Evidence map›Paper›PMID 28229987›Full record

ArticleChinese medical journal2017

Kinetics of Hepatitis B Surface Antigen Level in Chronic Hepatitis B Patients who Achieved Hepatitis B Surface Antigen Loss during Pegylated Interferon Alpha-2a Treatment.

Ming-Hui Li, Lu Zhang, Xiao-Jing Qu, Yao Lu, Ge Shen, Shu-Ling Wu, Min Chang, Ru-Yu Liu, Lei-Ping Hu, Zhen-Zhen Li and 3 more

Abstract read
In one paragraph

Article in Chinese medical journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

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

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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

13 authors.

Ming-Hui LiLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Lu ZhangLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Xiao-Jing QuLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Yao LuLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Ge ShenLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Shu-Ling WuLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Min ChangLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Ru-Yu LiuLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Lei-Ping HuLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Zhen-Zhen LiLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Wen-Hao HuaClinical Test Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Shu-Jing SongClinical Test Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Yao XieLiver Diseases Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatitis B surface antigen (HBsAg) loss/seroconversion is considered to be the ideal endpoint of antiviral therapy and the ultimate treatment goal in chronic hepatitis B (CHB). This study aimed to assess the patterns of HBsAg kinetics in CHB patients who achieved HBsAg loss during the treatment of pegylated interferon (PEG-IFN) α-2a.

methodsA total of 150 patients were enrolled, composing of 83 hepatitis B envelope antigen (HBeAg)-positive and 67 HBeAg-negative patients. Patients were treated with PEG-IFN α-2a180 μg/week until HBsAg loss/seroconversion was achieved, which occurred within 96 weeks. Serum hepatitis B virus deoxyribonucleic acid and serological indicators (HBsAg, anti-HBs, HBeAg, and anti-HBe) were determined before and every 3 months during PEG-IFN α-2a treatment. Biochemical markers and peripheral blood neutrophil and platelet counts were tested every 1-3 months.

resultsBaseline HBsAg levels were 2.5 ± 1.3 log IU/ml, and decreased rapidly at 12 and 24 weeks by 48.3% and 88.3%, respectively. The mean time to HBsAg loss was 54.2 ± 30.4 weeks, though most patients needed extended treatment and 30.0% of HBsAg loss occurred during 72-96 weeks. Baseline HBsAg levels were significantly higher in HBeAg-positive patients (2.9 ± 1.1 log IU/ml) compared with HBeAg-negative patients (2.0 ± 1.3 log IU/ml; t = 4.733, P < 0.001), but the HBsAg kinetics were similar. Patients who achieved HBsAg loss within 48 weeks had significantly lower baseline HBsAg levels and had more rapid decline of HBsAg at 12 weeks compared to patients who needed extended treatment to achieve HBsAg loss.

conclusionsPatients with lower baseline HBsAg levels and more rapid decline during early treatment with PEG-IFN are more likely to achieve HBsAg loss during 96 weeks of treatment, and extended therapy longer than 48 weeks may be required to achieve HBsAg loss.

Indexed as

Antiviral AgentsDrug Administration ScheduleHepatitis B, ChronicHepatitis B Surface AntigensHumansInterferon-alphaKineticsPolyethylene GlycolsRecombinant ProteinsRetrospective StudiesTreatment OutcomeAntiviral AgentsHepatitis B Surface AntigensInterferon-alphapeginterferon alfa-2aPolyethylene GlycolsRecombinant Proteins

Identifiers

PMID28229987
PMCPMC5339929

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.