Evidence map›Paper›PMID 41086163›Full record

ArticlePloS one2025

The association of race with time to severe liver disease diagnoses.

Andrew D Schreiner, Jingwen Zhang, Mulugeta Gebregziabher, Justin Marsden, Patrick D Mauldin, Don C Rockey

Abstract read
In one paragraph

Article in PloS one, 2025. 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.

Andrew D SchreinerDepartment of Medicine, Medical University of South Carolina, Charleston, South Carolina, United States of America.ORCID https://orcid.org/0000-0003-0914-3182
Jingwen ZhangDepartment of Medicine, Medical University of South Carolina, Charleston, South Carolina, United States of America.
Mulugeta GebregziabherDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, United States of America.
Justin MarsdenDepartment of Medicine, Medical University of South Carolina, Charleston, South Carolina, United States of America.
Patrick D MauldinDepartment of Medicine, Medical University of South Carolina, Charleston, South Carolina, United States of America.
Don C RockeyDepartment of Medicine, Medical University of South Carolina, Charleston, South Carolina, United States of America.

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
Proteomics CoreP30DK123704 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RICHARD R. DRAKE · 2020 to 2026
$8.8M
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 P30 DK123704NIDDK NIH HHS R03 DK129558
6 · The paper itself

Abstract

backgroundEvidence suggests that there are racial differences in liver fibrosis progression for patients with chronic liver disease (CLD). We examined the association of Black race with the time to diagnosis of severe liver disease outcomes in primary care patients.

methodsWe captured electronic health record data from a primary care clinic between 2012-2021. Race, categorized as Black and non-Black, was the primary exposure. The outcome was the occurrence of a severe liver event identified by ICD-9/10 codes, defined as a composite of cirrhosis, complications of cirrhosis, hepatocellular carcinoma, and liver transplantation. Cox regression models evaluated the association of Black race with the time to severe liver outcomes while adjusting for potentially confounding covariates.

resultsThe cohort included 20,828 patients of whom 43% identified as Black and 14% had a known diagnosis of CLD during follow-up. Of all patients, 3% received a diagnosis code for a severe liver event. In an unadjusted Cox regression model, Black race was associated with an increased hazard of a severe liver event (HR 1.32; 95%CI 0.98-1.34), but after adjusting for known CLD, baseline fibrosis risk, demographic, and comorbidity variables, Black race was associated with a significantly lower hazard of a severe liver outcome (HR 0.68; 95%CI 0.57-0.81).

conclusionsAfter adjusting for potentially confounding covariates, Black race was associated with a longer time to a severe liver disease diagnosis. This finding raises the possibilities of delayed cirrhosis detection or differences in liver fibrosis progression by racial identifiers.

Indexed as

Liver CirrhosisLiver DiseasesAdultAgedBlack or African AmericanDisease ProgressionFemaleHumansLiver TransplantationMaleMiddle AgedProportional Hazards ModelsSeverity of Illness IndexWhite

Identifiers

PMID41086163
PMCPMC12520358

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.