FOXO3a Gene Polymorphism Associated with Asthma in Indian Population

S. Barkund, Tejas Shah, Nikhil Ambatkar, M. Gadgil, K. Joshi
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引用次数: 22

Abstract

Asthma is a chronic inflammatory disorder delineated by a heightened immunological response due to environmental or genetic factors. Single nucleotide polymorphism studies have shown that FOXO3a plays a pivotal role in maintaining immunoregulation. Polymorphism in FOXO3a has been linked to inflammatory diseases such as chronic obstructive pulmonary disease (COPD), Rheumatoid Arthritis, and Crohn's disease suggesting that FOXO3a may be associated with asthma. Airway inflammation in asthma is characterized by activation of T helper type 2 (Th2) T cells and Foxo family members are reported to play critical roles in the suppression of T cell activation. Thus this study was undertaken to investigate an association between single nucleotide polymorphism of the FOXO3a (rs13217795, C>T transition) gene and asthma in Indian population. To our knowledge we are the first ones reporting an association between FOXO3a and asthma.
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印度人群中FOXO3a基因多态性与哮喘相关
哮喘是一种慢性炎症性疾病,由环境或遗传因素引起的免疫反应增强所描述。单核苷酸多态性研究表明,FOXO3a在维持免疫调节中起着关键作用。FOXO3a多态性与慢性阻塞性肺疾病(COPD)、类风湿性关节炎和克罗恩病等炎症性疾病有关,这表明FOXO3a可能与哮喘有关。哮喘气道炎症的特征是辅助性T型2 (Th2) T细胞的激活,据报道Foxo家族成员在抑制T细胞激活中起关键作用。因此,本研究旨在探讨印度人群中FOXO3a (rs13217795, C>T过渡)基因单核苷酸多态性与哮喘的关系。据我们所知,我们是第一个报道FOXO3a和哮喘之间关联的人。
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