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Association of vitamin D receptor TaqI and ApaI genetic polymorphisms with nephrolithiasis and end stage renal disease: a meta-analysis.
Hussain, Tajamul; Naushad, Shaik M; Ahmed, Anwar; Alamery, Salman; Mohammed, Arif A; Abdelkader, Mohamed O; Alkhrm, Nasser Abobakr Nasser.
Afiliação
  • Hussain T; Center of Excellence in Biotechnology Research, Department of Biochemistry, College of Science Building 5, King Saud University, Riyadh, 11451, Saudi Arabia. thussain@ksu.edu.sa.
  • Naushad SM; Biochemical Genetics, Sandor Life Sciences Pvt. Ltd, Hyderabad, India.
  • Ahmed A; Center of Excellence in Biotechnology Research, Department of Biochemistry, College of Science Building 5, King Saud University, Riyadh, 11451, Saudi Arabia.
  • Alamery S; Center of Excellence in Biotechnology Research, Department of Biochemistry, College of Science Building 5, King Saud University, Riyadh, 11451, Saudi Arabia.
  • Mohammed AA; Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
  • Abdelkader MO; Center of Excellence in Biotechnology Research, Department of Biochemistry, College of Science Building 5, King Saud University, Riyadh, 11451, Saudi Arabia.
  • Alkhrm NAN; Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
BMC Med Genet ; 20(1): 193, 2019 12 10.
Article em En | MEDLINE | ID: mdl-31822280
ABSTRACT

BACKGROUND:

The deficiency of vitamin D receptor (VDR) or its ligand, vitamin D3, is linked to the development of renal diseases. The TaqI (rs731236) and ApaI (rs7975232) polymorphisms of VDR gene are widely studied for their association with renal disease risk. However, studies have largely been ambiguous.

METHODS:

Meta-analysis was carried out to clarify the association of TaqI (2777 cases and 3522 controls) and ApaI (2440 cases and 3279 controls) polymorphisms with nephrolithiasis (NL), diabetic nephropathy (DN) and end stage renal disease (ESRD).

RESULTS:

The VDR TaqI C-allele under allele contrast was significantly associated with ESRD in both fixed effect and random effect models, and ApaI C-allele with ESRD only under fixed effect model. Cochrane Q-test showed no evidence of heterogeneity for TaqI polymorphism and a significant heterogeneity for Apa I polymorphism. No publication bias was observed for both the polymorphisms.

CONCLUSIONS:

The present meta-analysis identifies TaqI and ApaI polymorphisms of VDR gene as risk factors for renal diseases.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Desoxirribonucleases de Sítio Específico do Tipo II / Receptores de Calcitriol / Polimorfismo de Nucleotídeo Único / Nefropatias Diabéticas / Nefrolitíase / Falência Renal Crônica Idioma: En Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Arábia Saudita

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Desoxirribonucleases de Sítio Específico do Tipo II / Receptores de Calcitriol / Polimorfismo de Nucleotídeo Único / Nefropatias Diabéticas / Nefrolitíase / Falência Renal Crônica Idioma: En Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Arábia Saudita