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Effect of HLA-DPA1 alleles on chronic hepatitis B prognosis and treatment response.
Katrinli, Seyma; Enc, Feruze Yilmaz; Ozdil, Kamil; Ozturk, Oguzhan; Tuncer, Ilyas; Doganay, Gizem Dinler; Doganay, Levent.
Afiliación
  • Katrinli S; Department of Molecular Biology and Genetics, Istanbul Technical University, Istanbul, Turkey.
  • Enc FY; Department of Gastroenterology, Goztepe Training and Research Hospital, Medeniyet University, Istanbul, Turkey.
  • Ozdil K; Department of Gastroenterology, Umraniye Training and Research Hospital, University of Medical Sciences, Istanbul, Turkey.
  • Ozturk O; Department of Gastroenterology, Umraniye Training and Research Hospital, University of Medical Sciences, Istanbul, Turkey.
  • Tuncer I; Department of Gastroenterology, Goztepe Training and Research Hospital, Medeniyet University, Istanbul, Turkey.
  • Doganay GD; Department of Molecular Biology and Genetics, Istanbul Technical University, Istanbul, Turkey.
  • Doganay L; Department of Gastroenterology, Umraniye Training and Research Hospital, University of Medical Sciences, Istanbul, Turkey.
North Clin Istanb ; 3(3): 168-174, 2016.
Article en En | MEDLINE | ID: mdl-28275747
OBJECTIVE: Chronic hepatitis B (CHB) is a major health problem. The outcome of hepatitis B virus (HBV) infection is associated with variations in HLA-DPA1 alleles. The aim of this study was to investigate possible associations of HLA-DPA1 alleles with treatment response and with hepatitis B virus e antigen (HBeAg) seroconversion. METHODS: Eight different HLA-DPA1 alleles from 246 CHB patients were genotyped by polymerase chain reaction with sequence-specific primers at high resolution to investigate the association of HLA-DPA1 alleles with treatment response, development of cirrhosis, HBeAg seroconversion, and disease reoccurrence upon HBeAg loss. RESULTS: There was no significant association between HLA-DPA1 alleles and treatment response, development of cirrhosis, or HBeAg seroconversion. However, HLA-DPA1*04:01 allele was significantly more frequently found in patients who redeveloped disease upon HBeAg seroconversion (100% vs 36.8%: p=0.037; Fisher's exact test). CONCLUSION: HLA-DPA1*04:01 allele may be a risk factor for reoccurrence of CHB after HBeAg seroconversion.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: North Clin Istanb Año: 2016 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: North Clin Istanb Año: 2016 Tipo del documento: Article País de afiliación: Turquía
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