Your browser doesn't support javascript.
loading
Calpain-10 and Adiponectin Gene Polymorphisms in Korean Type 2 Diabetes Patients
Article in En | WPRIM | ID: wpr-716968
Responsible library: WPRO
ABSTRACT

BACKGROUND:

Genetic variations in calpain-10 and adiponectin gene are known to influence insulin secretion and resistance in type 2 diabetes mellitus. Recently, several single nucleotide polymorphisms (SNPs) in calpain-10 and adiponectin gene have been reported to be associated with type 2 diabetes and various metabolic derangements. We investigated the associations between specific calpain-10 and adiponectin gene polymorphisms and Korean type 2 diabetes patients.

METHODS:

Overall, 249 type 2 diabetes patients and 131 non-diabetic control subjects were enrolled in this study. All the subjects were genotyped for SNP-43 and -63 of calpain-10 gene and G276T and T45G frequencies of the adiponectin gene. The clinical characteristics and measure of glucose metabolism were compared within these genotypes.

RESULTS:

Among calpain-10 polymorphisms, SNP-63 T/T were more frequent in diabetes patients, and single SNP-63 increases the susceptibility to type 2 diabetes. However, SNP-43 in calpain-10 and T45G and intron G276T in adiponectin gene were not significantly associated with diabetes, insulin resistance, nor insulin secretion.

CONCLUSION:

Variations in calpain-10, SNP-63 seems to increase the susceptibility to type 2 diabetes in Koreans while SNP-43 and adiponectin SNP-45, -276 are not associated with impaired glucose metabolism.
Subject(s)
Key words
Full text: 1 Index: WPRIM Main subject: Genetic Variation / Insulin Resistance / Introns / Polymorphism, Single Nucleotide / Diabetes Mellitus, Type 2 / Adiponectin / Genotype / Glucose / Insulin / Metabolism Limits: Humans Language: En Journal: Endocrinology and Metabolism Year: 2018 Type: Article
Full text: 1 Index: WPRIM Main subject: Genetic Variation / Insulin Resistance / Introns / Polymorphism, Single Nucleotide / Diabetes Mellitus, Type 2 / Adiponectin / Genotype / Glucose / Insulin / Metabolism Limits: Humans Language: En Journal: Endocrinology and Metabolism Year: 2018 Type: Article