Channing Laboratory, Brigham and Women's Hospital, Boston, Mass 02115, USA.
J Allergy Clin Immunol. 2012 Feb;129(2):368-73, 373.e1-5. doi: 10.1016/j.jaci.2011.09.034. Epub 2011 Nov 1.
It has recently been shown that vitamin D deficiency can increase asthma development and severity and that variations in vitamin D receptor genes are associated with asthma susceptibility.
We sought to find genetic factors that might interact with vitamin D levels to affect the risk of asthma exacerbation.
We conducted a genome-wide study of gene-vitamin D interaction on asthma exacerbations using population-based and family-based approaches on 403 subjects and trios from the Childhood Asthma Management Program. Twenty-three polymorphisms with significant interactions were studied in a replication analysis in 584 children from a Costa Rican cohort.
We identified 3 common variants in the class I MHC-restricted T cell-associated molecule gene (CRTAM) that were associated with an increased rate of asthma exacerbations based on the presence of a low circulating vitamin D level. These results were replicated in a second independent population (unadjusted combined interaction, P = .00028-.00097; combined odds ratio, 3.28-5.38). One variant, rs2272094, is a nonsynonymous coding polymorphism of CRTAM. Functional studies on cell lines confirmed the interaction of vitamin D and rs2272094 on CRTAM expression. CRTAM is highly expressed in activated human CD8(+) and natural killer T cells, both of which have been implicated in asthmatic patients.
The findings highlight an important gene-environment interaction that elucidates the role of vitamin D and CD8(+) and natural killer T cells in asthma exacerbation in a genome-wide gene-environment interaction study that has been replicated in an independent population. The results suggest the potential importance of maintaining adequate vitamin D levels in subsets of high-risk asthmatic patients.
最近的研究表明,维生素 D 缺乏会增加哮喘的发生和严重程度,维生素 D 受体基因的变异与哮喘易感性有关。
我们试图寻找可能与维生素 D 水平相互作用影响哮喘加重风险的遗传因素。
我们使用基于人群和基于家庭的方法,对来自儿童哮喘管理计划的 403 名受试者和 3 对家族进行了全基因组维生素 D 与基因相互作用的研究。在哥斯达黎加队列的 584 名儿童中进行了一项复制分析,研究了 23 个具有显著相互作用的多态性。
我们在 Class I MHC 限制性 T 细胞相关分子基因(CRTAM)中发现了 3 个常见的变异体,这些变异体与低循环维生素 D 水平存在时哮喘加重的发生率增加有关。这些结果在第二个独立的人群中得到了复制(未经调整的综合相互作用,P =.00028-.00097;综合优势比,3.28-5.38)。一个变体,rs2272094,是 CRTAM 的非同义编码多态性。细胞系的功能研究证实了维生素 D 和 rs2272094 对 CRTAM 表达的相互作用。CRTAM 在激活的人 CD8(+)和自然杀伤 T 细胞中高度表达,这两种细胞都与哮喘患者有关。
这些发现突出了一个重要的基因-环境相互作用,该相互作用通过全基因组基因-环境相互作用研究阐明了维生素 D 与 CD8(+)和自然杀伤 T 细胞在哮喘加重中的作用,该研究在独立人群中得到了复制。结果表明,在高危哮喘患者亚群中维持足够的维生素 D 水平具有潜在的重要性。