Evidence map›Paper›PMID 40498739›Full record

ArticlePloS one2025

Longitudinal effect of HCV cure on markers of kidney disease.

Javier Cepeda, Mohamed Atta, Katie Zook, Miles Landry, Paula Maier, George Schwartz, Gregory Lucas

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

7 authors.

Javier CepedaDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.ORCID https://orcid.org/0000-0003-0304-3172
Mohamed AttaDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Katie ZookDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Miles LandryDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Paula MaierDepartment of Pediatrics, University of Rochester Medical Center, Rochester, New York, United States of America.
George SchwartzDepartment of Pediatrics, University of Rochester Medical Center, Rochester, New York, United States of America.
Gregory LucasDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.ORCID https://orcid.org/0000-0002-3013-4339

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic hepatitis C infection has been linked to chronic kidney disease. Despite availability of all oral highly curative direct acting antiviral treatment for more than a decade, impact of HCV cure on extrinsically measured iohexol glomerular filtration rate (iGFR), a marker of kidney function, has not been rigorously evaluated. Over two recruitment periods (October 14, 2010 - July 23, 2012 and December 15, 2015 - September 12, 2019), we enrolled 208 participants with chronic HCV infection, 63% of whom were co-infected with HIV. We conducted linear mixed effects modeling to evaluate the change in iGFR slope among participants who were and were not cured from chronic HCV. Secondary outcomes included albuminuria (urine albumin-creatinine-ratio ≥30 mg/g). At baseline, the median age was 51 years (interquartile range: 47-56), most of whom were Black (85%), and male (71%). In the multivariable-adjusted model, including baseline iGFR and other covariates, the adjust difference in iGFR slope was 2.37 mL/min/1.73 m2 per year (95% CI: 0.72, 4.03, p = 0.0051) higher among HCV treated participants compared to untreated. HCV treatment status was not associated with probability of albuminuria. Among participants chronically infected with HCV, we identified a significant positive impact of HCV cure on kidney function over time. While iGFR declined overall, declines were attenuated among participants treated for HCV compared to participants who remained untreated.

Indexed as

Antiviral AgentsHepatitis C, ChronicRenal Insufficiency, ChronicAdultAlbuminuriaBiomarkersFemaleGlomerular Filtration RateHepacivirusHumansLongitudinal StudiesMaleMiddle AgedAntiviral AgentsBiomarkers

Identifiers

PMID40498739
PMCPMC12157062

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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.