Evidence map›Paper›PMID 33889834›Full record

ArticleMetabolism open2021

Non-alcoholic fatty liver disease is a risk factor for occurrence of hepatocellular carcinoma after sustained virologic response in chronic hepatitis C patients: A prospective four-years follow-up study.

Dong Ji, Guo-Feng Chen, Xiao-Xia Niu, Mingjie Zhang, Cheng Wang, Qing Shao, Vanessa Wu, Yudong Wang, Gregory Cheng, Selwyn J Hurwitz and 2 more

Open access · goldAbstract read
In one paragraph

Article in Metabolism open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the 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
3.2field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Steatotic liver disease and chronic viral hepatitis.Clinical and experimental hepatology · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Noninvasive Fibrosis Assessment in Chronic Hepatitis C Infection: An Update.Journal of clinical and translational hepatology · 2023
    Review
  11. Review
  12. Observational
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. 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

12 authors at 3 institutions in 3 countries.

Dong JiDepartment of Liver Diseases, Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Guo-Feng ChenDepartment of Liver Diseases, Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Xiao-Xia NiuDepartment of Liver Diseases, Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Mingjie ZhangFaculty of Health Science, Macau University, Taipa, Macau.
Cheng WangFifth Medical Center of Chinese PLA General Hospital-Hong Kong Humanity and Health Hepatitis C Diagnosis and Treatment Centre, Beijing, 100039, China.
Qing ShaoDepartment of Liver Diseases, Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Vanessa WuFifth Medical Center of Chinese PLA General Hospital-Hong Kong Humanity and Health Hepatitis C Diagnosis and Treatment Centre, Beijing, 100039, China.
Yudong WangFifth Medical Center of Chinese PLA General Hospital-Hong Kong Humanity and Health Hepatitis C Diagnosis and Treatment Centre, Beijing, 100039, China.
Gregory ChengFaculty of Health Science, Macau University, Taipa, Macau.
Selwyn J HurwitzCenter for AIDS Research, Laboratory of Biochemical Pharmacology, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, 30322, USA.
Raymond F SchinaziCenter for AIDS Research, Laboratory of Biochemical Pharmacology, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, 30322, USA.
George LauDepartment of Liver Diseases, Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Chinese PLA General Hospital · CNEmory University · USUniversity of Macau · MO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimThe incidence of hepatocellular carcinoma (HCC) decreases significantly in chronic hepatitis C (CHC) patients with sustained virologic response (SVR) after pegylated-interferon plus ribavirin (PR) or direct-acting antiviral (DAAs) therapy. We follow-up a single cohort of CHC patients to identify risk factors associated with HCC development post-SVR.

methodCHC patients with SVR in Beijing/Hong Kong were followed up at 12-24 weekly intervals with surveillance for HCC by ultrasonography and alpha-fetoprotein (AFP). Multivariate Cox proportional hazards regression analysis was used to explore factors associated with HCC occurrence.

resultsBetween October 2015 and May 2017, SVR was observed in 519 and 817 CHC patients after DAAs and PR therapy respectively. After a median post -SVR follow-up of 48 months, HCC developed in 54 (4.4%) SVR subjects. By adjusted Cox analysis, older age (≥55 years) [HR 2.4, 95% CI (1.3-4.3)], non-alcoholic fatty liver diseases [HR 2.4, 95%CI (1.3-4.2), higher AFP level (≥20 ng/ml) [HR 3.4, 95%CI (2.0-5.8)], higher liver stiffness measurement (≥14.6 kPa) [HR 4.2, 95%CI (2.3-7.6)], diabetes mellitus [HR 4.2, 95%CI (2.4-7.4)] at pre-treatment were associated with HCC occurrence. HCC patients in the DAAs induced SVR group had a higher prevalence of NAFLD as compared with those in the PR induced SVR group, 62% (18/29) vs 28% (7/25), p = 0.026. A nomogram formulated with the above six independent variables had a Concordance-Index of 0.835 (95% CI 0.783-0.866).

conclusionUnderlying NAFLD is associated with increased incidence of HCC in chronic HCV patients post-SVR, particularly in those treated with DAA.

Indexed as

AFP, alpha-fetoproteinALT, alanine aminotransferaseANGPTL, angiopoietin-like proteinsAST, aspartate aminotransferaseASV, asunaprevirBCLC, Barcelona-Clinic Liver Cancer GroupBMI, body mass indexCHC, chronic hepatitis CChronic hepatitis CCI, confidence intervals (CI)DAAs, direct-acting antiviral agentsDCV, daclatasvirFGF, fibroblast growth factorHCCHCC, hepatocellular carcinomaHCV, hepatitis C virusHR, Hazard RatioIFN, interferonLDV, ledipasvirLSM, liver stiffness measurementNAFLDPeg-IFN, Pegylated interferonPLT, platelet countPR, Peg-IFN-α with RBVRBV, ribavirinSMV, simeprevirSOF, sofosbuvirSustained virologic responseSVR, sustained virologic responseTBIL, total bilirubinTNF, tumor necrosis factorULN, upper limit of normal

Identifiers

PMID33889834
PMCPMC8050772
OpenAlexW3147504909

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.