Evidence map›Paper›PMID 42100186›Full record

ArticleOpen forum infectious diseases2026

Non-Hispanic Black Persons With HIV Have a Lower Risk of Metabolic Dysfunction-Associated Steatotic Liver Disease and Clinically Significant Fibrosis Compared to Non-Hispanic White and Hispanic Individuals.

Tinsay A Woreta, Samer Gawrieh, Laura A Wilson, Yuchen Xin, Eduardo Vilar-Gomez, Kathleen E Corey, Richard K Sterling, Jordan E Lake, Susanna Naggie, Sonya Heath and 5 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 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

15 authors.

Tinsay A WoretaDivision of Gastroenterology and Hepatology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0001-7292-4518
Samer GawriehDivision of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Laura A WilsonDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0002-6294-4504
Yuchen XinDepartment of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, New York, USA.
Eduardo Vilar-GomezDivision of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Kathleen E CoreyDivision of Gastroenterology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Richard K SterlingDivision of Gastroenterology, Hepatology and Nutrition, Virginia Commonwealth University, Richmond, Virginia, USA.
Jordan E LakeDivision of Infectious Diseases, Department of Medicine, UTHealth, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-0640-5514
Susanna NaggieDivision of Infectious Diseases, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0001-7721-6975
Sonya HeathDivision of Infectious Diseases, University of Alabama, Birmingham, Alabama, USA.ORCID https://orcid.org/0000-0002-3826-0954
Holly CrandallDivision of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.ORCID https://orcid.org/0009-0009-3763-3892
Jennifer C PriceDivision of Gastroenterology and Hepatology, University of California, San Francisco, San Francisco, California, USA.
Rohit LoombaDivision of Gastroenterology and Hepatology, University of California, San Diego, La Jolla, California, USA.
Naga ChalasaniDivision of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Mark S SulkowskiDivision of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0002-2145-6352

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) is a major cause of liver-related morbidity and mortality among people with human immunodeficiency virus (PWH). We aimed to determine the prevalence of MASLD and clinically significant fibrosis among PWH and investigate if racial and ethnic differences exist after adjustment for clinical risk factors and Methods: This cross-sectional analysis included adult PWH prospectively enrolled in 2 US multicenter studies from 2018 to 2023. MASLD was defined as a controlled attenuation parameter (CAP) score ≥263 dB/m with at least 1 cardiometabolic risk factor and clinically significant fibrosis as a liver stiffness measurement ≥8 kPa upon vibration-controlled transient elastography. Multivariable logistic regression analysis was performed to examine the association of race/ethnicity with the presence of MASLD and clinically significant fibrosis, adjusting for clinical risk factors and Results: Of the 996 participants, the mean age was 53.9 years (standard deviation, 12 years) and 72% were male. The prevalence of MASLD and clinically significant fibrosis were 49% and 14%, respectively. Non-Hispanic Black (NHB) persons had the lowest prevalence of MASLD (43%) compared to non-Hispanic White (NHW) (53%) and Hispanic individuals (60%) ( Conclusions: NHB PWH have a lower risk of MASLD and clinically significant fibrosis compared to NHW and Hispanic individuals, even after controlling for clinical risk factors and

Indexed as

HIVliver fibrosisMASLD

Identifiers

PMID42100186
PMCPMC13148014

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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.