Yan Xiting, Chu Jen-Hwa, Gomez Jose, Koenigs Maria, Holm Carole, He Xiaoxuan, Perez Mario F, Zhao Hongyu, Mane Shrikant, Martinez Fernando D, Ober Carole, Nicolae Dan L, Barnes Kathleen C, London Stephanie J, Gilliland Frank, Weiss Scott T, Raby Benjamin A, Cohn Lauren, Chupp Geoffrey L
1 Section of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine.
Am J Respir Crit Care Med. 2015 May 15;191(10):1116-25. doi: 10.1164/rccm.201408-1440OC.
The airway transcriptome includes genes that contribute to the pathophysiologic heterogeneity seen in individuals with asthma.
We analyzed sputum gene expression for transcriptomic endotypes of asthma (TEA), gene signatures that discriminate phenotypes of disease.
Gene expression in the sputum and blood of patients with asthma was measured using Affymetrix microarrays. Unsupervised clustering analysis based on pathways from the Kyoto Encyclopedia of Genes and Genomes was used to identify TEA clusters. Logistic regression analysis of matched blood samples defined an expression profile in the circulation to determine the TEA cluster assignment in a cohort of children with asthma to replicate clinical phenotypes.
Three TEA clusters were identified. TEA cluster 1 had the most subjects with a history of intubation (P = 0.05), a lower prebronchodilator FEV1 (P = 0.006), a higher bronchodilator response (P = 0.03), and higher exhaled nitric oxide levels (P = 0.04) compared with the other TEA clusters. TEA cluster 2, the smallest cluster, had the most subjects that were hospitalized for asthma (P = 0.04). TEA cluster 3, the largest cluster, had normal lung function, low exhaled nitric oxide levels, and lower inhaled steroid requirements. Evaluation of TEA clusters in children confirmed that TEA clusters 1 and 2 are associated with a history of intubation (P = 5.58 × 10(-6)) and hospitalization (P = 0.01), respectively.
There are common patterns of gene expression in the sputum and blood of children and adults that are associated with near-fatal, severe, and milder asthma.
气道转录组包含一些基因,这些基因导致了哮喘患者中出现的病理生理异质性。
我们分析了痰液基因表达,以寻找哮喘的转录组内型(TEA),即区分疾病表型的基因特征。
使用Affymetrix微阵列测量哮喘患者痰液和血液中的基因表达。基于京都基因与基因组百科全书(KEGG)通路的无监督聚类分析用于识别TEA簇。对匹配的血液样本进行逻辑回归分析,确定循环中的表达谱,以确定一组哮喘儿童的TEA簇分配情况,从而复制临床表型。
识别出三个TEA簇。与其他TEA簇相比,TEA簇1中插管史的受试者最多(P = 0.05),支气管扩张剂使用前的第一秒用力呼气容积(FEV1)较低(P = 0.006),支气管扩张剂反应较高(P = 0.03),呼出一氧化氮水平较高(P = 0.04)。TEA簇2是最小的簇,因哮喘住院的受试者最多(P = 0.04)。TEA簇3是最大的簇,肺功能正常,呼出一氧化氮水平低,吸入类固醇需求较低。对儿童TEA簇的评估证实,TEA簇1和2分别与插管史(P = 5.58×10⁻⁶)和住院史(P = 0.01)相关。
儿童和成人痰液及血液中存在与近乎致命性、重度和轻度哮喘相关的共同基因表达模式。