Evidence map›Paper›PMID 36928343›Full record

Trial reportJournal of gastroenterology2023

High-risk population of progressive hepatic fibrosis in chronic hepatitis B patients on antiviral therapy.

Xiujuan Chang, Yinying Li, Chao Sun, Xiaodong Li, Wenjuan Du, Qinghua Shang, Laicheng Song, Qinghua Long, Qin Li, Huabao Liu and 9 more

Abstract readRandomized Controlled TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Journal of gastroenterology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Lower Serum HBV RNA Level is Associated with Liver Cirrhosis in Patients Treated with Nucleos(t)ide Analogs: A Population-Based Cross-Sectional Study.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
    Article
  3. Article
  4. 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

19 authors at 12 institutions in 1 country.

Xiujuan Chang *Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.ORCID http://orcid.org/0000-0002-4961-8560
Yinying Li *Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Chao Sun *Chinese PLA Medical School, Beijing, 100853, China.
Xiaodong Li *Department of Research for Clinical Medicine, the Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China.
Wenjuan DuDiscipline and Degree Division, the Graduate School of the PLA General Hospital, Beijing, 100853, China.
Qinghua ShangCenter of Therapeutic Liver Disease, the 88th Hospital of Chinese PLA, Taian, 271000, Shandong Province, China.
Laicheng SongTraditional Chinese Medicine Hospital of Taihe, Taihe, 400038, Anhui Province, China.
Qinghua LongDepartment of Infection and Liver Disease, Yichun People's Hospital, Yichun, Jiangxi Province, China.
Qin LiFuzhou Infectious Diseases Hospital, Fuzhou, 350025, Fujian Province, China.
Huabao LiuTraditional Chinese Medicine Hospital of Chongqing, Chongqing, 400038, China.
Jing WangAffiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, 610072, Sichuan Province, China.
Zujiang YuDepartment of Infectious Disease, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan Province, China.
Jiang LiDepartment of Infectious Diseases, Southwest Hospital, Army Military Medical University, Chongqing, 400038, China.
Guangming XiaoGuangzhou 8th People's Hospital, Guangzhou, 510060, Guangdong Province, China.
Li LiDepartment of Traditional Chinese Medicine, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Liang ChenDepartment of Hepatic Diseases, Shanghai Public Health Clinical Center, Shanghai, 201508, China.
Lin TanDepartment of Liver Disease, Fuyang 2nd People's Hospital, Fuyang, 236015, Anhui Province, China.
Yongping ChenDepartment of Infectious and Liver Diseases, Liver Research Center, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, Zhejiang Province, China. cyp@wmu.edu.cn.ORCID http://orcid.org/0000-0003-2806-4308
Yongping YangDepartment of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, 100039, China. yongpingyang@hotmail.com.ORCID http://orcid.org/0000-0002-8307-1095
Chinese PLA General Hospital · CNSouthwest Hospital · CN82th Hospital of Pla · CNFirst Affiliated Hospital of Zhengzhou University · CNFirst People's Hospital of Chongqing · CNFuyang Second People's Hospital · CNFuzhou Pulmonary Hospital of Fujian · CNGuangdong Provincial People's Hospital · CNShanghai Public Health Clinical Center · CNSouthwest Medical University · CNWenzhou Medical University · CNYichun University · CN

Funding

Major Science and Technology Special Project of China 2018ZX10725-506Natural Science Foundation of Beijing Municipality 7212101
6 · The paper itself

Abstract

backgroundProgressive hepatic fibrosis leads to hepatocellular carcinoma (HCC) and decompensated cirrhosis. The aim of this study was to identify the high-risk population for progressive hepatic fibrosis and the incidence of HCC and decompensated cirrhosis in chronic hepatitis B (CHB) patients with antiviral therapy.

methodsThe data came from a multicenter, center-randomized, double-blind clinical trial that analyzed only patients in the ETV-treated arm. There was 156 hepatitis B e antigen (HBeAg)-positive and 135 HBeAg-negative patients in 14 institutions. The primary endpoint was fibrosis reversal on 72-week Entecavir (ETV) treatment. The 7-year cumulative incidence of HCC and decompensated cirrhosis were analyzed. Multivariate logistic and LASSO regression analyses were used to screen variables associated with fibrosis reversal.

results86/156 (55%) HBeAg-positive and 58/135 (43%) HBeAg-negative patients achieved fibrosis reversal on 72-week ETV treatment. Average age was 43 years, 203 (69.8%) was male, and 144 (49.5%) patients had cirrhosis. Age ≥ 40 years (OR: 0.46, 95% CI 0.23-0.93) and HBcrAg ≥ 8.23 log U/ml (OR: 2.72, 95% CI 1.33-5.54) in HBeAg-positive patients and HBV genotype C (OR: 0.44, 95% CI 0.21-0.97) in HBeAg-negative patients were independent factors of fibrosis reversal. It was confirmed in patients with cirrhosis. After 7-year ETV treatment, seven (4.5%) HBeAg-positive patients occurred HCC or decompensated cirrhosis, including four patients with age ≥ 40 years and six with HBcrAg 8.23log U/ml, while twelve (8.9%) HBeAg-negative patients occurred, including eleven with HBV genotype C.

conclusionsHBeAg-positive patients with a low HBcrAg level or old age, and HBeAg-negative patients with HBV genotype C tended to develop progressive hepatic fibrosis and had a high incidence of HCC and decompensated cirrhosis, even on ETV treatment.

Indexed as

Carcinoma, HepatocellularHepatitis B, ChronicLiver NeoplasmsAdultAntiviral AgentsDNA, ViralHepatitis B e AntigensHepatitis B virusHumansLiver CirrhosisMaleAntiviral AgentsDNA, ViralHepatitis B e AntigensHBcrAgHBeAgHBsAgHepatic fibrosisHepatocellular carcinoma

Identifiers

PMID36928343
OpenAlexW4327675373

What OpenQuestion holds

Textmetadata
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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.