Evidence map›Paper›PMID 25553110›Full record

Trial reportTheranostics2015

Quantitative hepatitis B core antibody level is a new predictor for treatment response in HBeAg-positive chronic hepatitis B patients receiving peginterferon.

Feng-Qin Hou, Liu-Wei Song, Quan Yuan, Lin-Lin Fang, Sheng-Xiang Ge, Jun Zhang, Ji-Fang Sheng, Dong-Ying Xie, Jia Shang, Shu-Huan Wu and 13 more

Abstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Theranostics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
–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

41 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. [Clinical significance and research progress of quantitative hepatitis B virus core antibody measurement].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2024
    Review
  7. [Research progress of biomarkers of hepatitis B virus and clinical significance].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2023
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Guidelines for Prevention and Treatment of Chronic Hepatitis B.Journal of clinical and translational hepatology · 2021
    Article
  17. [Correlation of qAnti-HBc with antiviral efficacy in children with chronic hepatitis B and exploration of its possible immune mechanism].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2021
    Article
  18. [Quantitative hepatitis B core antibody levels can be used as a predictive index of HBsAg clearance].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2021
    Article
  19. Article
  20. 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

23 authors.

Feng-Qin Hou1. Department of Infectious Diseases, Center for Liver Diseases, Peking University First Hospital, Beijing, China;
Liu-Wei Song2. State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Public Health, Xiamen University, Xiamen, China;
Quan Yuan2. State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Public Health, Xiamen University, Xiamen, China;
Lin-Lin Fang2. State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Public Health, Xiamen University, Xiamen, China;
Sheng-Xiang Ge2. State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Public Health, Xiamen University, Xiamen, China;
Jun Zhang2. State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Public Health, Xiamen University, Xiamen, China;
Ji-Fang Sheng3. Department of Infectious Diseases, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China;
Dong-Ying Xie4. Department of Infectious Diseases, the Third Affiliated Hospital of Sun Yet-Sen University, Guangzhou, China;
Jia Shang5. Department of Infectious Diseases, Henan Provincial People's Hospital, Zhengzhou, China;
Shu-Huan Wu6. Department of Infectious Diseases, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China;
Yong-Tao Sun7. Department of Infectious Diseases, Tang Du Hospital, the Fourth Military Medical University, Xi'an, China;
Shao-Feng Wei8. Department of Infectious Diseases, the First Affiliated Hospital of Anhui Medical University, Hefei, China;
Mao-Rong Wang9. Department of Infectious Diseases, PLA 81st Hospital, Nanjing, China;
Mo-Bin Wan10. Department of Infectious Diseases, the Second Military Medical University Changhai Hospital, Shanghai, China;
Ji-Dong Jia11. Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China;
Guang-Han Luo12. Department of Infectious Diseases, the First Affiliated Hospital of Guangxi Medical University, Nanning, China;
Hong Tang13. Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, China;
Shu-Chen Li14. Department of Infectious Diseases, the Second Affiliated Hospital of Harbin Medical University, Harbin, China;
Jun-Qi Niu15. Center for Liver Diseases, the First Affiliated Hospital of Changchun University, Changchun, China;
Wei-Dong Zhou16. Xiamen Amoytop Biotech Co. Ltd, Xiamen, China.
Li Sun16. Xiamen Amoytop Biotech Co. Ltd, Xiamen, China.
Ning-Shao Xia2. State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Public Health, Xiamen University, Xiamen, China;
Gui-Qiang Wang1. Department of Infectious Diseases, Center for Liver Diseases, Peking University First Hospital, Beijing, China;

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A recent study revealed that quantitative hepatitis B core antibody (qAnti-HBc) level could serve as a novel marker for predicting treatment response. In the present study, we further investigated the predictive value of qAnti-HBc level in HBeAg-positive patients undergoing PEG-IFN therapy. A total of 140 HBeAg-positive patients who underwent PEG-IFN therapy for 48 weeks and follow-up for 24 weeks were enrolled in this study. Serum samples were taken every 12 weeks post-treatment. The predictive value of the baseline qAnti-HBc level for treatment response was evaluated. Patients were further divided into 2 groups according to the baseline qAnti-HBc level, and the response rate was compared. Additionally, the kinetics of the virological and biochemical parameters were analyzed. Patients who achieved response had a significantly higher baseline qAnti-HBc level (serological response [SR], 4.52±0.36 vs. 4.19±0.58, p=0.001; virological response [VR], 4.53±0.35 vs. 4.22±0.57, p=0.005; combined response [CR], 4.50±0.36 vs. 4.22±0.58, p=0.009)). Baseline qAnti-HBc was the only parameter that was independently correlated with SR (p=0.008), VR (p=0.010) and CR(p=0.019). Patients with baseline qAnti-HBc levels ≥30,000 IU/mL had significantly higher response rates, more HBV DNA suppression, and better hepatitis control in PEG-IFN treatment. In conclusion, qAnti-HBc level may be a novel biomarker for predicting treatment response in HBeAg-positive patients receiving PEG-IFN therapy.

Indexed as

AdultBiomarkersDNA, ViralDrug MonitoringFemaleHepatitis B AntibodiesHepatitis B, ChronicHepatitis B Core AntigensHepatitis B e AntigensHumansInterferon-alphaMaleMiddle AgedPredictive Value of TestsPrognosisViral LoadBiomarkersDNA, ViralHepatitis B AntibodiesHepatitis B Core AntigensHepatitis B e AntigensInterferon-alphachronic hepatitis BPEG-IFN treatmentpretreatment biomarker.quantitative anti-HBctreatment response prediction

Identifiers

PMID25553110
PMCPMC4279186

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.