2018, Number 4
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Ann Hepatol 2018; 17 (4)
Relationship of Severity of Hepatitis A with Polymorphisms in Hepatitis A Virus Cellular Receptor 1 (HAVCR1) Gene
Benjamin M, Agnihotry S, Srivastava A, Bolia R, Yachha SK, Aggarwal R
Language: English
References: 28
Page: 561-568
PDF size: 221.36 Kb.
ABSTRACT
Introduction and aim. HAVCR1 protein is the cellular receptor for hepatitis A virus (HAV). Genetic polymorphism in this gene
may alter the outcome of HAV infection. In a previous study, a 6-amino acid insertion (157insMTTTVP) in
HAVCR1 gene was associated
with more severe disease. We decided to investigate this association further.
Material and methods. We sequenced exon
4 of the
HAVCR1 gene in patients with clinical hepatitis A attending our institution, and a group of healthy controls in a disease-endemic
setting in India. Frequencies of different haplotypes of a genomic region with two overlapping insertion-deletion polymorphisms
(indels; rs141023871 and rs139041445) were compared between patients and controls, as well as between patients with and without
a severe form of disease (liver failure).
Results. The gene had three haplotypes in the region of interest – a short form, an intermediate-
form with a 5-amino acid 157insMTTVP insertion and a long-form with a 6-amino acid 157insMTTTVP insertion. The allele frequency
(29/150 [19%]
vs. 43/146 [29%]; p = ns) and haplotype frequency (29/75 [39%]
vs. 39/73 [53%]; p = ns) of the
157insMTTTVP variant were similar in hepatitis A patients and healthy controls (30%). Further, the allele frequency (12/58 [21%]
vs.
17/92 [18%]; p = ns) and haplotype frequency (12/29 [41%]
vs.17/46 [37%]; p = ns) of the longest variant were also similar in patients
with severe and mild disease.
Discussion. In the study population, the 157insMTTTVP variant of
HAVCR1 gene was not
associated with more severe outcome of HAV infection. Further studies in other populations around the world are needed to assess
the relation of this genetic variation with disease outcome.
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