Evidence map›Paper›PMID 38633437›Full record

ArticleInfectious diseases & clinical microbiology2024

Predictors of Significant Histological Hepatic Abnormality in Treatment-Naive Patients Infected with HBeAg-Negative Chronic Hepatitis B.

Gülşah Tunçer, Ceyda Geyiktepe-Güçlü, Osman Faruk Bayramlar, Burcu Atasoy-Bozan, Çiğdem Yücel, Serkan Sürme, Betül Çopur, Kadir Görkem Güçlü, Khalis Mustafayev, Türkan İkizceli and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Infectious diseases & clinical microbiology, 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, 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

2 citing papers in PubMed, 0 citations in OpenAlex.

  1. Article
  2. 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

14 authors at 3 institutions in 2 countries.

Gülşah TunçerDepartment of Infectious Diseases and Clinical Microbiology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0000-0002-9841-9146
Ceyda Geyiktepe-GüçlüDepartment of Infectious Diseases and Clinical Microbiology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0009-0008-7561-6842
Osman Faruk BayramlarBakırköy District Health Directorate, İstanbul, Türkiye.ORCID https://orcid.org/0000-0001-7311-3258
Burcu Atasoy-BozanDepartment of Infectious Diseases and Clinical Microbiology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0009-0006-5284-7598
Çiğdem YücelDepartment of Infectious Diseases and Clinical Microbiology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0009-0000-0923-4987
Serkan SürmeDepartment of Medical Microbiology, İstanbul University-Cerrahpaşa, İstanbul, Türkiye.ORCID https://orcid.org/0000-0001-7239-1133
Betül ÇopurDepartment of Infectious Diseases and Clinical Microbiology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0000-0001-5534-1388
Kadir Görkem GüçlüDepartment of Infectious Diseases and Clinical Microbiology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0000-0002-2682-7570
Khalis MustafayevDepartment of Infectious Diseases, Infection Control and Employee Health, University of Texas, MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-4616-2430
Türkan İkizceliDepartment of Radiology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0000-0002-5683-0391
Esen Gül UzunerDepartment of Medical Pathology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0000-0002-2732-1651
Mustafa YıldırımDepartment of Infectious Diseases and Clinical Microbiology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0000-0001-8165-1814
Gönül ŞengözDepartment of Infectious Diseases and Clinical Microbiology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0000-0002-1950-7288
Filiz PehlivanogluDepartment of Infectious Diseases and Clinical Microbiology, Haseki Training Research Hospital, İstanbul, Türkiye.ORCID https://orcid.org/0000-0001-9943-6004
Haseki Eğitim ve Araştırma Hastanesi · TRIstanbul University-Cerrahpaşa · TRThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study aimed to determine the predictors for significant hepatic abnormality (SHA), a treatment indication, by assessing demographic, laboratory, and radiological results of chronic hepatitis B (CHB) patients who underwent liver biopsy. Materials and Methods: In this retrospective study, individuals with untreated hepatitis B e-antigen (HBeAg)-negative CHB infection were enrolled. Multivariate analysis modeling was conducted with parameters identified as predictors for SHA in univariate analysis. Optimal threshold levels for variables to predict SHA in patients with chronic hepatitis B were determined based on receiver operating characteristic (ROC) curve analysis. Results: A total of 566 patients with untreated chronic hepatitis B were included in the cohort; 61% (345/566) were male, and the median age was 41 years (interquartile range [IQR]=34-50). Notably, 36.9% (209/566) had SHA. In the multivariate analysis, utilizing different models, age, gender, HBV-DNA, LDL, ALT, and platelet count were identified as the most reliable predictors for SHA in CHB patients. For predicting SHA, the area under the ROC curve values of HBV-DNA, AST, and ALT were 0.704 (sensitivity=62.8%, specificity=76.2%; Conclusion: In our study, age, male gender, ALT, AST, HBV-DNA, LDL cholesterol, platelet count, and FIB-4 score were independent predictors of SHA in HBeAg-negative chronic hepatitis B. The most sensitive parameters for SHA were LDL and ALT. The most specific parameters were age, AST, and APRI score. SHA may occur in patients with high HBV-DNA levels, even if ALT values are normal in HBeAg-negative patients.

Indexed as

ALTchronic hepatitis Bfibrosis scoreHAI scoreHBV- DNA

Identifiers

PMID38633437
PMCPMC11019720
OpenAlexW4392697765

What OpenQuestion holds

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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.