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Vitamin D receptor gene polymorphisms and type 1 diabetes mellitus in a Korean population.
Cheon, Chong-Kun; Nam, Hyo-Kyoung; Lee, Kee-Hyoung; Kim, Su Yung; Song, Ji Sun; Kim, Choongrak.
Affiliation
  • Cheon CK; Department of Pediatrics, Pediatric Endocrinology, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan.
  • Nam HK; Department of Pediatrics, College of Medicine, Korea University, Seoul.
  • Lee KH; Department of Pediatrics, College of Medicine, Korea University, Seoul.
  • Kim SY; Department of Pediatrics, Pediatric Endocrinology, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan.
  • Song JS; Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Gyeongnam.
  • Kim C; Department of Statistics, Pusan National University, Pusan, South Korea.
Pediatr Int ; 57(5): 870-4, 2015 Oct.
Article de En | MEDLINE | ID: mdl-25808747
ABSTRACT

BACKGROUND:

Vitamin D receptor (VDR) has been suggested to play a role in the pathogenesis of type 1 diabetes mellitus (T1DM). There has been no case-control study examining the association between VDR polymorphisms and T1DM among Korean subjects with a low incidence of T1DM.

METHODS:

Eighty-one T1DM patients and 113 unrelated healthy controls with no history of DM or other autoimmune diseases were investigated at either Pusan National University Children's Hospital or Korea University Anam Hospital between March 2009 and September 2013. Polymerase chain reaction-restriction fragment length polymorphism was utilized to genotype single nucleotide substitutions at TaqI, BsmI, and ApaI alleles.

RESULTS:

All frequencies in T1DM and control subjects were in Hardy-Weinberg equilibrium, although ApaI in controls and TaqI in T1DM showed relatively weak equilibrium. TaqI and BsmI differences were significant (P = 0.045 and P = 0.012, respectively) after applying Bonferroni correction. The TT genotype carrier frequency among controls was higher than among the T1DM patients (P = 0.015; OR, 2.98; 95%CI 1.19-7.42). T allele frequency was higher among controls than T1DM patients (P = 0.019; OR, 2.78; 95%CI 1.15-6.72). The frequency of bb genotype carriers among controls was higher than among T1DM patients (P = 0.004; OR, 4.13; 95%CI 1.4-12.10). The frequency of the b allele among controls was higher than that among T1DM patients (P = 0.016; OR, 3.20; 95%CI 1.19-8.60).

CONCLUSIONS:

T and b TaqI and BsmI alleles are protective against T1DM in Korean subjects.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Polymorphisme génétique / ADN / Récepteur calcitriol / Prédisposition génétique à une maladie / Diabète de type 1 Type d'étude: Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Child / Female / Humans / Male Pays/Région comme sujet: Asia Langue: En Journal: Pediatr Int Sujet du journal: PEDIATRIA Année: 2015 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Polymorphisme génétique / ADN / Récepteur calcitriol / Prédisposition génétique à une maladie / Diabète de type 1 Type d'étude: Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Child / Female / Humans / Male Pays/Région comme sujet: Asia Langue: En Journal: Pediatr Int Sujet du journal: PEDIATRIA Année: 2015 Type de document: Article