Reis Jared P, Michos Erin D, Selvin Elizabeth, Pankow James S, Lutsey Pamela L
From the Division of Cardiovascular Sciences, National Heart, Lung, and Blood Institute, Bethesda, MD (JPR); the Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD (EDM); the Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD (ES); and the Division of Epidemiology and Community Health, University of Minnesota, Minneapolis, MN (JSP and PLL).
Am J Clin Nutr. 2015 Jun;101(6):1232-40. doi: 10.3945/ajcn.115.107334. Epub 2015 Apr 29.
Low 25-hydroxyvitamin D [25(OH)D] is associated with diabetes, but few studies have examined racially diverse populations while also accounting for key vitamin D-binding protein (DBP) gene polymorphisms.
We sought to evaluate whether the association between 25(OH)D and incident diabetes varied by race and important DBP single nucleotide polymorphisms (SNPs).
We studied 10,222 adults (8120 whites, 2102 blacks) aged 46-70 y at baseline (1990-1992) from the ARIC (Atherosclerosis Risk in Communities) Study with follow-up for incident diabetes ascertained during study visits conducted in 1993-1995 and 1996-1998. Adjusted HRs and their 95% CIs for diabetes were estimated according to 25(OH)D status.
During follow-up there were 750 incident cases of diabetes. The association of 25(OH)D with diabetes varied by race (P-interaction = 0.004). Among whites, the adjusted HR for diabetes corresponding to each additional SD higher 25(OH)D concentration (21.3 nmol/L) was 0.95 (95% CI: 0.91, 0.99). No significant association was observed among blacks (HR: 1.06; 95% CI: 0.99, 1.14). There was evidence that the A allele at rs4588 and the T allele at rs7041, which are reported to be associated with high and low DBP concentrations, respectively, modified the association between 25(OH)D and diabetes among whites (P-interaction < 0.05 for both) but not blacks (P-interaction > 0.50 for both).
In this large, community-based study, low 25(OH)D concentrations were associated with diabetes among whites but not blacks. Interactions by key DBP SNPs varied between genotypes associated with either high or low DBP concentrations among whites but not blacks. Nevertheless, the findings from this prospective study suggest that there are important differences in the association of 25(OH)D with incident diabetes between white and black adults.
低水平的25-羟基维生素D[25(OH)D]与糖尿病相关,但很少有研究在考虑关键维生素D结合蛋白(DBP)基因多态性的同时,对不同种族人群进行研究。
我们试图评估25(OH)D与新发糖尿病之间的关联是否因种族和重要的DBP单核苷酸多态性(SNP)而有所不同。
我们对来自社区动脉粥样硬化风险(ARIC)研究的10222名46至70岁的成年人(8120名白人,2102名黑人)进行了研究,这些人在基线时(1990 - 1992年)入组,随访新发糖尿病情况,随访期间的研究访视在1993 - 1995年和1996 - 1998年进行。根据25(OH)D状态估计糖尿病的校正风险比(HR)及其95%置信区间(CI)。
随访期间有750例新发糖尿病病例。25(OH)D与糖尿病的关联因种族而异(P交互作用 = 0.004)。在白人中,25(OH)D浓度每增加一个标准差(21.3 nmol/L)对应的糖尿病校正HR为0.95(95%CI:0.91,0.99)。在黑人中未观察到显著关联(HR:1.06;95%CI:0.99,1.14)。有证据表明,rs4588处的A等位基因和rs7041处的T等位基因分别与高和低DBP浓度相关,它们改变了白人中25(OH)D与糖尿病之间的关联(两者的P交互作用均<0.05),但黑人中未改变(两者的P交互作用均>0.50)。
在这项基于社区的大型研究中,低25(OH)D浓度与白人中的糖尿病相关,但与黑人无关。关键DBP SNP的相互作用在白人中与高或低DBP浓度相关的基因型之间有所不同,但在黑人中并非如此。尽管如此,这项前瞻性研究的结果表明,白人和黑人成年人中25(OH)D与新发糖尿病之间的关联存在重要差异。