NAN NWE WIN

NAN NWE WIN

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Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 December 2017 in Diseases
Verified
Journal Article
Open access
PDF file
NWNAN NWE WIN
NAN NWE WIN
Shingo NakamotoShingo Nakamoto
Shingo Nakamoto
MSMyint Sein
Myint Sein
MMMitsuhiko Moriyama
Mitsuhiko Moriyama
Tatsuo KandaTatsuo Kanda
Tatsuo Kanda
HSHiroshi Shirasawa
Hiroshi Shirasawa
Myanmar is adjacent to India, Bangladesh, Thailand, Laos and China. In Myanmar, the prevalence of hepatitis B virus (HBV) infections is 6.5% and accounts for 60% of hepatocellular carcinoma. HBV has nine genotypes that have been identified by molecular genetic analysis. HBV genotypes are associated with several clinical features. We reviewed the prevalence of HBV genotypes in Myanmar and neighboring countries. We also reviewed HBV genotypes in refugees from Myanmar. HBV subgenotype C1 is predominant in Myanmar. As HBV genotype C is associated with hepatocellular carcinoma (HCC), it is important to screen for cirrhosis and HCC and to prevent their development in HBV-infected individuals of Myanmar.

Verified
Journal Article
Open access
PDF file
NWNAN NWE WIN
NAN NWE WIN
SNShingo Nakamoto
Shingo Nakamoto
Tatsuo KandaTatsuo Kanda
Tatsuo Kanda
HTHiroki Takahashi
Hiroki Takahashi
ATAzusa Takahashi-Nakaguchi
Azusa Takahashi-Nakaguchi
HSHiroshi Shirasawa
Hiroshi Shirasawa
Determination of hepatitis C virus (HCV) genotypes plays an important role in the direct-acting agent era. Discrepancies between HCV genotyping and serotyping assays are occasionally observed. Eighteen samples with discrepant results between genotyping and serotyping methods were analyzed. HCV serotyping and genotyping were based on the HCV nonstructural 4 (NS4) region and 5′-untranslated region (5′-UTR), respectively. HCV core and NS4 regions were chosen to be sequenced and were compared with the genotyping and serotyping results. Deep sequencing was also performed for the corresponding HCV NS4 regions. Seventeen out of 18 discrepant samples could be sequenced by the Sanger method. Both HCV core and NS4 sequences were concordant with that of genotyping in the 5′-UTR in all 17 samples. In cloning analysis of the HCV NS4 region, there were several amino acid variations, but each sequence was much closer to the peptide with the same genotype. Deep sequencing revealed that minor clones with different subgenotypes existed in two of the 17 samples. Genotyping by genome amplification showed high consistency, while several false reactions were detected by serotyping. The deep sequencing method also provides accurate genotyping results and may be useful for analyzing discrepant cases. HCV genotyping should be correctly determined before antiviral treatment.