Evidence map›Paper›PMID 38487738›Full record

ArticleHepatology forum2024

HBV viral load and tumor and non-tumor factors in patients with HBV-associated HCC.

Engin Ataman, Murat Harputluoglu, Brian Irving Carr, Harika Gozukara, Volkan Ince, Sezai Yilmaz

Abstract read
In one paragraph

Article in Hepatology forum, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

6 authors.

Engin AtamanDepartment of Gastroenterology and Hepatology, Inonu University Medical Faculty Liver Transplant Institute, Malatya, Turkiye.
Murat HarputluogluDepartment of Gastroenterology and Hepatology, Inonu University Medical Faculty Liver Transplant Institute, Malatya, Turkiye.
Brian Irving CarrInonu University Medical Faculty Liver Transplant Institute, HCC Translational Research Unit, Malatya, Turkiye.
Harika GozukaraDepartment of Biostatistic, Inonu University School of Medicine, Malatya, Turkiye.
Volkan InceDepartment of General Surgery, Inonu University School of Medicine, Liver Transplant Institute, Malatya, Turkiye.
Sezai YilmazDepartment of General Surgery, Inonu University School of Medicine, Liver Transplant Institute, Malatya, Turkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: Several tumor and non-tumor factors affect the prognosis of hepatocellular carcinoma (HCC) patients. This study aimed to investigate the effects of hepatitis B virus (HBV) viral load on tumor and non-tumor factors in patients with HBV-associated HCC. Materials and Methods: Patients with hepatitis B and HCC who presented to the HCC council at the Faculty of Medicine, Marmara University Liver Transplantation Institute, were included in our study. Patients were divided into two groups according to the presence or absence of HBV-DNA, and it was determined whether there were differences between these two groups with respect to tumor and non-tumor parameters. Results: Comparison of serum alanine aminotransferase (ALT), gamma-glutamyl transferase (GGT), hepatitis B surface antigen (HBsAg), and C-reactive protein (CRP) levels between HBV-DNA negative and positive patients showed significant differences (respectively p<0.01, p<0.01, p<0.05, and p<0.05). A major finding was a very significant difference between the two patient groups in terms of portal vein invasion (PVI) and venous invasion (p<0.001 and p<0.01, respectively). However, there was no significant difference in metastasis or lymph node involvement between HBV-DNA negative and positive patients. Conclusion: Our findings suggest that HBV viral load plays an important role in PVI in HCC patients, and there is a significant relationship between HBV viral load and inflammation.

Indexed as

HBV-DNAHepatitis Bhepatocellular carcinoma

Identifiers

PMID38487738
PMCPMC10936120

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