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Haplotype combination of Calpain-10 gene polymorphism is associated with metabolic syndrome in type 2 diabetes
Patients with metabolic syndrome are at increased risk of developing cardiovascular disease. The combinations of the haplotype created by the alleles of three single nucleotide polymorphisms (SNPs): SNP-43, -19, and -63 of the Calpain-10 gene ( CAPN10), have been reported to be associated with the r...
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Published in: | Diabetes research and clinical practice 2006-09, Vol.73 (3), p.268-275 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Patients with metabolic syndrome are at increased risk of developing cardiovascular disease. The combinations of the haplotype created by the alleles of three single nucleotide polymorphisms (SNPs): SNP-43, -19, and -63 of the Calpain-10 gene (
CAPN10), have been reported to be associated with the risk of type 2 diabetes in many populations. The aim of this study was to examine the association of the
CAPN10 polymorphism with metabolic syndrome in patients with type 2 diabetes in Korea. Overall, 382 patients with type 2 diabetes were enrolled in this study. All the subjects were genotyped according to
CAPN10 SNP-43, -19, and -63. The restriction fragment length polymorphism method was used for the three SNPs. The baseline presence of components of metabolic syndrome was determined. Two hundred and sixty-five (69.4%) patients had metabolic syndrome. Patients with the 111/121 haplotype combination showed a higher risk of hypertension than the other haplotype combinations (odd ratio (OR)
=
2.334,
P
=
0.010). Patients with the 111/121 haplotype combination had a significantly high risk of metabolic syndrome (OR
=
1.927,
P
=
0.042). The results of this study suggest that a novel 111/121 haplotype combination created by the
CAPN10 SNP-43, -19, and -63 increases the susceptibility to the metabolic syndrome in patients with type 2 diabetes. |
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ISSN: | 0168-8227 1872-8227 |
DOI: | 10.1016/j.diabres.2006.01.011 |