Evidence map›Paper›PMID 24348634›Full record

ArticleHepatitis monthly2013

Evaluation of PCR-RFLP in the Pre-S Region as Molecular Method for Hepatitis B Virus Genotyping.

Rim Ouneissa, Olfa Bahri, Ahlem Ben Yahia, Henda Touzi, Mohamed Msaddak Azouz, Nabyl Ben Mami, Henda Triki

Open access · hybridAbstract read
In one paragraph

Article in Hepatitis monthly, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 32% 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, 7 citations in OpenAlex.

  1. Article
  2. Untypable genotype restriction patterns and surface gene variants of hepatitis B virus isolates.International journal of molecular epidemiology and genetics · 2017
    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

7 authors at 3 institutions in 1 country.

Rim OuneissaLaboratory of Clinical Virology, Institute Pasteur de Tunis, Tunis, Tunisia.
Olfa BahriLaboratory of Clinical Virology, Institute Pasteur de Tunis, Tunis, Tunisia.
Ahlem Ben YahiaLaboratory of Clinical Virology, Institute Pasteur de Tunis, Tunis, Tunisia.
Henda TouziLaboratory of Clinical Virology, Institute Pasteur de Tunis, Tunis, Tunisia.
Mohamed Msaddak AzouzDepartment of Gastroenterology, Hospital of Tahar Maamouri, Nabeul, Tunisia.
Nabyl Ben MamiDepartment of Gastroenterology, Hospital La Rabta, Tunis, Tunisia.
Henda TrikiLaboratory of Clinical Virology, Institute Pasteur de Tunis, Tunis, Tunisia.
Institut Pasteur de Tunis · TNHôpital La Rabta · TNHôpital Sahloul · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatitis B virus (HBV) infection is a public health problem in developing countries. HBV genotypes play major role in the evolution of infection since they were involved in different clinical presentations and response to treatment.

objectivesThis study was conducted to evaluate the efficiency of restriction fragment length polymorphism (RFLP) analysis for HBV genotyping. PATIENTS AND

methodsWe investigated 98 samples collected from patients chronically infected with HBV. HBV genotypes were determined by analysis of patterns obtained after amplification in Pre-S region and digestion of the amplicon by two endonucleases AvaII and DpnII. Obtained results were confirmed by partial sequencing in the same region.

resultsTwo different HBV genotypes were detected in this study, Genotype D (in 95. 9%) and Genotype A (in 4.1%). Seventy-four samples (75.5%) were successfully genotyped with RFLP analysis and all classified as genotype D. The remaining 24 samples (24.5%) which were un-genotyped by RFLP analysis, were classified by partial sequencing of the pre-S region as HBV genotype D (20 samples, 20.4%) and genotype A (4 samples, 4.1%). Atypical profiles were significantly associated with advanced liver disease (P = 0.001) as well as older age (P < 0.05).

conclusionsSeveral previous studies used PCR-RFLP to genotype HBV; however, we showed the high risk to obtain atypical profiles, especially in advanced stages of chronic infection, with as results difficulties to genotype the virus. These profiles resulted from the accumulation of mutations during natural course of infection resulting in a modification in restriction sites for enzymes. So, we recommended completing the investigation by partial sequencing to confirm obtained results.

Indexed as

Direct SequencingGenotypeHepatitis B VirusRestriction Fragment Length Polymorphism

Identifiers

PMID24348634
PMCPMC3842526
OpenAlexW2106455172

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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.