Ruse Charlotte E, Hill Maureen C, Burton Paul R, Connolly Martin J, Wardlaw Andrew J, Parker Stuart G
Institute for Lung Health, University of Leicester, Leicester, United Kingdom.
J Am Geriatr Soc. 2003 Sep;51(9):1265-9. doi: 10.1046/j.1532-5415.2003.51411.x.
To test the hypothesis that genetic polymorphisms in the beta subunit of the high-affinity immunoglobulin E (IgE) receptor are associated with late-onset airflow obstruction.
Case-control candidate gene association study.
Department of Medicine for the Elderly and Respiratory Medicine in three teaching hospitals in Leicester and Manchester, United Kingdom.
Cases with late-onset airflow obstruction with age-, sex-, and geographically matched controls.
Subjects were genotyped for two polymorphisms of the beta subunit of the high-affinity IgE receptor (RsaI intron 2 and RsaI exon 7). The association between the polymorphisms and phenotypes was examined using contingency tables and linear regression models.
Two hundred eighty-three cases and 144 controls were genotyped. RsaI exon 7 AA was associated with eczema (odds ratio (OR)=2.27, 95% confidence interval (CI)=1.17-4.38, P=.015). No other associations were found. Total serum IgE levels were significantly higher in cases than controls (adjusted OR for high/low IgE=2.56, 95% CI=1.53-4.28, P<.001).
Serum IgE levels, but not the high-affinity IgE receptor polymorphisms, were associated with late-onset airflow obstruction, suggesting that interaction between environmental and genetic factors controlling serum IgE levels and disease pathogenesis may differ between early- and late-onset airflow obstruction phenotypes.
检验高亲和力免疫球蛋白E(IgE)受体β亚基的基因多态性与迟发性气流受限相关的假设。
病例对照候选基因关联研究。
英国莱斯特和曼彻斯特的三家教学医院的老年医学科和呼吸内科。
迟发性气流受限患者以及年龄、性别和地理位置匹配的对照。
对受试者的高亲和力IgE受体β亚基的两种多态性(RsaI内含子2和RsaI外显子7)进行基因分型。使用列联表和线性回归模型检查多态性与表型之间的关联。
对283例病例和144例对照进行了基因分型。RsaI外显子7 AA与湿疹相关(比值比(OR)=2.27,95%置信区间(CI)=1.17 - 4.38,P = 0.015)。未发现其他关联。病例组的总血清IgE水平显著高于对照组(高/低IgE的调整OR = 2.56,95% CI = 1.53 - 4.28,P < 0.001)。
血清IgE水平而非高亲和力IgE受体多态性与迟发性气流受限相关,这表明控制血清IgE水平的环境和遗传因素之间的相互作用以及疾病发病机制在早发性和迟发性气流受限表型之间可能有所不同。