共 39 条
Gender-specific association of vitamin D receptor polymorphism combinations with type 1 diabetes mellitus
被引:79
作者:

Györffy, B
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机构: Semmelweis Univ, Dept Paediat 1, H-1085 Budapest, Hungary

Vásárhelyi, B
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机构: Semmelweis Univ, Dept Paediat 1, H-1085 Budapest, Hungary

Krikovszky, D
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机构: Semmelweis Univ, Dept Paediat 1, H-1085 Budapest, Hungary

Madácsy, L
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机构: Semmelweis Univ, Dept Paediat 1, H-1085 Budapest, Hungary

Tordai, A
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机构: Semmelweis Univ, Dept Paediat 1, H-1085 Budapest, Hungary

Tulassay, T
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机构: Semmelweis Univ, Dept Paediat 1, H-1085 Budapest, Hungary

Szabó, A
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机构: Semmelweis Univ, Dept Paediat 1, H-1085 Budapest, Hungary
机构:
[1] Semmelweis Univ, Dept Paediat 1, H-1085 Budapest, Hungary
[2] Hungarian Acad Sci, Res Lab Paediat & Nephrol, Budapest, Hungary
[3] Natl Med Ctr, Inst Haematol & Immunol, Budapest, Hungary
关键词:
D O I:
10.1530/eje.0.1470803
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
wObjective: Recent data have indicated the significance of vitamin D receptor (VDR) polymorphisms in type 1 diabetes mellitus (T1DM). We have studied the association of five known restriction enzyme polymorphisms of the VDR gene in patients with T1DM. Design and Methods: One hundred and seven children with T1DM (T1DM for 5 years; age, 1-14 years; boys/girls, 57/50; body mass index, 17.0 2.3kg/M 2; haemoglobin A,, 103 healthy subjects were enrolled. The VDR polymorphisms ApaI, BsmI, FokI, TaqI and Tru9I ('a', V, 'f', 't' and 'u' alleles respectively) were investigated. Results: The 't' and 'T' alleles miss the Hardy-Weinberg equilibrium (P < 0.01) in control and diabetic populations; we therefore excluded this polymorphism from further analysis. We did not find a difference in the allele prevalence in TIDM patients and controls of any of the five polymorphisms. However, when the 'b', 'a' and 'u' alleles were simultaneously compared in girls, there was a significantly higher prevalence in patients with diabetes compared with controls ('b' + 'a' + 'u' present/absent: healthy, 0/53; diabetic, 13/37; P < 0.005). In boys the prevalence of 'b'+'a'+'u' genotype was similar in T1DM and controls. Conclusions: The impact of the T allele cannot be investigated in this study population. Not a single VDR polymorphism increases the susceptibility to T1DM. The common presence of the 'b', 'a' and 'u' alleles greatly increases the probability of T1DM in girls.
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页码:803 / 808
页数:6
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