A Severe Asthma Disease Signature from Gene Expression Profiling of Peripheral Blood from U-BIOPRED Cohorts

被引:135
作者
Bigler, Jeannette [1 ,14 ]
Boedigheimer, Michael [2 ]
Schofield, James P. R. [3 ]
Skipp, Paul J. [3 ]
Corfield, Julie [4 ,5 ]
Rowe, Anthony [6 ]
Sousa, Ana R. [7 ]
Timour, Martin [1 ]
Twehues, Lori [2 ]
Hu, Xuguang [8 ]
Roberts, Graham [9 ]
Welcher, Andrew A. [2 ]
Yu, Wen [1 ,15 ]
Lefaudeux, Diane [10 ]
De Meulder, Bertrand [10 ]
Auffray, Charles [10 ]
Chung, Kian F. [11 ,12 ]
Adcock, Ian M. [11 ,12 ]
Sterk, Peter J. [13 ]
Djukanovic, Ratko [9 ]
机构
[1] Amgen Inc, Seattle, WA USA
[2] Amgen Inc, Thousand Oaks, CA 91320 USA
[3] Southampton Univ, Ctr Biol Sci, Southampton, Hants, England
[4] AstraZeneca R&D, Molndal, Sweden
[5] Areteva R&D, Nottingham, England
[6] Janssen Res & Dev, High Wycombe, Bucks, England
[7] GSK, Resp Therapeut Unit, Stockley Pk, Uxbridge, Middx, England
[8] Amgen Inc, San Francisco, CA USA
[9] Univ Hosp Southampton, Resp Biomed Res Unit, Fac Med, Southampton, Hants, England
[10] Ctr Natl Rech Sci, European Inst Syst Biol & Med, Lyon, France
[11] Imperial Coll, Natl Heart & Lung Inst, London, England
[12] Royal Brompton & Harefield NHS Trust, Biomed Res Unit, London, England
[13] Univ Amsterdam, Acad Med Ctr, Dept Resp Med, Amsterdam, Netherlands
[14] BJ Grp LLC, 3200 NE 92nd St, Seattle, WA 98115 USA
[15] MedImmune LLC, Res Informat, Gaithersburg, MD USA
关键词
biomarker; immune cell; microarray; EOSINOPHILIC ASTHMA; TRANSGLUTAMINASE; 2; PHENOTYPES; MECHANISMS; MICROARRAY; DISCOVERY; HEALTH; CELLS; DIFFERENTIATION; DEXAMETHASONE;
D O I
10.1164/rccm.201604-0866OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Stratification of asthma at the molecular level, especially using accessible biospecimens, could greatly enable patient selection for targeted therapy. Objectives: To determine the value of blood analysis to identify transcriptional differences between clinically defined asthma and nonasthma groups, identify potential patient subgroups based on gene expression, and explore biological pathways associated with identified differences. Methods: Transcriptomic profiles were generated by microarray analysis of blood from 610 patients with asthma and control participants in the U-BIOPRED (Unbiased Biomarkers in Prediction of Respiratory Disease Outcomes) study. Differentially expressed genes (DEGs) were identified by analysis of variance, including covariates for RNA quality, sex, and clinical site, and Ingenuity Pathway Analysis was applied. Patient subgroups based on DEGs were created by hierarchical clustering and topological data analysis. Measurements and Main Results: A total of 1,693 genes were differentially expressed between patients with severe asthma and participants without asthma. The differences from participants without asthma in the nonsmoking severe asthma and mild/moderate asthma subgroups were significantly related (r = 0.76), with a larger effect size in the severe asthma group. The majority of, but not all, differences were explained by differences in circulating immune cell populations. Pathway analysis showed an increase in chemotaxis, migration, and myeloid cell trafficking in patients with severe asthma, decreased B-lymphocyte development and hematopoietic progenitor cells, and lymphoid organ hypoplasia. Cluster analysis of DEGs led to the creation of subgroups among the patients with severe asthma who differed in molecular responses to oral corticosteroids. Conclusions: Blood gene expression differences between clinically defined subgroups of patients with asthma and individuals without asthma, as well as subgroups of patients with severe asthma defined by transcript profiles, show the value of blood analysis in stratifying patients with asthma and identifying molecular pathways for further study.
引用
收藏
页码:1311 / 1320
页数:10
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