Evidence map›Paper›PMID 35709466›Full record

ArticlePloS one2022

Prognostic impact of steatosis in the clinical course of chronic HCV infection-Results from the German Hepatitis C-Registry.

Monika Rau, Peter Buggisch, Stefan Mauss, Klaus H W Boeker, Hartwig Klinker, Tobias Müller, Albrecht Stoehr, Jörn M Schattenberg, Andreas Geier

Open access · goldAbstract readMulticenter Study
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. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Steatotic liver disease and chronic viral hepatitis.Clinical and experimental hepatology · 2025
    Review
  5. Article
  6. Article
  7. Rising Lysophosphatidylcholine Levels Post-Hepatitis C Clearance.International journal of molecular sciences · 2024
    Article
  8. Review
  9. Article
  10. 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

9 authors at 5 institutions in 1 country.

Monika RauMedizinische Klinik II, Universitätsklinikum Würzburg, Würzburg, Germany.ORCID 0000-0003-1219-4044
Peter Buggischifi-Institute for Interdisciplinary Medicine, Hamburg, Germany.
Stefan MaussCenter for HIV and Hepatogastroenterology, Düsseldorf, Gernamny.
Klaus H W BoekerCenter of Hepatology, Hannover, Gernamny.
Hartwig KlinkerMedizinische Klinik II, Universitätsklinikum Würzburg, Würzburg, Germany.
Tobias MüllerCharité Campus Virchow-Klinikum (CVK), Berlin, Gernamny.
Albrecht Stoehrifi-Institute for Interdisciplinary Medicine, Hamburg, Germany.
Jörn M SchattenbergMetabolic Liver Research Program, University Medical Centre Mainz, Mainz, Germany.
Andreas GeierMedizinische Klinik II, Universitätsklinikum Würzburg, Würzburg, Germany.
Universitätsklinikum Würzburg · DEInstitute for Interdisciplinary Medicine · DECenter for HIV and Hepatogastroenterology · DECharité - Universitätsmedizin Berlin · DEJohannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLiver steatosis is often observed in chronic HCV infection and associated to genotype or comorbidities. NAFLD is an important risk factor for end-stage liver disease. We aimed to analyse the course of NAFLD as a concomitant disease in a cohort of HCV patients.

methodsThe German Hepatitis C-Registry is a national multicenter real-world cohort. In the current analysis, 8789 HCV patients were included and separated based on the presence of steatosis on ultrasound and/or histology. Fibrosis progression was assessed by transient elastography (TE), ultrasound or non-invasive surrogate scores.

resultsAt the time of study inclusion 12.3% (n = 962) of HCV patients presented with steatosis (+S) (higher rate in GT-3). Diabetes mellitus was more frequent in GT-1 patients. HCV patients without steatosis (-S) had a slightly higher rate of fibrosis progression (FP) over time (30.3%) in contrast to HCV patients +S (26%). This effect was mainly observed in GT-3 patients (34.4% vs. 20.6%). A larger decrease of ALT, AST and GGT from baseline to FU-1 (4-24 weeks after EOT) was found in HCV patients (without FP) +S compared to -S. HCV patients -S and with FP presented more often metabolic comorbidities with a significantly higher BMI (+0.58kg/m2) compared to patients -S without FP. This was particularly pronounced in patients with abnormal ALT.

conclusionClinically diagnosed steatosis in HCV patients does not seem to contribute to significant FP in this unique cohort. The low prevalence of steatosis could reflect a lower awareness of fatty liver in HCV patients, as patients -S and with FP presented more metabolic risk factors.

Indexed as

Hepatitis CHepatitis C, ChronicNon-alcoholic Fatty Liver DiseaseFibrosisHepacivirusHumansLiver CirrhosisPrognosisRegistries

Identifiers

PMID35709466
PMCPMC9203066
OpenAlexW4283034660

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.