[中国育龄妇女维生素D基因多态性与血清25-羟基维生素D的关系]。

Xiaoyun Shan, Xiayu Zhao, Siran Li, Yichun Hu, Lichen Yang
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引用次数: 0

摘要

目的:分析维生素D(VitD)相关单核苷酸多态性(SNP)与25-羟基维生素D(25(OH) D)水平与维生素D营养状况的关系。方法:选取“2015年中国成人慢性病与营养监测”样本库中18-45岁育龄妇女1507名。收集受试者的基本信息(包括地区、季节、年龄、身高、体重等)。筛选与VitD代谢相关的SNP,采用改进的多重连接酶检测反应进行SNP检测。采用液相色谱串联质谱法测定血清25(OH)D浓度。采用广义线性模型和二元logistic回归模型分析不同基因型对25(OH)D水平和维生素D缺乏的影响。结果:经纬度、地域、地域类型、季节、年龄等因素调整后,CYP2R1 rs12794714、GC rs2282679、GC rs7041、VDR rs2228570与育龄妇女血清25(OH)D水平相关。携带GG基因型rs2282679的个体VitD缺乏风险显著高于携带TT基因型个体(OR=2.466, 95%CI 1.690 ~ 3.598, P<0.001),携带A基因型rs2228570的个体VitD缺乏风险显著低于携带G基因型个体(OR_(AA)=0.625, 95%CI 0.446 ~ 0.876, P_(AA)=0.006;携带OR_(GA)=0.661, 95%CI 0.502 ~ 0.869, P_(GA)=0.003)。结论:CYP2R1 rs12794714、GC rs2282679、GC rs7041和VDR rs2228570基因型分布可能与中国育龄妇女血清25(OH)D水平或维生素D营养状况有关。
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[Association of vitamin D gene polymorphisms and serum 25-hydroxyvitamin D in Chinese women of childbearing age].

Objective: To analyze the relationship between vitamin D(VitD)-related single nucleotide polymorphism(SNP) and 25-hydroxyvitamin D(25(OH) D) levels and VitD nutritional status.

Methods: A total of 1507 women of childbearing age aged 18-45 were selected from the sample bank of "2015 Chinese adult chronic disease and nutrition monitoring". Basic information(including region, season, age, height, weight, etc. ) of the subjects was collected. The SNPs related to VitD metabolism were screened, and the improved multiple ligase detection reaction was used for SNP testing. Liquid chromatography tandem mass spectrometry was used to determine the serum 25(OH)D concentration. The effects of genotypes on 25(OH)D level and VitD deficiency were analyzed by generalized linear model and binary logistic regression model, respectively.

Results: After adjusting for latitude, region, region type, season and age, CYP2R1 rs12794714, GC rs2282679, GC rs7041 and VDR rs2228570 were associated with serum 25(OH)D levels in women of childbearing age. The risk of VitD deficiency in individuals carrying GG genotype at rs2282679 was significantly higher than that in individuals carrying TT genotype(OR=2.466, 95%CI 1.690-3.598, P<0.001), and the risk of VitD deficiency in individuals carrying A allele at rs2228570 was lower than that in individuals carrying G allele(OR_(AA)=0.625, 95%CI 0.446-0.876, P_(AA)=0.006;OR_(GA)=0.661, 95%CI 0.502-0.869, P_(GA)=0.003).

Conclusion: The genotype distribution of CYP2R1 rs12794714, GC rs2282679, GC rs7041 and VDR rs2228570 may be related to serum 25(OH)D level or VitD nutritional status of Chinese women of childbearing age.

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