MAVMET trial: maraviroc and/or metformin for metabolic dysfunction-associated fatty liver disease(MAFLD) in adults with suppressed HIV

Leanne Mccabe,James E. Burns,Arash Latifoltojar,Frank A. Post,Julie Fox,Erica Pool,Anele Waters, Beatriz Santana,Lucy Garvey,Margaret Johnson, Ian Mcguinness,Manil Chouhan, Jonathan Edwards,Anna L. Goodman,Graham Cooke, Claire Murphy, Yolanda Collaco-Moraes, Helen Webb, Adam Gregory, Fatima Mohamed, Mary Rauchenberger, Stephen D. Ryder, Chris Sandford,Jason V. Baker,Brian Angus,Christoph Boesecke,Chloe Orkin,Shonit Punwani,Andrew Clark,Richard Gilson,David Dunn,Sarah L. Pett

AIDS(2024)

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摘要
Metabolic dysfunction-associated fatty liver disease (MAFLD) is over-represented in people living with HIV (PLWH). Maraviroc (MVC) and/or metformin (MET) may reduce MAFLD by influencing inflammatory pathways and fatty acid metabolism. Open-label, 48-week randomised trial with a 2x2 factorial design. Multicentre HIV clinics. Nondiabetic, virologically-suppressed PLWH, aged ≥35 years, with confirmed/suspected MAFLD (≥1 biochemical/anthropometric/radiological/histological features). Adjunctive MVC; MET; MVC+MET vs. antiretroviral therapy (ART) alone. Change in liver fat fraction (LFF) between baseline and week-48 using Magnetic Resonance Proton Density Fat Fraction (MR PDFF). Six sites enrolled 90 participants (93% male; 81% white; median age 52 [interquartile range, IQR 47–57] years) between 19-Mar-2018 and 11-November-2019. 70% had imaging/biopsy plus ≥1 MAFLD criteria. The analysis included 82/90 with week-0 and -48 scans. Median baseline MR PDFF was 8.9 (4.6–17.1); 40%, 38%, 8%, and 14% had grade zero, one, two, and three steatosis respectively. Mean LFF increased slightly between baseline and follow-up scans: 2.22% MVC, 1.26% MET, 0.81% MVC+MET, and 1.39% ART alone. Prolonged intervention exposure (delayed week-48 scans) exhibited greater increases in MR PDFF (estimated difference 4.23% [95% CI 2.97, 5.48], P < 0.001). There were no differences in predicted change for any intervention compared to ART alone: MVC (−0.42% [95% CI -1.53–0.68, P = 0.45]), MET (-0.62 [-1.81–0.56, P = 0.30]), and MVC+MET (-1.04 [-2.74–0.65, P = 0.23]). Steatosis grade remained unchanged in 55% and increased in 24%. Baseline levels of liver fat were lower than predicted. Contrary to our hypothesis, neither MVC, MET, or the combination significantly reduced MR PDFF compared to ART alone.
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