Evidence map›Paper›PMID 27485356›Full record

ArticleThe Journal of infectious diseases2016

Fibrosis Progression in Patients With Chronic Hepatitis C Virus Infection.

Marija Zeremski, Rositsa B Dimova, Jaroslaw Pillardy, Ype P de Jong, Ira M Jacobson, Andrew H Talal

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03025074 (Virology, Immunology and Mechanisms of Liver Disease in Patients With Hepatitis C and Other Liver Diseases), which is not on this map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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.

NCT03025074 recruitingnot on this map

Virology, Immunology and Mechanisms of Liver Disease in Patients With Hepatitis C and Other Liver Diseases

Typeobservational_patient_registrySponsorState University of New York at BuffaloRan2013 to 2099Enrolled1,000ConditionsNon-Alcoholic Steatohepatitis(NASH), Hepatitis C, Hepatitis B, Fibrosis
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Distribution and inflammatory potential of hepatitis C virus genotypes in the United States, 2011-2020.JGH open : an open access journal of gastroenterology and hepatology · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Epidemiology of Hepatitis C.Clinical liver disease · 2018
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Marija ZeremskiDivision of Gastroenterology and Hepatology, Weill Cornell Medical College.
Rositsa B DimovaDivision of Gastroenterology, Hepatology, and Nutrition, Department of Medicine Department of Biostatistics, State University of New York, Buffalo.
Jaroslaw PillardyInstitute for Biotechnology, Cornell University, Ithaca, New York.
Ype P de JongDivision of Gastroenterology and Hepatology, Weill Cornell Medical College.
Ira M JacobsonIcahn School of Medicine at Mount Sinai, New York.
Andrew H TalalDivision of Gastroenterology and Hepatology, Weill Cornell Medical College Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine.
Cornell University · USIcahn School of Medicine at Mount Sinai · USUniversity at Buffalo, State University of New York · US

Funding

The role of innate immune evasion in hepatitis C virus infectionK08DK090576 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI DE JONG, YPE PETER · 2011 to 2015
$760k
NIDDK NIH HHS K08 DK090576
6 · The paper itself

Abstract

backgroundFibrosis progression varies markedly in hepatitis C virus (HCV)-infected individuals. We investigated factors that influence fibrosis progression in chronic HCV infection.

methodsHCV-infected patients who underwent at least 2 liver biopsies were included in this study. Associations between fibrosis progression and epidemiologic, virologic, and disease-associated factors were analyzed using logistic regression and multistate Markov modeling.

resultsWe analyzed 936 biopsy specimens obtained from 378 individuals. Mean age (±SD) at first biopsy was 48.3 ± 9.3 years, 59.3% of patients were male, 59.9% were white, and 86.7% were infected with HCV genotype 1. Fibrosis progression and cirrhosis occurred in 57.4% and 5.8%, respectively. Fibrosis progression between the first and last biopsies was associated with lower fibrosis in the first biopsy specimen (P < .001) and with the occurrence of at least 1 flare in the alanine aminotransferase (ALT) level (>200 U/L; P = .007). We found the highest fibrosis progression rate between stages 0 and 1 and the lowest between stages 2 and 3. Increased necroinflammation and higher ALT level were associated with faster progression. HCV genotype 3-infected patients were more likely to progress to cirrhosis (P < .001).

conclusionsFibrosis progression in HCV is not linear but varies according to stage, with the highest progression in patients with the lowest fibrosis severity. Patients who experience flares in the ALT level are also more likely to progress.

Indexed as

Alanine TransaminaseBiopsyDisease ProgressionFemaleHepacivirusHepatitis C, ChronicHumansLiver CirrhosisMaleMiddle AgedRNA, ViralAlanine TransaminaseRNA, Viralalanine aminotransferasecirrhosisliver biopsyliver disease progressionviral hepatitis

Identifiers

PMID27485356
PMCPMC6281340
OpenAlexW2483257947

What OpenQuestion holds

Textmetadata
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Registered trials

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.