Your browser doesn't support javascript.
loading
Sputum gene expression signature of 6 biomarkers discriminates asthma inflammatory phenotypes.
Baines, Katherine J; Simpson, Jodie L; Wood, Lisa G; Scott, Rodney J; Fibbens, Naomi L; Powell, Heather; Cowan, Douglas C; Taylor, D Robin; Cowan, Jan O; Gibson, Peter G.
Afiliação
  • Baines KJ; Priority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, Australia; Department of Respiratory and Sleep Medicine, John Hunter Hospital, New Lambton Heights, Australia. Electronic address: katherine.baines@newcastle
  • Simpson JL; Priority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, Australia; Department of Respiratory and Sleep Medicine, John Hunter Hospital, New Lambton Heights, Australia.
  • Wood LG; Priority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, Australia; Department of Respiratory and Sleep Medicine, John Hunter Hospital, New Lambton Heights, Australia.
  • Scott RJ; Priority Research Centre of Information Based Medicine, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, Australia.
  • Fibbens NL; Priority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, Australia; Department of Respiratory and Sleep Medicine, John Hunter Hospital, New Lambton Heights, Australia.
  • Powell H; Priority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, Australia; Department of Respiratory and Sleep Medicine, John Hunter Hospital, New Lambton Heights, Australia.
  • Cowan DC; Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
  • Taylor DR; Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
  • Cowan JO; Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
  • Gibson PG; Priority Research Centre for Asthma and Respiratory Diseases, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, Australia; Department of Respiratory and Sleep Medicine, John Hunter Hospital, New Lambton Heights, Australia.
J Allergy Clin Immunol ; 133(4): 997-1007, 2014 Apr.
Article em En | MEDLINE | ID: mdl-24582314
ABSTRACT

BACKGROUND:

Airway inflammation is associated with asthma exacerbation risk, treatment response, and disease mechanisms.

OBJECTIVE:

This study aimed to identify and validate a sputum gene expression signature that discriminates asthma inflammatory phenotypes.

METHODS:

An asthma phenotype biomarker discovery study generated gene expression profiles from induced sputum of 47 asthmatic patients. A clinical validation study (n = 59 asthmatic patients) confirmed differential expression of key genes. A 6-gene signature was identified and evaluated for reproducibility (n = 30 asthmatic patients and n = 20 control subjects) and prediction of inhaled corticosteroid (ICS) response (n = 71 asthmatic patients). Receiver operating characteristic curves were calculated, and area under the curve (AUC) values were reported.

RESULTS:

From 277 differentially expressed genes between asthma inflammatory phenotypes, we identified 23 genes that showed highly significant differential expression in both the discovery and validation populations. A signature of 6 genes, including Charcot-Leydon crystal protein (CLC); carboxypeptidase A3 (CPA3); deoxyribonuclease I-like 3 (DNASE1L3); IL-1ß (IL1B); alkaline phosphatase, tissue-nonspecific isozyme (ALPL); and chemokine (C-X-C motif) receptor 2 (CXCR2), was reproducible and could significantly (P < .0001) discriminate eosinophilic asthma from other phenotypes, including patients with noneosinophilic asthma (AUC, 89.6%), paucigranulocytic asthma (AUC, 92.6%), or neutrophilic asthma (AUC, 91.4%) and healthy control subjects (AUC, 97.6%), as well as discriminating patients with neutrophilic asthma from those with paucigranulocytic asthma (AUC, 85.7%) and healthy control subjects (AUC, 90.8). The 6-gene signature predicted ICS response (>12% change in FEV1; AUC, 91.5%). ICS treatment reduced the expression of CLC, CPA3, and DNASE1L3 in patients with eosinophilic asthma.

CONCLUSIONS:

A sputum gene expression signature of 6 biomarkers reproducibly and significantly discriminates inflammatory phenotypes of asthma and predicts ICS treatment response. This signature has the potential to become a useful diagnostic tool to assist in the clinical diagnosis and management of asthma.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Asma / Escarro / Transcriptoma Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Asma / Escarro / Transcriptoma Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2014 Tipo de documento: Article