Relationship Between Hemochromatosis Gene Mutations and Degree of Fibrosis in Liver Disease Associated with Chronic Hepatitis B and C.

Objective: There are various factors that affect the degree of liver fibrosis in chronic viral hepatitis (CVH). Deposition of iron in the liver is one of these factors. Although hemochromatosis gene (HFE) mutation is determined as heterozygote, it is thought that it causes deposition of iron in the...

Descripción completa

Detalles Bibliográficos
Publicado en:Turkiye Klinikleri Journal of Medical Sciences Vol. 32; no. 4; pp. 917 - 925
Autores principales: Bagir, Gülay Simsek, Dogan, Ümit Bilge, Egesel, Türker, Canataroglu, Abdullah
Formato: research tables/charts Journal Article
Publicado: Turkiye Klinikleri Aug2012
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=104415875&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 104415875
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        13000292
        1VOP
      jtl: Turkiye Klinikleri Journal of Medical Sciences
      issn: 13000292
      maglogo: N
    pubinfo:
      dt: Aug2012
      vid: 32
      iid: 4
      pid: 67298
      pub: Turkiye Klinikleri
    artinfo:
      ui:
        104415875
        2011681416
        10.5336/medsci.2011-24436
        104415875
      ppf: 917
      ppct: 8
      formats:
        fmt:
          @attributes:
            type: P
      tig:
        atl: Relationship Between Hemochromatosis Gene Mutations and Degree of Fibrosis in Liver Disease Associated with Chronic Hepatitis B and C.
      aug:
        au:
          Bagir, Gülay Simsek
          Dogan, Ümit Bilge
          Egesel, Türker
          Canataroglu, Abdullah
        affil: Clinic of Internal Medicine, Adana Numune Training and Research Hospital, Adana
      sug:
        subj:
          Chronic Disease
          Fibrosis Risk Factors
          Genes
          Hemochromatosis Familial and Genetic
          Hepatitis B Complications
          Hepatitis C Complications
          Mutation
          Adolescence
          Adult
          Aged
          Aged, 80 and Over
          Alanine Aminotransferase Blood
          Aspartate Aminotransferase Blood
          Case Control Studies
          Data Analysis Software
          Descriptive Statistics
          Female
          Ferritin Blood
          Human
          Iron Blood
          Kruskal-Wallis Test
          Male
          Mann-Whitney U Test
          Middle Age
          One-Way Analysis of Variance
          Pearson's Correlation Coefficient
          T-Tests
          Transferrin Blood
          Adolescent: 13-18 years
          Adult: 19-44 years
          Aged: 65+ years
          Aged, 80 & over
          Middle Aged: 45-64 years
          Female
          Male
      ab: Objective: There are various factors that affect the degree of liver fibrosis in chronic viral hepatitis (CVH). Deposition of iron in the liver is one of these factors. Although hemochromatosis gene (HFE) mutation is determined as heterozygote, it is thought that it causes deposition of iron in the liver. However, the effect of the deposition of iron as a result of HFE gene mutation that leads to the progression of fibrosis in patients with CVH is still uncertain. The purpose of this study is to evaluate the association of HFE gene mutations with serum iron indices and degree of fibrosis in patients with CVH. Material and Methods: The study enrolled 83 patients with chronic hepatitis B, 61 patients with chronic hepatitis C and 50 healthy controls. Fifty-two of the patients also had cirrhosis. AST, ALT, serum iron, ferritin and transferrin saturations were measured and the presence of HFE mutations were investigated for all individuals. Liver biopsy was performed to all patients. Histopathological findings in the liver were scored as necroinflammatory activity and fibrosis according to the Knodell scoring scale. Results: The C282Y mutations could not be detected in any individuals. H63D heterozygous and homozygous mutations were found but they did not differ between patients (n=29, 20.1%) and controls (n=14, 28%). Presence of H63D mutations was not associated with serum iron indices or the degree of hepatic fibrosis. Conclusion:Our results showed that H63D gene mutations do not have a significant role in the progression of fibrosis in CVH.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: Turkish
    refInfo:
    holdings:
      @attributes:
        islocal: N