Tian Yingjie, Xiang Xuesong, Ying Xiaoming, Li Dongyun, Zhao Jiajia, Zhang Zechen, Li Qingxia
Hangzhou Ubao Healthcare Technology Co. , Ltd, Hangzhou 311121, China.
National Institute for Nutrition and Health, China CDC, Beijing 100050, China.
Wei Sheng Yan Jiu. 2020 Nov;49(6):927-931. doi: 10.19813/j.cnki.weishengyanjiu.2020.06.009.
To investigate the relationship between vitamin D binding protein gene rs2282679 A/C polymorphism with blood vitamin D levels.
A total of 286 eligible subjects were selected from one university in Hebei Province. Serum 25-hydroxylated vitamin D levels were measured by liquid chromatography-mass spectrometry, and gene chip was used for genotyping of rs2282679 locus. Statistical analysis was performed using R software.
A total of 285 participants in the study completed the experiment, and result indicated that the distribution of the rs2282679 locus A/C polymorphism in the participants was consistent with the Hardy-Weinberg equilibrium. The genotype of rs2282679 was significantly associated with serum vitamin D insufficiency and deficiency(P=0. 031). Allele A was a risk factor for vitamin D insufficiency and deficiency. The OR value of allele C relative to A was 0. 65, and the genetic pattern of allele C relative to A was dominant(P=0. 03).
The vitamin D-binding protein gene rs2282679 was significantly associated with serum vitamin D insufficiency and deficiency in college students, and A-allele is a risk factor accounting for vitamin D insufficiency and deficiency in college students.
探讨维生素D结合蛋白基因rs2282679 A/C多态性与血液维生素D水平之间的关系。
从河北省某高校选取286名符合条件的受试者。采用液相色谱-质谱法测定血清25-羟基维生素D水平,并用基因芯片对rs2282679位点进行基因分型。使用R软件进行统计分析。
共有285名研究参与者完成了实验,结果表明rs2282679位点A/C多态性在参与者中的分布符合哈迪-温伯格平衡。rs2282679的基因型与血清维生素D不足和缺乏显著相关(P = 0.031)。等位基因A是维生素D不足和缺乏的危险因素。等位基因C相对于A的OR值为0.65,等位基因C相对于A的遗传模式为显性(P = 0.03)。
维生素D结合蛋白基因rs2282679与大学生血清维生素D不足和缺乏显著相关,A等位基因是导致大学生维生素D不足和缺乏的危险因素。