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维生素 D 结合蛋白基因变异与中国南方人群血清 25-羟维生素 D 和维生素 D 不足相关。

Genetic variant in vitamin D binding protein is associated with serum 25-hydroxyvitamin D and vitamin D insufficiency in southern Chinese.

机构信息

1] Department of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong, China [2] Centre for Genomic Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong, China [3] Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong, China.

出版信息

J Hum Genet. 2013 Nov;58(11):749-51. doi: 10.1038/jhg.2013.84. Epub 2013 Aug 8.

Abstract

Previous large-scale genome-wide meta-analysis identified four loci affecting 25-hydroxyvitamin D (25(OH)D) concentrations. However, whether these loci are associated with 25(OH)D concentration in southern Chinese remain unknown. Our primary aim was to examine whether the four top hits (rs2282679, rs10741657, rs12785878 and rs6013897) could be replicated in 712 southern Chinese women. The associations between these single-nucleotide polymorphisms (SNPs), serum 25(OH)D concentration (continuous variable) and vitamin D insufficiency (dichotomized variable) were examined using multivariable linear regression and logistic regression, respectively. Age, body mass index and season were adjusted in the model. Among these four SNPs, rs2282679 was associated with serum 25(OH)D levels (β=-0.066; P=9 × 10(-5)) and vitamin D insufficiency (odds ratio (OR)=1.51, 95% confidence interval (CI) 1.19-1.93; P=8.6 × 10(-4)), whereas rs12785878 was nominally associated with vitamin D insufficiency only (OR=0.79, 95% CI 0.63-0.99; P=0.042). Genotype risk score (GRS), by summing risk variants of these two SNPs, had more significant association with vitamin D insufficiency (OR=1.38; 95% CI 1.17-1.64; P(trend)=1.76 × 10(-4)) than the model that included only either SNP. The areas under receiver operating characteristic curves of rs2282679 and GRS were 0.561 (P=0.005) and 0.576 (P=5 × 10(-4)), respectively. Our study provides an independent evidence of the associations of rs2282679 and probably rs12785878 with 25(OH)D and vitamin D insufficiency in southern Chinese.

摘要

先前的大规模全基因组荟萃分析确定了四个影响 25-羟维生素 D(25(OH)D)浓度的基因座。然而,这些基因座是否与中国南方人群的 25(OH)D 浓度有关尚不清楚。我们的主要目的是检验这四个最强关联(rs2282679、rs10741657、rs12785878 和 rs6013897)在 712 名中国南方女性中是否可以被复制。使用多变量线性回归和逻辑回归分别检验这些单核苷酸多态性(SNP)与血清 25(OH)D 浓度(连续变量)和维生素 D 不足(二分类变量)之间的关联。在模型中调整了年龄、体重指数和季节。在这四个 SNP 中,rs2282679 与血清 25(OH)D 水平(β=-0.066;P=9×10(-5))和维生素 D 不足(比值比(OR)=1.51,95%置信区间(CI)1.19-1.93;P=8.6×10(-4))有关,而 rs12785878 仅与维生素 D 不足呈名义相关(OR=0.79,95%CI 0.63-0.99;P=0.042)。通过将这两个 SNP 的风险变异相加得到的基因型风险评分(GRS)与维生素 D 不足的关联更为显著(OR=1.38;95%CI 1.17-1.64;P(trend)=1.76×10(-4)),而不仅仅包含单个 SNP 的模型则没有。rs2282679 和 GRS 的受试者工作特征曲线下面积分别为 0.561(P=0.005)和 0.576(P=5×10(-4))。本研究提供了 rs2282679 和可能 rs12785878 与中国南方人群 25(OH)D 和维生素 D 不足之间关联的独立证据。

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