Laprise Catherine, Sladek Robert, Ponton André, Bernier Marie-Claude, Hudson Thomas J, Laviolette Michel
Université du Québec à Chicoutimi, Department of Fundamental Sciences, Chicoutimi, Canada.
BMC Genomics. 2004 Mar 23;5(1):21. doi: 10.1186/1471-2164-5-21.
Asthma pathogenesis and susceptibility involves a complex interplay between genetic and environmental factors. Their interaction modulates the airway inflammation and remodelling processes that are present even in mild asthma and governs the appearance and severity of symptoms of airway hyperresponsiveness. While asthma is felt to develop as the result of interaction among many different genes and signalling pathways, only a few genes have been linked to an increased risk of developing this condition.
We report the results of expression microarray studies using tissue obtained from bronchial biopsies of healthy controls and of subjects with allergic asthma, both before and following inhaled corticotherapy. We identified 79 genes that show significant differences in expression (following Bonferroni cutoff using p < 6.6 x 10(-6) to correct for multiple testing) in asthmatics compared to controls at significance levels. These included 21 genes previously implicated in asthma, such as NOS2A and GPX3, as well as new potential candidates, such as ALOX15, CTSC and CX3CR1. The expression levels of one third of these transcripts were partially or completely corrected following inhaled corticosteroid therapy.
The study shows that bronchial biopsies obtained from healthy and asthmatic subjects display distinct expression profiles. These differences provide a global view of physiopathologic processes active in the asthmatic lung and may provide invaluable help to clarify the natural history of asthma.
哮喘的发病机制和易感性涉及遗传和环境因素之间复杂的相互作用。它们的相互作用调节气道炎症和重塑过程,这些过程即使在轻度哮喘中也存在,并决定气道高反应性症状的出现和严重程度。虽然哮喘被认为是由许多不同基因和信号通路之间的相互作用导致的,但只有少数基因与患此病的风险增加有关。
我们报告了使用从健康对照者以及过敏性哮喘患者的支气管活检组织中获取的样本进行表达微阵列研究的结果,这些样本分别在吸入皮质激素治疗之前和之后获取。我们鉴定出79个基因,与对照组相比,这些基因在哮喘患者中的表达显示出显著差异(在使用p < 6.6 x 10(-6)进行Bonferroni校正以校正多重检验后,具有显著性水平)。其中包括21个先前与哮喘相关的基因,如NOS2A和GPX3,以及新的潜在候选基因,如ALOX15、CTSC和CX3CR1。吸入皮质类固醇治疗后,这些转录本中有三分之一的表达水平部分或完全得到纠正。
该研究表明,从健康受试者和哮喘患者获取的支气管活检组织显示出不同的表达谱。这些差异提供了哮喘肺中活跃的生理病理过程的整体视图,并可能为阐明哮喘的自然史提供宝贵的帮助。