Evidence map›Paper›PMID 38914313›Full record

Trial reportJournal of hepatology2024

Histological improvements following energy restriction and exercise: The role of insulin resistance in resolution of MASH.

Justine M Mucinski, Amadeo F Salvador, Mary P Moore, Talyia M Fordham, Jennifer M Anderson, Grace Shryack, Rory P Cunningham, Guido Lastra, Ayman H Gaballah, Alberto Diaz-Arias and 3 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of hepatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03151798 (Nutrient Overload, Insulin Resistance, and Hepatic Mitochondrial Dysfunction), which is not on this map. Cited by 39 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03151798 nacompletednot on this map

Nutrient Overload, Insulin Resistance, and Hepatic Mitochondrial Dysfunction

TypeinterventionalSponsorUniversity of Missouri-ColumbiaRan2017 to 2023Enrolled336ConditionsNonalcoholic Fatty Liver, Nonalcoholic Steatohepatitis, ObesityArmsPhase II: Lifestyle treatment, Phase II: Control treatment, Phase I: Observational studies
3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
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  17. Sarcopenia and MASLD: novel insights and the future.Nature reviews. Endocrinology · 2026
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Justine M MucinskiDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO 65212, United States.
Amadeo F SalvadorDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO 65212, United States.
Mary P MooreDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO 65212, United States; Research Service, Harry S Truman Memorial Veterans Medical Center, Columbia, MO 65201, United States.
Talyia M FordhamDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO 65212, United States.
Jennifer M AndersonDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO 65212, United States.
Grace ShryackDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO 65212, United States; NextGen Precision Health, Columbia, MO 65201, United States.
Rory P CunninghamDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO 65212, United States; Research Service, Harry S Truman Memorial Veterans Medical Center, Columbia, MO 65201, United States.
Guido LastraEndocrinology and Metabolism, School of Medicine, University of Missouri, Columbia, MO 65212, United States.
Ayman H GaballahDepartment of Radiology, School of Medicine, University of Missouri, Columbia, MO, 65212, United States.
Alberto Diaz-AriasBoyce & Bynum Pathology Laboratories, Columbia, MO, 65201, United States.
Jamal A IbdahDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO 65212, United States; Research Service, Harry S Truman Memorial Veterans Medical Center, Columbia, MO 65201, United States; Department of Medicine, Division of Gastroenterology and Hepatology, School of Medicine, University of Missouri, Columbia, MO 65212, United States; Department of Medical Pharmacology and Physiology, University of Missouri, Columbia, MO, 65212, United States.
R Scott RectorDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO 65212, United States; Research Service, Harry S Truman Memorial Veterans Medical Center, Columbia, MO 65201, United States; NextGen Precision Health, Columbia, MO 65201, United States; Department of Medicine, Division of Gastroenterology and Hepatology, School of Medicine, University of Missouri, Columbia, MO 65212, United States.
Elizabeth J ParksDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO 65212, United States; NextGen Precision Health, Columbia, MO 65201, United States; Department of Medicine, Division of Gastroenterology and Hepatology, School of Medicine, University of Missouri, Columbia, MO 65212, United States. Electronic address: parksej@missouri.edu.

Funding

Nutrient Overload, Insulin Resistance, and Hepatic Mitochondrial DysfunctionR01DK113701 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI IBDAH, JAMAL A, PARKS, ELIZABETH JANE · 2017 to 2021
$3.7M
BLRD VA I01 BX003271BLRD VA I01 BX004710CSRD VA I01 CX002436NIDDK NIH HHS R01 DK113701
6 · The paper itself

Abstract

BACKGROUND &

aimsMetabolic dysfunction-associated steatohepatitis (MASH) is one of the most common liver diseases worldwide and is characterized by multi-tissue insulin resistance. The effects of a 10-month energy restriction and exercise intervention on liver histology, anthropometrics, plasma biochemistries, and insulin sensitivity were compared to standard of care (control) to understand mechanisms that support liver health improvements.

methodsFollowing medical diagnosis of MASH, individuals were randomized to treatment (n = 16) or control (n = 8). Liver fat (magnetic resonance spectroscopy), 18-hour plasma biochemical measurements, and isotopically labeled hyperinsulinemic-euglycemic clamps were completed pre- and post-intervention. Body composition and cardiorespiratory fitness (VO

resultsTreatment induced significant (p <0.05) reductions in body weight, fat mass, and liver injury, while VO

conclusionsExercise and energy restriction elicited significant and clinically meaningful treatment effects on liver health, potentially driven by a redistribution of excess nutrients to skeletal muscle, thereby reducing hepatic nutrient toxicity. Clinical guidelines should emphasize the addition of aerobic exercise in lifestyle treatments for the greatest histologic benefit in individuals with advanced MASH. IMPACT AND IMPLICATIONS: The mechanisms that underpin histologic improvement in individuals with metabolic dysfunction-associated steatohepatitis (MASH) are not well understood. This study evaluated the relationship between liver and metabolic health, testing how changes in one may affect the other. We investigated the effects of energy restriction and exercise on the association between multi-tissue insulin sensitivity and histologic improvements in participants with biopsy-proven MASH. For the first time, these results show that an improvement in peripheral (but not hepatic) insulin sensitivity and systemic markers of muscle function (i.e. cardiorespiratory fitness) were strongly related to resolution of liver disease. Extrahepatic disposal of substrates and improved fitness levels supported histologic improvement, confirming the addition of exercise as crucial to lifestyle interventions in MASH. CLINICAL TRIAL NUMBER: NCT03151798.

Indexed as

Insulin ResistanceAdultBody CompositionCaloric RestrictionExerciseExercise TherapyFatty LiverFemaleHumansLiverMaleMiddle AgedTreatment Outcomeenergy restrictionexercisehistologyinsulin resistancelifestyle treatmentMASHMASLDNAFLD

Identifiers

PMID38914313
PMCPMC12007730

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.