EQ-5D health utility gains with once-weekly semaglutide 2.4 mg in people with MASH and F2/F3 fibrosis: An analysis of ESSENCE.

JHEP RepAug 11, 2026 (epub)
Clinical ResearchGastroenterologyEndocrinologyOpen access

Margarida Augusto, Robert Bauer, Simon Clancy et al.

✦ AI-curated · Sources linked

In 30 seconds

This exploratory analysis of Week 72 data from the Phase III, randomized, double-blind, placebo-controlled ESSENCE trial assessed mapped EQ-5D health utility in adults with biopsy-confirmed MASH and F2 or F3 fibrosis. Among 800 participants, once-weekly semaglutide 2.4 mg plus standard of care improved utility compared with placebo plus standard of care: the estimated treatment difference was 0.03 (95% CI 0.01-0.06; nominal p = 0.0015). Effects were consistent across fibrosis stages. Utilities were mapped from SF-36 scores, rather than directly measured, and the analysis was exploratory.

Key findings

  • At Week 72, the estimated treatment difference in mapped EQ-5D utility was 0.03 (95% CI 0.01-0.06; nominal p = 0.0015) in favour of semaglutide.
  • The utility improvement was consistent across F2 and F3 fibrosis stages.
  • Baseline mapped EQ-5D utility was approximately 0.78 in both treatment groups.

Why it matters

Health utility estimates can help describe quality-of-life effects in MASH and inform cost-effectiveness evaluations and health technology assessments. The observed improvement adds a preference-based quality-of-life outcome to the trial evidence, although it was derived by mapping SF-36 scores and should not be interpreted as a directly measured EQ-5D change.

What to keep in mind

This was an exploratory analysis using mapped, rather than directly measured, EQ-5D utilities; the source also notes use of a UK-specific tariff.

Source

Published in JHEP Rep. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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