Evidence map›Paper›PMID 26527281›Full record

ArticleVirology journal2015

A model with combined viral and metabolic factors effectively predicts HBeAg status under long term entecavir therapy: a prospective cohort study.

Fen Liu, Feng Zou, Xiwei Wang, Huaidong Hu, Peng Hu, Hong Ren

Abstract read
In one paragraph

Article in Virology journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Fen LiuDepartment of Infectious Diseases, Second Affiliated Hospital of Chongqing Medical University, Linjiang Road, Yuzhong District, Chongqing, China. liu2011fen@163.com.
Feng ZouDepartment of Infectious Diseases, Second Affiliated Hospital of Chongqing Medical University, Linjiang Road, Yuzhong District, Chongqing, China. 15123324016@163.com.
Xiwei WangDepartment of Infectious Diseases, Second Affiliated Hospital of Chongqing Medical University, Linjiang Road, Yuzhong District, Chongqing, China. yidaxiwei@126.com.
Huaidong HuDepartment of Infectious Diseases, Second Affiliated Hospital of Chongqing Medical University, Linjiang Road, Yuzhong District, Chongqing, China. huaidong.hu@gmail.com.
Peng HuDepartment of Infectious Diseases, Second Affiliated Hospital of Chongqing Medical University, Linjiang Road, Yuzhong District, Chongqing, China. hp_cq@163.com.
Hong RenDepartment of Infectious Diseases, Second Affiliated Hospital of Chongqing Medical University, Linjiang Road, Yuzhong District, Chongqing, China. renhong0531@vip.sina.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimThe aim was to extract factors from virologic and biochemical profiles at baseline and 24 weeks of treatment to predict HBeAg seroconversion in patients treated with ETV.

methodsHBeAg positive chronic hepatitis B patients receiving ETV naïve-treatment were enrolled. HBV DNA, ALT, and serological markers were prospectively monitored every 6 months for 240 weeks. The cumulative rates of virologic response (VR), biochemical response (BR), and HBeAg seroconversion were determined, and potential predictors for HBeAg seroconversion were identified through uni/multivariate analysis.

resultTwo hundred twenty nine patients were eligible for this study. The cumulative rates of VR, BR, and HBeAg seroconversion at 240 weeks were 88.4 %, 100 %, and 36.7 %, respectively. Multivariate analysis showed that HBV DNA (OR, 2.8, p = 0.003), ALT (OR, 2.6, p = 0.005) at baseline, undetectable HBV DNA within 24 weeks (OR = 3.2, p < 0.001), and body mass index (BMI) ≥24kg/m(2) (OR = 0.038, p = 0.013) were associated with HBeAg seroconversion. A prediction model for probability of HBeAg seroconversion was constructed. Patients can be classified into high (>40 %), intermediate (20-40 %), or low (≤20 %) groups based on the calculated probability of HBeAg seroconversion. The cumulative rates of HBeAg seroconversion were different among the three groups (p < 0.001). About 58 % patients in the high probability group achieved HBeAg seroconversion while almost 90 % patients within the low group remained HBeAg positive.

conclusionA combination of HBV DNA, ALT and BMI values at baseline, and undetectable HBV DNA level within 24 weeks can predict HBeAg seroconversion. Both viral and metabolic factors likely determine HBeAg status with ETV treatment.

trial registrationCTR20132358.

Indexed as

Body Mass IndexAdultAlanine TransaminaseAntiviral AgentsDNA, ViralFemaleGuanineHepatitis B, ChronicHepatitis B e AntigensHumansLongitudinal StudiesMaleModels, StatisticalPrognosisProspective StudiesTreatment OutcomeAlanine TransaminaseAntiviral AgentsDNA, ViralentecavirGuanineHepatitis B e Antigens

Identifiers

PMID26527281
PMCPMC4630878

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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.