Evidence map›Paper›PMID 41687818›Full record

ArticleJournal of hepatology2026

Longitudinal changes in cardiometabolic risk factors are associated with changes in liver stiffness in adults with MASLD.

Matthew Dukewich, Laura A Wilson, Jennifer L Dodge, Liyun Yuan, Bilal Hameed, Katherine P Yates, Rohit Loomba, Brent A Neuschwander-Tetri, Wendy Mack, Norah Terrault and 1 more

Abstract read
In one paragraph

Article in Journal of hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. CHAIN Cohort: Prospective Multicenter Study of MASLD With Serial Liver Stiffness Assessments in Cardiovascular Care.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
  3. Article
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

11 authors.

Matthew DukewichDivision of Gastrointestinal and Liver Diseases, University of Southern California, Los Angeles, CA, United States.
Laura A WilsonDepartment of Epidemiology, Johns Hopkins University, Baltimore, MD, United States.
Jennifer L DodgeDivision of Gastrointestinal and Liver Diseases, University of Southern California, Los Angeles, CA, United States; Department of Population and Public Health Sciences, University of Southern California, Los Angeles, CA, United States.
Liyun YuanDivision of Gastrointestinal and Liver Diseases, University of Southern California, Los Angeles, CA, United States.
Bilal HameedDivision of Gastroenterology and Hepatology, University of California, San Francisco, CA, United States.
Katherine P YatesDepartment of Epidemiology, Johns Hopkins University, Baltimore, MD, United States.
Rohit LoombaDivision of Gastroenterology and Hepatology, University of California, San Diego, CA, United States.
Brent A Neuschwander-TetriDivision of Gastroenterology and Hepatology, Saint Louis University, St Louis, MO, United States.
Wendy MackDepartment of Population and Public Health Sciences, University of Southern California, Los Angeles, CA, United States.
Norah TerraultDivision of Gastrointestinal and Liver Diseases, University of Southern California, Los Angeles, CA, United States. Electronic address: terrault@usc.edu.
NASH Clinical Research Network

Funding

Engaging University of California Stakeholders for Biorespository ResearchUL1TR000004 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRANDIS, JENNIFER RUBIN · 2012 to 2015
$78.0M
Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Institute of Translational Health SciencesUL1TR000423 · NCATS · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2012 to 2016
$49.4M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
Pediatric Trials in Non-Alcoholic Steatohepatitis (NASH)U01DK061734 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ROHIT LOOMBA · 2002 to 2026
$24.4M
Continuation of the Non-Alcoholic Steatohepatitis Clinical Research Network (NASHU01DK061730 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI TONASCIA, JAMES A · 2002 to 2018
$23.2M
San Diego Clinical and Translational Research InstituteUL1TR000100 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRESTEIN, GARY S · 2012 to 2015
$19.7M
Research Supplement to Promote Diversity in Health Related ResearchUL1TR002649 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI MOELLER, FREDERICK GERARD · 2018 to 2022
$19.1M
Non Alcoholic Steatohepatitis Clinical Research NetworkU01DK061732 · NIDDK · CLEVELAND CLINIC LERNER COM-CWRU · PI Srinivasan Dasarathy · 2002 to 2026
$12.2M
The Saint Louis University Component of the NASH CRNU01DK061718 · NIDDK · SAINT LOUIS UNIVERSITY · PI BRENT A NEUSCHWANDER-TETRI · 2002 to 2026
$12.0M
VEDS Year2-Continuation of the Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN) Data Coordinating CenterU24DK061730 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI JEANNE M CLARK, David M Shade · 2019 to 2026
$11.3M
Pathogenesis, prognosis, and treatment of NAFLD patientsU01DK061713 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI ANNA MAE ELIZABETH DIEHL · 2002 to 2026
$10.3M
NCATS NIH HHS UL1 TR000004NCATS NIH HHS UL1 TR000006NCATS NIH HHS UL1 TR000100NCATS NIH HHS UL1 TR000423NCATS NIH HHS UL1 TR000436NCATS NIH HHS UL1 TR000439NCATS NIH HHS UL1 TR000448NCATS NIH HHS UL1 TR002649NIDDK NIH HHS T32 DK127977NIDDK NIH HHS U01 DK061713NIDDK NIH HHS U01 DK061718NIDDK NIH HHS U01 DK061728NIDDK NIH HHS U01 DK061730NIDDK NIH HHS U01 DK061732NIDDK NIH HHS U01 DK061734NIDDK NIH HHS U01 DK061737NIDDK NIH HHS U01 DK061738NIDDK NIH HHS U24 DK061730
6 · The paper itself

Abstract

BACKGROUND &

aimsMetabolic dysfunction-associated steatotic liver disease (MASLD) is characterized by cardiometabolic risk factors (CMRFs). Treatment of CMRFs is the cornerstone of MASLD management, yet other than weight loss, the association between changes in CMRFs and changes in liver-related measures is not defined. This study aimed to characterize these longitudinal associations using non-invasive measurements of hepatic fibrosis and steatosis.

methodsAdult participants from the NASH CRN prospective study with biopsy-proven MASLD and at least two sequential vibration-controlled transient elastography (VCTE) exams (≥1 year apart) were included. Annual changes in CMRF parameters were compared against annual changes in liver stiffness measurement (LSM) and controlled attenuation parameter (CAP) using adjusted mixed-effects multinomial logistic regression. The primary outcome was LSM change ≥25% (compared to a reference group of no change, or <25% LSM change), while secondary outcomes were CAP change ≥30% and changes in histologic grading of steatohepatitis or fibrosis.

resultsA total of 1,417 participants were included (mean age 52 years, 38% male, 82% Caucasian). Annual worsening in all CMRFs (except triglycerides and HDL) was associated with LSM worsening (17% greater risk per 1% increase in hemoglobin A1c; 24% greater risk per 5% increase in weight). Improvements in all CMRFs were associated with LSM improvement (32% greater chance per 1% decrease in hemoglobin A1c; 27% greater chance per 5% decrease in weight). Similar associations were observed for changes in CAP.

conclusionsAnnual changes in CMRFs were associated with clinically relevant changes in LSM, CAP, and liver histology. These findings suggest that treatment of metabolic comorbidities is associated with the trajectory of MASLD. IMPACT AND IMPLICATIONS: Guideline-directed treatment of metabolic dysfunction-associated steatotic liver disease (MASLD) is focused on optimal treatment of cardiometabolic comorbidities, but there is limited evidence on the association between outcomes of this treatment and changes in markers of liver health. The results of this study demonstrate that longitudinal changes in these cardiometabolic parameters, particularly those associated with body weight, blood pressure, and glucose intolerance, are associated with both increases and decreases in liver stiffness measurements that represent clinically meaningful changes in liver health. These results are broadly relevant to the care of individuals with MASLD, as these results can provide meaningful treatment targets for guideline development and treating clinicians, as well as provide feasible goals for impacted individuals with MASLD.

Indexed as

Cardiometabolic Risk FactorsFatty LiverLiverLiver CirrhosisNon-alcoholic Fatty Liver DiseaseAdultDisease ProgressionElasticity Imaging TechniquesFemaleHumansLongitudinal StudiesMaleMiddle AgedProspective Studiescardiometabolic risk factorhepatic fibrosislongitudinal analysismetabolic syndromenoninvasive testingvibration-controlled transient elastography

Identifiers

PMID41687818
PMCPMC13613345

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.