Translating Asthma: Dissecting the Role of Metabolomics, Genomics and Personalized Medicine

被引:8
作者
Bush, Andrew [1 ,2 ,3 ]
机构
[1] Imperial Coll, Dept Pediat, London, England
[2] Natl Heart & Lung Inst, Dept Pediat Respirol, London, England
[3] Royal Brompton Harefield NHS Fdn Trust, Dept Pediat Resp Med, London, England
关键词
Biomarker; Transcriptomics; Bronchial biopsy; Bronchial brushings; Induced sputum; Airway inflammation; Asthma phenotype; Endotype; VOLATILE ORGANIC-COMPOUNDS; GENE-EXPRESSION; LUNG-FUNCTION; CHILDHOOD ASTHMA; CLUSTER-ANALYSIS; NATIONAL HEART; CHILDREN; INFLAMMATION; BLOOD; PHENOTYPES;
D O I
10.1007/s12098-017-2520-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The management of asthma has largely stagnated over the last 25 years, but we are at the dawning of a new age wherein -omics technology can help us manage the disease objectively and rationally. Even in this new scientific age, getting the basics of asthma management right remains essential. The new technologies which can be applied to multiple biological samples include genomics (study of the genome), transcriptomics (gene transcription), lipidomics, proteomics and metabolomics (lipids, proteins and metabolites, respectively) and breathomics, using exhaled breath as a source of biomarkers, which is of particular interest in view of its non-invasive nature in pediatrics. Important applications will include the diagnosis of airways disease, including its components; the pathways driving airway pathology; monitoring the response to treatment; and measuring future risk (asthma attacks, poor lung growth trajectory). With the advent of a wide range of novel biologicals to treat asthma, -omics technology to personalize therapy will be especially important. The U-BIOPRED (Europe) and SARP (USA) groups have been most active in this field, especially using bronchoscopically obtained samples to perform cluster analyses to define new asthma endotypes. However, stability over time and consistency between investigators is imperfect. This is perhaps unsurprising; results of biomarker studies in asthma will be a composite of the underlying disease, the (variable) effects of adverse drivers such as allergen exposure and pollution, the effects of treatment, and the effects of adherence or otherwise to treatment. Ultimately, the aim should be an exhaled breath based tool with a rapid result that can be used as a routine in the clinic. However, at the moment, there are as yet no clinical applications in children of -omics technology.
引用
收藏
页码:643 / 650
页数:8
相关论文
共 55 条
[1]   The ENFUMOSA cross-sectional European multicentre study of the clinical phenotype of chronic severe asthma [J].
Abraham, B ;
Antó, JM ;
Barreiro, E ;
Bel, EHD ;
Bonsignore, G ;
Bousquet, J ;
Castellsague, J ;
Chanez, P ;
Cibella, F ;
Cuttitta, G ;
Dahlén, B ;
Dahlén, SE ;
Drews, N ;
Djukanovic, R ;
Fabbri, LM ;
Folkerts, G ;
Gaga, M ;
Gratziou, C ;
Guerrera, G ;
Holgate, ST ;
Howarth, PH ;
Johnston, SL ;
Kanniess, F ;
Kips, JC ;
Kerstjens, HAM ;
Kumlin, M ;
Magnussen, H ;
Nijkamp, FP ;
Papageorgiou, N ;
Papi, A ;
Postma, DS ;
Pauwels, RA ;
Rabe, KF ;
Richter, K ;
Roldaan, AC ;
Romagnoli, M ;
Roquet, A ;
Sanjuas, C ;
Siafakas, NM ;
Timens, W ;
Tzanakis, N ;
Vachier, I ;
Vignola, AM ;
Watson, L ;
Yourgioti, G .
EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (03) :470-477
[2]   Worsening of asthma in children allergic to cats, after indirect exposure to cat at school [J].
Almqvist, C ;
Wickman, M ;
Perfetti, L ;
Berglind, N ;
Renström, A ;
Hedrén, M ;
Larsson, K ;
Hedlin, G ;
Malmberg, P .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 163 (03) :694-698
[3]   A Deep Dive into Asthma Transcriptomics Lessons from U-BIOPRED [J].
Altman, Matthew C. ;
Busse, William W. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2017, 195 (10) :1279-1280
[4]   COMMUNITY OUTBREAKS OF ASTHMA ASSOCIATED WITH INHALATION OF SOYBEAN DUST [J].
ANTO, JM ;
SUNYER, J ;
RODRIGUEZROISIN, R ;
SUAREZCERVERA, M ;
VAZQUEZ, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (17) :1097-1102
[5]   An Integrative Systems Biology Approach to Understanding Pulmonary Diseases [J].
Auffray, Charles ;
Adcock, Ian M. ;
Chung, Kian Fan ;
Djukanovic, Ratko ;
Pison, Christophe ;
Sterk, Peter J. .
CHEST, 2010, 137 (06) :1410-1416
[6]   Trajectories of Lung Function during Childhood [J].
Belgrave, Danielle C. M. ;
Buchan, Lain ;
Bishop, Christopher ;
Lowe, Lesley ;
Simpson, Angela ;
Custovic, Adnan .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2014, 189 (09) :1101-1109
[7]   A Distinct Low Lung Function Trajectory from Childhood to the Fourth Decade of Life [J].
Berry, Cristine E. ;
Billheimer, Dean ;
Jenkins, Isaac C. ;
Lu, Zhenqiang J. ;
Stern, Debra A. ;
Gerald, Lynn B. ;
Carr, Tara F. ;
Guerra, Stefano ;
Morgan, Wayne J. ;
Wright, Anne L. ;
Martinez, Fernando D. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2016, 194 (05) :607-612
[8]   A Severe Asthma Disease Signature from Gene Expression Profiling of Peripheral Blood from U-BIOPRED Cohorts [J].
Bigler, Jeannette ;
Boedigheimer, Michael ;
Schofield, James P. R. ;
Skipp, Paul J. ;
Corfield, Julie ;
Rowe, Anthony ;
Sousa, Ana R. ;
Timour, Martin ;
Twehues, Lori ;
Hu, Xuguang ;
Roberts, Graham ;
Welcher, Andrew A. ;
Yu, Wen ;
Lefaudeux, Diane ;
De Meulder, Bertrand ;
Auffray, Charles ;
Chung, Kian F. ;
Adcock, Ian M. ;
Sterk, Peter J. ;
Djukanovic, Ratko .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2017, 195 (10) :1311-1320
[9]   Corticosteroid responsiveness and clinical characteristics in childhood difficult asthma [J].
Bossley, C. J. ;
Saglani, S. ;
Kavanagh, C. ;
Payne, D. N. R. ;
Wilson, N. ;
Tsartsali, L. ;
Rosenthal, M. ;
Balfour-Lynn, I. M. ;
Nicholson, A. G. ;
Bush, A. .
EUROPEAN RESPIRATORY JOURNAL, 2009, 34 (05) :1052-1059
[10]   Pediatric severe asthma is characterized by eosinophilia and remodeling without TH2 cytokines [J].
Bossley, Cara J. ;
Fleming, Louise ;
Gupta, Atul ;
Regamey, Nicolas ;
Frith, Jennifer ;
Oates, Timothy ;
Tsartsali, Lemonia ;
Lloyd, Clare M. ;
Bush, Andrew ;
Saglani, Sejal .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2012, 129 (04) :974-U469