Evidence map›Paper›PMID 39120181›Full record

ArticleHealthcare (Basel, Switzerland)2024

Manifestation and Progression of Metabolic Dysfunction-Associated Steatotic Liver Disease in a Predominately African American Population at a Multi-Specialty Healthcare Organization.

Astha Saini, Brian Rutledge, Anirudh R Damughatla, Mina Rasheed, Paul Naylor, Milton Mutchnick

Abstract read
In one paragraph

Article in Healthcare (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Astha SainiDepartment of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.ORCID 0000-0003-1532-2099
Brian RutledgeDepartment of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.ORCID 0000-0002-4766-909X
Anirudh R DamughatlaDepartment of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.
Mina RasheedDepartment of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.
Paul NaylorDepartment of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.
Milton MutchnickDepartment of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

African Americans (AA) have a high incidence of risk factors associated with MASLD (metabolic dysfunction-associated steatotic liver disease); the AA population has a lower incidence of MASLD and MASH (metabolic-associated steatotic hepatitis) than Caucasian and Hispanic Americans (non-AA). We investigated if underlying risk factor variation between AA and non-AA individuals could provide a rationale for the racial diversity seen in MASLD/MASH. Using ICD-10 codes, patients from 2017 to 2020 with MASLD/MASH were identified and confirmed to have either MASLD or MASH. Despite the large (>80%) AA population in our clinics, only 54% of the MASLD/MASH patients were African American. When the non-invasive NAFLD Fibrosis Scores (NFS) evaluated at early diagnosis were compared to the most recent values, the only increase in fibrosis score by NFS over time was in non-AA MASH patients. The increase in fibrosis only in non-AA MASLD patients is consistent with racial disparity in the disease progression in non-AA as compared to AA patients. Even with the large proportion of AA patients in our study, there was no significant racial disparity in the earliest assessment of either risk factors, laboratory values, or fibrosis scores that would account for racial disparity in the development and progression of MASLD.

Indexed as

MASHMASLDnon-invasive serum markersracial disparity in NASH/NAFLDrisk factors in NASH/NAFLD

Identifiers

PMID39120181
PMCPMC11311600

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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.