Association of single nucleotide polymorphisms in micro RNA s with susceptibility to hepatitis B virus infection and HBV ‐related liver complications: A study in a Saudi Arabian population
The aim of this study was to evaluate the association of 10 SNP s in different micro RNA s (mi RNA s) with susceptibility to hepatitis B virus ( HBV ) infection, HBV clearance, persistence of chronic HBV infection, and progression to liver cirrhosis and hepatocellular carcinoma ( HCC ). Patients wer...
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Veröffentlicht in: | Journal of viral hepatitis 2017-12, Vol.24 (12), p.1132-1142 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The aim of this study was to evaluate the association of 10
SNP
s in different micro
RNA
s (mi
RNA
s) with susceptibility to hepatitis B virus (
HBV
) infection,
HBV
clearance, persistence of chronic
HBV
infection, and progression to liver cirrhosis and hepatocellular carcinoma (
HCC
). Patients were categorized into the following groups: inactive
HBV
carrier, active
HBV
carrier,
HBV
‐cleared subject and cirrhosis+
HCC
. Samples were analysed for 10
SNP
s in micro
RNA
s using either
PCR
‐based genotyping or the TaqMan assay. We found that rs1358379 was associated with susceptibility to
HBV
infection,
HBV
clearance, persistent chronic
HBV
infection and liver cirrhosis+
HCC
. In addition, we found that rs2292832 and rs11614913 were associated with risk of
HBV
infection, viral clearance and cirrhosis+
HCC
, whereas rs2910164 was associated with proneness to
HBV
infection, and ability to clear the virus. There was evidence of associations between rs6505162 and
HBV
clearance and the development of liver disease, whereas a single association was found between rs2289030 and
HBV
clearance. Similarly, rs7372209 and rs4919510 were specifically associated with the development of
HBV
‐induced liver complications.
SNP
s in mi
RNA
s affect the susceptibility, clearance and progression of
HBV
infection in Saudi Arabian patients. We found, using Gene Ontology or pathway analyses, that these genes may contribute to the pathophysiology of
HBV
infection and related liver complications. However, differences in the association of examined
SNP
s with various clinical stages indicate variations in the respective functional roles of these polymorphisms and their mi
RNA
s, and thus, further investigation to fully explore their therapeutic potential is warranted. |
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ISSN: | 1352-0504 1365-2893 |
DOI: | 10.1111/jvh.12749 |