Evidence map›Paper›PMID 28208002›Full record

ArticleGut and liver2017

Expression of Hepatocyte Hepatitis B Core Antigen and Hepatitis B Surface Antigen as a Marker in the Management of Chronic Hepatitis B Patients.

Sun Young Yim, Tae Hyung Kim, Suh Sang Jun, Eun Sun Kim, Bora Keum, Yeon Seok Seo, Hyung Joon Yim, Yoon Tae Jeen, Hoon Jai Chun, Hong Sik Lee and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Gut and liver, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Observational
  6. Article
  7. 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

14 authors at 1 institution in 1 country.

Sun Young YimDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Tae Hyung KimDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Suh Sang JunDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Eun Sun KimDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Bora KeumDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Yeon Seok SeoDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Hyung Joon YimDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Yoon Tae JeenDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Hoon Jai ChunDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Hong Sik LeeDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Soon Ho UmDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Chang Duck KimDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Nam Hee WonDepartment of Pathology, Korea University College of Medicine, Seoul, Korea.
Ho Sang RyuDepartment of Internal Medicine, Korea University College of Medicine, Seoul, Korea.
Korea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsWe aimed to clarify the association of hepatitis B surface antigen (HBsAg)/hepatitis B core antigen (HBcAg) with the disease status and treatment response in patients with chronic hepatitis B (CHB).

methodsWe investigated 171 biopsy-proven entecavir-treated CHB patients (109 hepatitis B e antigen [HBeAg]-positive, 62 HBeAg-negative). HBcAg expression was positive when ≥10% of hepatocytes stained, and classified into nuclear, mixed, and cytoplasmic patterns. HBsAg expressions were intracytoplasmic (diffuse, globular, and submembranous) and membranous. The histologic activity index (HAI) and fibrosis stage followed Ishak system.

resultsIn HBeAg-positive patients, older age, increased HAI score, advanced fibrosis, and reduced viral load were observed when HBcAg expression shifted from nucleus to cytoplasm in HBcAg-positive patients, and HBsAg expression from non-submembranous to submembranous in HBcAg-negative patients (all, p<0.05). In HBeAg-negative patients, only intracytoplasmic HBsAg expression patterns had clinical relevance with decreased ALT levels and viremia. In HBeAg-positive patients without favorable predictors of virologic response, negative HBcAg and membranous HBsAg expression predicted greater virologic response (both, p<0.05). The probability of HBeAg seroclearance was higher in patients with increased HAI or lacking HBcAg expression (both, p<0.05). Higher serum HBsAg levels and hepatocyte HBcAg positivity were associated with reduced serum HBsAg during first and post-first year treatment, respectively (both, p<0.05).

conclusionsHepatocyte HBcAg/HBsAg expression is a good marker for disease status and predicting treatment response.

Indexed as

AdultAntiviral AgentsBiomarkersBiopsyFemaleGuanineHepatitis B, ChronicHepatitis B Core AntigensHepatitis B e AntigensHepatitis B Surface AntigensHepatitis B virusHepatocytesHumansLiverMaleMiddle AgedAntiviral AgentsBiomarkersentecavirGuanineHepatitis B Core AntigensHepatitis B e AntigensHepatitis B Surface AntigenschronicHepatitis BHepatitis B core antigensHepatitis B surface antigensHistologic activity index

Identifiers

PMID28208002
PMCPMC5417785
OpenAlexW2587898100

What OpenQuestion holds

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LicenceCC BY-NC
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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.