Personalised Medicine and Asthma Diagnostics/Management

被引:21
作者
Wadsworth, Samuel J. [1 ,2 ]
Sandford, Andrew J. [1 ,2 ]
机构
[1] St Pauls Hosp, Inst Heart & Lung Hlth, UBC James Hogg Res Ctr, Vancouver, BC V6Z 1Y6, Canada
[2] Univ British Columbia, Dept Med, Vancouver, BC, Canada
关键词
Asthma; Personalised medicine; Pharmacogenetics; Pharmacogenomics; Biomarkers; Personalised drug testing; Tissue engineering; Diagnostics; Management; EXHALED NITRIC-OXIDE; HUMAN BETA(2)-ADRENERGIC RECEPTOR; GENOME-WIDE ASSOCIATION; ACTIVATION-REGULATED CHEMOKINE; IMPROVED LUNG-FUNCTION; AIRWAY SMOOTH-MUSCLE; BREATH TEMPERATURE; GLUCOCORTICOID-RECEPTOR; GENETIC POLYMORPHISMS; STEROID RESISTANCE;
D O I
10.1007/s11882-012-0325-9
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Human beings come in all shapes and sizes. Heterogeneity makes life interesting, but leads to inter-individual variation in disease susceptibility and response to therapy. One major health challenge is to develop "personalised medicine"; therapeutic interventions tailored to an individual to ensure optimal treatment of disease. Asthma is a heterogeneous disease with several different phenotypes triggered by multiple gene-environment interactions. Inhaled corticosteroids and beta 2-agonists have been the mainstay asthma therapies for 30 years, but they are not effective in all patients, while high costs and side-effects also drive the need for better targeted treatment of asthma. Pharmacogenetics is the study of variations in the genetic code for proteins in signaling pathways targeted by pharmacological therapies. Biomarkers are biological markers obtained from patients that can aid in asthma diagnosis, prediction of treatment response, and monitoring of disease control. This review presents a broad discussion of the use of genetic profiling and biomarkers to better diagnose, monitor, and tailor the treatment of asthmatics. We also discuss possible future developments in personalised medicine, including the construction of artificially engineered airway tissues containing a patient's own cells for use as personalised drug-testing tools.
引用
收藏
页码:118 / 129
页数:12
相关论文
共 131 条
[21]   Anti-IL-5 treatment reduces deposition of ECM proteins in the bronchial subepithelial basement membrane of mild atopic asthmatics [J].
Flood-Page, P ;
Menzies-Gow, A ;
Phipps, S ;
Ying, S ;
Wangoo, A ;
Ludwig, MS ;
Barnes, N ;
Robinson, D ;
Kay, AB .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (07) :1029-1036
[22]  
García-Caballero T, 2006, HISTOL HISTOPATHOL, V21, P227, DOI 10.14670/HH-21.227
[23]   Effects of Interleukin-13 Blockade on Allergen-induced Airway Responses in Mild Atopic Asthma [J].
Gauvreau, Gail M. ;
Boulet, Louis-Philippe ;
Cockcroft, Donald W. ;
FitzGerald, J. Mark ;
Carlsten, Chris ;
Davis, Beth E. ;
Deschesnes, Francine ;
Duong, MyLinh ;
Durn, Billie L. ;
Howie, Karen J. ;
Hui, Linda ;
Kasaian, Marion T. ;
Killian, Kieran J. ;
Strinich, Tara X. ;
Watson, Richard M. ;
Nathalie, Y. ;
Zhou, Simon ;
Raible, Donald ;
O'Byrne, Paul M. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2011, 183 (08) :1007-1014
[24]   Angiogenic markers in breath condensate identify non-small cell lung cancer [J].
Gessner, C. ;
Rechner, B. ;
Hammerschmidt, S. ;
Kuhn, H. ;
Hoheisel, G. ;
Sack, U. ;
Ruschpler, P. ;
Wirtz, H. .
LUNG CANCER, 2010, 68 (02) :177-184
[25]  
Goldstein J., 1998, CLIN REVIEW1998
[26]   Analysis of induced sputum in adults with asthma: identification of subgroup with isolated sputum neutrophilia and poor response to inhaled corticosteroids [J].
Green, RH ;
Brightling, CE ;
Woltmann, G ;
Parker, D ;
Wardlaw, AJ ;
Pavord, ID .
THORAX, 2002, 57 (10) :875-879
[27]   AMINO-TERMINAL POLYMORPHISMS OF THE HUMAN BETA(2)-ADRENERGIC RECEPTOR IMPART DISTINCT AGONIST-PROMOTED REGULATORY PROPERTIES [J].
GREEN, SA ;
TURKI, J ;
INNIS, M ;
LIGGETT, SB .
BIOCHEMISTRY, 1994, 33 (32) :9414-9419
[28]  
GREEN SA, 1993, J BIOL CHEM, V268, P23116
[29]   INFLUENCE OF BETA(2)-ADRENERGIC RECEPTOR GENOTYPES ON SIGNAL-TRANSDUCTION IN HUMAN AIRWAY SMOOTH-MUSCLE CELLS [J].
GREEN, SA ;
TURKI, J ;
BEJARANO, P ;
HALL, IP ;
LIGGETT, SB .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 13 (01) :25-33
[30]   Volume transport across tracheal and bronchial airway epithelia in a tubular culture system [J].
Grubb, BR ;
Schiretz, FR ;
Boucher, RC .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 273 (01) :C21-C29