Evidence map›Paper›PMID 42877484›Full record

ArticleLivers2026

The association of cardiovascular disease (CVD) with progression of advanced fibrosis risk in patients with metabolic dysfunction-associated steatotic liver disease (MASLD).

Myra Quiroga, Kathryn P Anderson, Jingwen Zhang, Chloe Bays, Justin Marsden, Andrew D Schreiner

Abstract read
In one paragraph

Article in Livers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Myra QuirogaDepartment of Medicine, Medical University of South Carolina, Charleston, SC, 29425.
Kathryn P AndersonDepartment of Medicine, Medical University of South Carolina, Charleston, SC, 29425.
Jingwen ZhangDepartment of Medicine, Medical University of South Carolina, Charleston, SC, 29425.
Chloe BaysDepartment of Medicine, Medical University of South Carolina, Charleston, SC, 29425.
Justin MarsdenDepartment of Medicine, Medical University of South Carolina, Charleston, SC, 29425.
Andrew D SchreinerDepartment of Medicine, Medical University of South Carolina, Charleston, SC, 29425.

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
Improving the Diagnosis of Liver Disease in Primary Care Patients with Abnormal Liver FunctionK23DK118200 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SCHREINER, ANDREW DAVID · 2018 to 2022
$866k
Improving the Diagnosis and Fibrosis Risk Assessment of Nonalcoholic Fatty Liver Disease in Primary Care Patients with Abnormal Liver ChemistriesR03DK129558 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SCHREINER, ANDREW DAVID · 2022 to 2023
$226k
NCATS NIH HHS UL1 TR001450NIDDK NIH HHS K23 DK118200NIDDK NIH HHS R03 DK129558
6 · The paper itself

Abstract

Objective: Advanced fibrosis is the best predictor of future severe liver outcomes in patients with metabolic dysfunction associated steatotic liver disease (MASLD). Our study aims to determine the association between cardiovascular disease (CVD) with time to a high-risk Fibrosis-4 Index (FIB-4) in patients with low-risk MASLD. Methods: This retrospective cohort study comes from a primary care clinic between 2012 and 2021. The cohort included patients with MASLD and a FIB-4 score at low-risk for advanced fibrosis (<1.3). Patients were followed for the outcome of having a high-risk FIB-4 (≥2.67) or until the end of the study period. The primary predictor variable was CVD, a composite of ICD-9/10 codes for coronary artery, cerebrovascular, and peripheral arterial disease. Covariates included demographic and comorbidity variables. Unadjusted and adjusted Cox regression models were developed for the outcome of time to a high-risk FIB-4 score. Results: The cohort included 859 patients with a mean age of 49.6 years (± 13.7) and mean body mass index of 34.1 (± 8.3) kg/m Conclusion: Our study showed that CVD is associated with an increased risk of progression of FIB-4 scores at low- to high-risk for advanced fibrosis in MASLD patients. Future research investigating how control of cardiometabolic comorbidities impact fibrosis progression in MASLD is warranted.

Indexed as

cardiometabolicFIB-4liver fibrosisMASLD

Identifiers

PMID42877484
PMCPMC13668275

What OpenQuestion holds

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Registered trials

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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.