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10.1164/rccm.201406-1099OC

http://scihub22266oqcxt.onion/10.1164/rccm.201406-1099OC
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C4294630!4294630!25338189
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suck abstract from ncbi


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pmid25338189      Am+J+Respir+Crit+Care+Med 2014 ; 190 (12): 1363-72
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  • Gene Expression in Relation to Exhaled Nitric Oxide Identifies Novel Asthma Phenotypes with Unique Biomolecular Pathways #MMPMID25338189
  • Modena BD; Tedrow JR; Milosevic J; Bleecker ER; Meyers DA; Wu W; Bar-Joseph Z; Erzurum SC; Gaston BM; Busse WW; Jarjour NN; Kaminski N; Wenzel SE
  • Am J Respir Crit Care Med 2014[Dec]; 190 (12): 1363-72 PMID25338189show ga
  • Rationale: Although asthma is recognized as a heterogeneous disease associated with clinical phenotypes, the molecular basis of these phenotypes remains poorly understood. Although genomic studies have successfully broadened our understanding in diseases such as cancer, they have not been widely used in asthma studies. Objectives: To link gene expression patterns to clinical asthma phenotypes. Methods: We used a microarray platform to analyze bronchial airway epithelial cell gene expression in relation to the asthma biomarker fractional exhaled nitric oxide (FeNO) in 155 subjects with asthma and healthy control subjects from the Severe Asthma Research Program (SARP). Measurements and Main Results: We first identified a diverse set of 549 genes whose expression correlated with FeNO. We used k-means to cluster the patient samples according to the expression of these genes, identifying five asthma clusters/phenotypes with distinct clinical, physiological, cellular, and gene transcription characteristics?termed ?subject clusters? (SCs). To then investigate differences in gene expression between SCs, a total of 1,384 genes were identified that highly differentiated the SCs at an unadjusted P value?
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