Evidence map›Paper›PMID 27510387›Full record

ArticleJournal of Korean medical science2016

Clinical Utility of a New Automated Hepatitis C Virus Core Antigen Assay for Prediction of Treatment Response in Patients with Chronic Hepatitis C.

Mi Na Kim, Hyon Suk Kim, Ja Kyung Kim, Beom Kyung Kim, Seung Up Kim, Jun Yong Park, Do Young Kim, Sang Hoon Ahn, Kwang Hyub Han

Open access · goldAbstract read
In one paragraph

Article in Journal of Korean medical science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Review
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

9 authors at 1 institution in 1 country.

Mi Na KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0001-5381-230X
Hyon Suk KimDepartment of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0001-5662-7740
Ja Kyung KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0001-5025-6846
Beom Kyung KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0002-5363-2496
Seung Up KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0002-9658-8050
Jun Yong ParkDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0001-6324-2224
Do Young KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0002-8327-3439
Sang Hoon AhnDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0002-3629-4624
Kwang Hyub HanDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea. gihankhys@yuhs.ac.ORCID http://orcid.org/0000-0003-3960-6539
Yonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis C virus core antigen (HCV Ag) is a recently developed marker of hepatitis C virus (HCV) infection. We investigated the clinical utility of the new HCV Ag assay for prediction of treatment response in HCV infection. We analyzed serum from 92 patients with HCV infection who had been treated with pegylated interferon and ribavirin. HCV Ag levels were determined at baseline in all enrolled patients and at week 4 in 15 patients. Baseline HCV Ag levels showed good correlations with HCV RNA (r = 0.79, P < 0.001). Mean HCV Ag levels at baseline were significantly lower in patients with a sustained virologic response (SVR) than in those with a non SVR (relapse plus non responder) based on HCV RNA analysis (2.8 log₁₀fmol/L vs. 3.27 log₁₀fmol/L, P = 0.023). Monitoring of the viral kinetics by determination of HCV RNA and HCV Ag levels resulted in similarly shaped curves. Patients with undetectable HCV Ag levels at week 4 had a 92.3% probability of achieving SVR based on HCV RNA assay results. The HCV Ag assay may be used as a supplement for predicting treatment response in HCV infection, but not as an alternative to the HCV RNA assay.

Indexed as

Antigens, ViralAntiviral AgentsAutomationDrug Therapy, CombinationFemaleGenotypeHepacivirusHepatitis C, ChronicHumansImmunoassayInterferon-alphaMaleMiddle AgedPolyethylene GlycolsPolymerase Chain ReactionReagent Kits, DiagnosticAntigens, ViralAntiviral AgentsInterferon-alphapeginterferon alfa-2aPolyethylene GlycolsReagent Kits, DiagnosticRecombinant ProteinsRibavirinRNA, ViralChronic Hepatitis CHCV Core AntigenHCV RNATreatment Response

Identifiers

PMID27510387
PMCPMC4974185
OpenAlexW2469957755

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.