Evidence map›Paper›PMID 35482664›Full record

ArticlePloS one2022

Transient elastography score is elevated during rheumatoid factor-positive chronic hepatitis C virus infection and rheumatoid factor decline is highly variable over the course of direct-acting antiviral therapy.

Ann W N Auma, Corinne Kowal, Carey L Shive, Alyssa Lange, Sofi Damjanovska, Elizabeth Zebrowski, Elane Reyes, Leonard Calabrese, Lenche Kostadinova, Yngve Falck-Ytter and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. 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, top 95% of its field
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, 0 citations in OpenAlex.

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

12 authors at 4 institutions in 1 country.

Ann W N AumaDepartment of Pathology, Department of Medicine Case Western Reserve University, Cleveland, Ohio, United States of America.ORCID 0000-0002-0094-4007
Corinne KowalCleveland VA Medical Center and VA GRECC, Cleveland, Ohio, United States of America.
Carey L ShiveDepartment of Pathology, Department of Medicine Case Western Reserve University, Cleveland, Ohio, United States of America.
Alyssa LangeDepartment of Pathology, Department of Medicine Case Western Reserve University, Cleveland, Ohio, United States of America.
Sofi DamjanovskaCleveland VA Medical Center and VA GRECC, Cleveland, Ohio, United States of America.
Elizabeth ZebrowskiCleveland VA Medical Center and VA GRECC, Cleveland, Ohio, United States of America.
Elane ReyesCleveland VA Medical Center and VA GRECC, Cleveland, Ohio, United States of America.
Leonard CalabreseDepartment of Rheumatologic and Immunologic Disease, Cleveland Clinic Foundation, Cleveland, Ohio, United States of America.
Lenche KostadinovaCleveland VA Medical Center and VA GRECC, Cleveland, Ohio, United States of America.
Yngve Falck-YtterCleveland VA Medical Center and VA GRECC, Cleveland, Ohio, United States of America.
Maya MattarCleveland VA Medical Center and VA GRECC, Cleveland, Ohio, United States of America.
Donald D AnthonyDepartment of Pathology, Department of Medicine Case Western Reserve University, Cleveland, Ohio, United States of America.ORCID 0000-0002-1226-5976
Geriatric Research Education and Clinical Center · USCase Western Reserve University · USCleveland Clinic · USMetroHealth · US

Funding

Microbiology and Immunology Training for HIV and HIV-Related Research in Uganda (MITHU)D43TW010319 · FIC · CASE WESTERN RESERVE UNIVERSITY · PI BOOM, W. HENRY, JOLOBA, MOSES LUTAAKOME · 2016 to 2025
$3.1M
Role of NK cells in control of HCV infection associated hepatocellular carcinomaI01BX001894 · VA · LOUIS STOKES CLEVELAND VA MEDICAL CENTER · PI Donald D Anthony · 2013 to 2026
–
Role of ENPP2, immune activation and age on neoantigen response during HCVI01CX001104 · VA · LOUIS STOKES CLEVELAND VA MEDICAL CENTER · PI ANTHONY, DONALD D · 2015 to 2018
–
Impact of Immune Activation on Cardiovascular and Immune Health in RAI01CX001791 · VA · LOUIS STOKES CLEVELAND VA MEDICAL CENTER · PI ANTHONY, DONALD D · 2020 to 2024
–
BLRD VA I01 BX001894CSRD VA I01 CX001104CSRD VA I01 CX001791CSRD VA IK2 CX001471FIC NIH HHS D43 TW010319
6 · The paper itself

Abstract

backgroundElevated rheumatoid factor (RF) levels and systemic immune activation are highly prevalent during chronic hepatitis C virus (HCV) infection. Direct-acting antiviral (DAA) therapy has been associated with normalization of various soluble immune activation parameters. Whether the RF levels relate to soluble immune activation markers during chronic HCV infection, and over what time frame RF levels normalize during and after DAA treatment is unknown and was investigated here.

methodsIn a longitudinal study, plasma and serum was obtained from HCV infected RF positive (RF+) and RF negative (RF-) participants. The levels of RF, HCV RNA and soluble markers of inflammation were determined before (week 0), during (weeks 4, 8 and 12) and after (week 24) treatment with HCV DAA therapy. In a subset of RF+ participants, the analysis was extended to over 70 weeks after therapy initiation. Hepatic and other clinical parameters were determined at baseline (week 0) in all participants.

resultsBefore therapy, transient elastography (TE) score was greater in RF+ compared to RF- HCV infected participants, while the systemic levels of soluble inflammatory markers were comparable. Following DAA therapy initiation, HCV RNA levels became undetectable within 4 weeks in both the RF+ and RF- groups. RF levels declined in the first 6 months in most RF+ persons but most commonly remained positive. The levels of some soluble inflammatory markers declined, mainly within 4 weeks of DAA therapy start, in both the RF+ and RF- groups. The baseline (week 0) TE score correlated with RF levels before, during and after DAA therapy, while plasma IL-18 levels correlated with RF level after DAA therapy.

conclusionDuring chronic HCV infection, TE score is elevated in RF+ HCV infected individuals and factors other than HCV viremia (including liver stiffness or fibrosis and select markers of inflammation) likely contribute to persistence of RF after treatment of HCV with DAA.

Indexed as

Elasticity Imaging TechniquesHepatitis C, ChronicAntiviral AgentsBiomarkersHumansInflammationLongitudinal StudiesRheumatoid FactorRNAAntiviral AgentsBiomarkersRheumatoid FactorRNA

Identifiers

PMID35482664
PMCPMC9049346
OpenAlexW4224989602

What OpenQuestion holds

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LicenceCC0
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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.