/HEP.0000000000001028
M3 - Article
C2 - 39028914
AN - SCOPUS:85199531847
SN - 0270-9139
JO - Hepatology
JF - Hepatology
ER -