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Susceptibility and progression of end stage renal disease are not associated with angiotensin II type 1 receptor gene polymorphism.
Hanna, Mariam Onsy F; Shahin, Rasha Mohamad Hosny; Meshaal, Safa S; Kostandi, Inas F.
Afiliação
  • Hanna MO; a Department of Clinical Pathology and.
  • Shahin RM; a Department of Clinical Pathology and.
  • Meshaal SS; a Department of Clinical Pathology and.
  • Kostandi IF; b Department of Internal Medicine , Faculty of Medicine, Cairo University , Kasr Al Ainy , Cairo , Egypt.
J Recept Signal Transduct Res ; 35(5): 381-5, 2015.
Article em En | MEDLINE | ID: mdl-25316403
ABSTRACT
CONTEXT The role of the angiotensin II type 1 receptor (AT1R) gene polymorphism, A1166C, has been shown to be associated with end stage renal disease (ESRD) and its progression. There is also some evidence that HLA class II alleles are associated with ESRD independent of other factors.

OBJECTIVE:

To examine the association between AT1R gene polymorphism in the susceptibility and progression to ESRD in patients with chronic renal failure and to investigate if the AT1R genotypes and HLA-DR alleles predict the time to ESRD. MATERIALS AND

METHODS:

Genotyping was performed in 50 ESRD patients and 44 control subjects for the AT1R A1166C gene polymorphism using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). ESRD patients were examined for HLA-DRB1 alleles according to a reverse hybridization line probe assay.

RESULTS:

Allele and genotype frequencies of the AT1R polymorphism did not differ significantly between ESRD patients and controls. Furthermore, there was no association between the AT1R gene polymorphism or HLA-DRB1 alleles with the time to the occurrence of end stage failure. DISCUSSION AND

CONCLUSION:

We concluded that the AT1R genotype does not contribute to the genetic susceptibility of ESRD and is not associated with progression of chronic kidney failure to ESRD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Receptor Tipo 1 de Angiotensina / Falência Renal Crônica Tipo de estudo: Diagnostic_studies / Etiology_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País como assunto: Africa Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Receptor Tipo 1 de Angiotensina / Falência Renal Crônica Tipo de estudo: Diagnostic_studies / Etiology_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País como assunto: Africa Idioma: En Ano de publicação: 2015 Tipo de documento: Article