Your browser doesn't support javascript.
loading
Association of rs2282679 A/C polymorphism in vitamin D binding protein gene with vitamin D deficiency / 中华内分泌代谢杂志
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-442884
Responsible library: WPRO
ABSTRACT
[Summary] To investigate the association of rs2282679 A/C polymorphism in vitamin D binding protein gene with vitamin D deficiency in 1 216 participants.A standardized questionnaire was applied to collect information on alcohol consumption,smoking habits,and use of medications.Serum 25-hydroxyvitamin D [25 (OH) D] was determined by radioimmunoassay.Vitamin D binding protein genotypes were determined by SNaPshot method.1216participants included 457 women(37.6%),478 (39.3%)with vitamin D deficiency [25 (OH) D<50 nmol/L],and 386 (31.7%) overweight/obese participants.The frequencies of rs2282679 CC,AC,and AA genotypes were 8.7%,41.0%,and 50.3%,respectively.The distributions of genotypes and alleles differed significantly between participants with sufficient vitamin D and those with vitamin D deficiency (P < 0.05).There were significant differences in the serum levels of 25 (OH) D between three genotypes before and after being adjusted for covariates (P<0.01).AA had a 22% (OR =0.78,95% CI 0.65-0.93,P =0.006) lowered risk of vitamin D deficiency compared with the whole studied population.Compared with CC genotype,AA had a 36% lowered risk of vitamin D deficiency(OR =0.64,95 % CI 0.42-0.98,P =0.006),while there was no significant difference between AC and CC genotypes(OR=0.87,95% CI0.57-1.34,P=0.53).In conclusion,the vitamin D binding protein rs2282679A/C polymorphism was significantly associated with serum level of 25 (OH) D and risk of vitamin D deficiency.

Full text: Available Database: WPRIM (Western Pacific) Language: Chinese Journal: Chinese Journal of Endocrinology and Metabolism Year: 2013 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Language: Chinese Journal: Chinese Journal of Endocrinology and Metabolism Year: 2013 Document type: Article
...