VDR polymorphisms influence the immune response in type 1 diabetic children from Santiago, Chile
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2007-07Metadata
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García, Diego
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VDR polymorphisms influence the immune response in type 1 diabetic children from Santiago, Chile
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Abstract
Objective: To evaluate the influence of ApaI, BsmI and TaqI polymorphisms of the VDR gene and HLA-DQB1* alleles in type 1
diabetic children and to assess their possible relationship with circulating levels of 25-hydroxyvitamin D3, auto-antibodies, and
INFg/TGFb1 cytokines levels in Chilean cases and controls.
Methods: DNA and serum samples from 216 newly diagnosed type 1 diabetic and 203 unrelated control children were evaluated for
IA-2 and GAD65 auto-antibodies, 25-hydroxyvitamin D3 levels, HLA-DQB1* alleles, and VDR gene polymorphisms.
Results: The frequency of the b allele and the bb genotype in type 1 diabetic patients was significantly lower compared with the
control group (0.635 versus 0.749, p < 0.01 and 0.370 versus 0.567, p < 0.04). 25-Hydroxyvitamin D3 levels showed no differences
between type 1 diabetic and healthy children. In cases, 25-hydroxyvitamin D3 levels were not associated with a special autoantibodies
profile according to the presence or absence of GAD65
+ or IA-2+. The haplotype combination BAT was higher in cases
(0.062 versus 0.019, p < 0.0022) and bAT was more frequent in controls (0.266 versus 0.180, p < 0.003). In cases, the aaBbTT
genotype showed the most significant increase in TGFb1 level across the VDR categories. Finally, when considering the HLA class
II risk genotype (DQB1*0302) and the VDR genotypes (AabbTT and aabbTT), higher levels of GAD65, IA-2 and TGFb1 were
observed among diabetic children.
Conclusion: We found an association between a VDR polymorphism (BsmI) and type 1 diabetes. An association was found of
AabbTT and aabbTT genotypes and the HLA-DQB1*0302 allele with high levels of GAD65, IA-2 and TGFb1.
Patrocinador
This work was supported by FONDECYT Grant
1030680 (Prof. Francisco Pe´rez-Bravo).
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DIABETES RESEARCH AND CLINICAL PRACTICE, v.: 77, issue: 1, p.: 134-140, JUL 2007
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