Evidence map›Paper›PMID 30766578›Full record

ArticleAfrican health sciences2018

Genetic diversity of hepatitis B co-infection with hepatitis C, D and E viruses among Malaysian chronic hepatitis B patients.

Shuaibu Abdullahi Hudu, Mohd Taib Niazlin, Syafinaz Amin Nordin, Soek Siam Tan, Haniza Omar, Hamiza Shahar, Noor Aliza Mutalib, Zamberi Sekawi

Open access · diamondAbstract read
In one paragraph

Article in African health sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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

8 authors at 1 institution in 1 country.

Shuaibu Abdullahi HuduDepartment of Medical Microbiology and Parasitology, Faculty of Basic Medical Sciences, College of Health Sciences, Usmanu Danfodiyo University Sokoto, 840232 Sokoto State, Nigeria.
Mohd Taib NiazlinDepartment of Medical Microbiology and Parasitology, Faculty of Medicine and Health Sciences, University Putra Malaysia.
Syafinaz Amin NordinDepartment of Medical Microbiology and Parasitology, Faculty of Medicine and Health Sciences, University Putra Malaysia.
Soek Siam TanDepartment of Hepatology, Selayang Hospital, Lebuh Selayang Batu Cave Selangor, Malaysia.
Haniza OmarDepartment of Hepatology, Selayang Hospital, Lebuh Selayang Batu Cave Selangor, Malaysia.
Hamiza ShaharDepartment of Hepatology, Selayang Hospital, Lebuh Selayang Batu Cave Selangor, Malaysia.
Noor Aliza MutalibDepartment of Hepatology, Selayang Hospital, Lebuh Selayang Batu Cave Selangor, Malaysia.
Zamberi SekawiDepartment of Medical Microbiology and Parasitology, Faculty of Medicine and Health Sciences, University Putra Malaysia.
Ministry of Health · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatitis B virus co-infection with other strains of viral hepatitis is associated with increased risk of liver cirrhosis and hepatic decompensation.

objectivesThis is a prevalence study that assessed the genetic diversity of chronic hepatitis B patients and coinfection.

methodsChronic hepatitis B patients enrolled in this study were tested for antibodies of other hepatitis viruses using ELISA kits. Patient clinical profiles were collected and partial genes of HBV, HCV, and HEV were amplified, sequenced, and analyzed using phylogenetic analysis. The associations between variables were determined using the chi-squared test.

resultsOf the 82 patients recruited for this study, 53.7% were non-cirrhotic, 22.0% cirrhotic, 20.7% acute flare and 3.7% hepatocellular carcinoma. Majority (58%) of patients had a high level of ALT (≥34 U/L). Sequence analysis showed HBV (63.9%) belonged to genotype B, HEV belonged to genotype 4 while HCV belonged to genotype 3a and the genotypes were found to be significantly associated with the clinical stage of the patients (χ2=56.632; p<0.01). Similarly, Hepatitis B e antigen was also found to be significantly associated with the clinical stage of infection (χ2=51.952; p<0.01).

conclusionThis study revealed that genetic diversity was found to have a significant impact on the severity of infection.

Indexed as

AdultAntibodies, ViralCarcinoma, HepatocellularCross-Sectional StudiesDNA, ViralFemaleGenetic VariationGenotypeHepatitis B, ChronicHepatitis CHepatitis DHepatitis EHumansLiver CirrhosisLiver Function TestsLiver NeoplasmsAntibodies, ViralDNA, ViralRNA, ViralHepatitis co-infectionHepatitis genetic diversityMalaysia

Identifiers

PMID30766578
PMCPMC6354894
OpenAlexW2902807892

What OpenQuestion holds

Textmetadata
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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.