Evidence map›Paper›PMID 41221672›Full record

ArticleEmerging microbes & infections2025

Antiviral treatment response to nucleos(t)ide analogues in chronic hepatitis B patients with normal alanine aminotransferase levels: a retrospective multi-center study.

Fei Cao, Jian Wang, Ye Xiong, Ying Zhang, Xinrong Zhang, Tao Fan, Li Zhu, Shaoqiu Zhang, Zhiyi Zhang, Yifan Pan and 10 more

Abstract readMulticenter Study
In one paragraph

Article in Emerging microbes & infections, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Fei CaoDepartment of Infectious Diseases, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, People's Republic of China.
Jian WangDepartment of Infectious Diseases, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic of China.
Ye XiongDepartment of Infectious Diseases, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, People's Republic of China.
Ying ZhangPrenatal diagnosis center, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, People's Republic of China.
Xinrong ZhangDivision of Gastroenterology and Hepatology, School of Medicine, Stanford University, Palo Alto, CA, USA.
Tao FanDepartment of Infectious Diseases, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, People's Republic of China.
Li ZhuDepartment of Infectious Diseases, The Affiliated Infectious Diseases Hospital of Soochow University, Suzhou, People's Republic of China.
Shaoqiu ZhangDepartment of Infectious Diseases, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic of China.
Zhiyi ZhangDepartment of Infectious Diseases, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, People's Republic of China.
Yifan PanDepartment of Infectious Diseases, Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University, Nanjing, People's Republic of China.
Yuanyuan LiDepartment of Infectious Diseases, Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University, Nanjing, People's Republic of China.
Chao JiangDepartment of Infectious Diseases, Nanjing Drum Tower Hospital Clinical College of Jiangsu University, Nanjing, People's Republic of China.
Juan XiaDepartment of Infectious Diseases, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic of China.
Yu ShiState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, People's Republic of China.
Xiaomin YanDepartment of Infectious Diseases, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic of China.
Yuxin ChenDepartment of Laboratory Medicine, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, People's Republic of China.
Xingxiang LiuDepartment of Clinical Laboratory, Huai'an No. 4 People's Hospital, Huai'an, People's Republic of China.
Chuanwu ZhuDepartment of Infectious Diseases, The Affiliated Infectious Diseases Hospital of Soochow University, Suzhou, People's Republic of China.
Chao WuDepartment of Infectious Diseases, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, People's Republic of China.
Rui HuangDepartment of Infectious Diseases, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhether patients with chronic hepatitis B (CHB) with normal alanine aminotransferase (ALT) levels should receive antiviral therapy remains controversial. We compared the efficacy of nucleos(t)ide analogs (NAs) among CHB patients with different baseline ALT levels.

methodsA total of 1,204 treatment-naïve CHB patients with detectable hepatitis B virus (HBV) DNA levels who initiated first-line NAs treatment were retrospectively included from three hospitals and followed up for 96 weeks. Virological response (VR) and HBeAg serological responses were compared among patients with different baseline ALT levels.

resultsOf the total patients, 682 (56.6%) were HBeAg-positive at baseline. In patients with normal ALT levels, 44.9% and 69.4% of HBeAg-positive patients achieved VR at weeks 48 and 96, respectively, whereas VR rates were 91.2% and 91.9% in HBeAg-negative patients, respectively. In the multivariate Cox regression analysis, baseline ALT ≤ 1×upper limit of normal (ULN) and ALT 1-2×ULN were not associated with VR compared to ALT > 2×ULN. However, the cumulative incidence of HBeAg clearance and seroconversion was significantly lower in patients with ALT ≤ 1×ULN than in those with ALT > 2×ULN (both P < 0.001). Baseline ALT ≤ 1×ULN was associated with a significantly lower chance of achieving HBeAg clearance (HR = 0.314, 95% CI: 0.163-0.607, P = 0.001) and HBeAg seroconversion (HR = 0.280, 95% CI: 0.127-0.615, P = 0.002).

conclusionsCHB patients with normal ALT levels had comparable VR rates but significantly lower rates of HBeAg clearance and seroconversion during first-line NA therapy than patients with elevated ALT levels.

Indexed as

Alanine TransaminaseAntiviral AgentsHepatitis B, ChronicNucleosidesNucleotidesAdultDNA, ViralFemaleHepatitis B e AntigensHepatitis B virusHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeYoung AdultAlanine TransaminaseAntiviral AgentsDNA, ViralHepatitis B e AntigensNucleosidesNucleotidesalanine aminotransferaseChronic hepatitis Bnucleoside/nucleotide analoguestreatment response

Identifiers

PMID41221672
PMCPMC12667291

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.