Grant: CIHR Fellowship
University of British Columbia
$90,000.00
Characterization of novel biomarkers of exacerbations of chronic obstructive pulmonary disease (COPD)
FY 2014-15
Summary
Chronic obstructive pulmonary disease (COPD) is characterized by progressive loss of lung function causing shortness of breath, cough and sputum production. It affects 1.7 million Canadians, and is responsible for 11,000 deaths, and over 70,000 hospital admissions annually in Canada. Most of its burden is due to "lung attacks". These acute exacerbations of COPD (AECOPD) are often triggered by respiratory infections. AECOPD management has not changed much in the last 30 years, and available therapies remain modestly effective. Moreover, unlike heart attacks, there are no simple blood biomarkers (measureable indicator of a biological state) available for AECOPD. As a result, AECOPD is generally a diagnosis of exclusion, and misdiagnosis and severe diagnosis delays are common, leading to poor outcomes for patients. A simple reliable blood test for AECOPD would be a game-changer and enable clinicians to promptly and accurately identify these early in their course when treatments are most effective. This study will assess whether there are novel blood biomarkers that are diagnostic of AECOPD that could be used in the clinical setting. We will be evaluating biomarkers in blood samples collected at several time points in 250 COPD patients who were hospitalized with AECOPD between 2012-2014. These will be compared to 75 "control" samples collected from COPD patients who were not hospitalized and considered to be clinically stable at blood draw, and then replicated in 150 COPD patients who were likewise hospitalized with AECOPD at a different hospital. The amount of different biomarkers and how they change over time after AECOPD will be measured using commercially available kits and more complex arrays that can detect differences in gene expression. This study will investigate novel biological pathways that are most plausible biomarker candidates with the aim of developing an assay that can easily be used clinically, ultimately facilitating the diagnosis of AECOPD.
Department
Program
CIHR Fellowship
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
318853
Name
Labonté Laura E
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Clinical
Prcname2
Fellowships - Post-PhD
Projecttitle
Characterization of novel biomarkers of exacerbations of chronic obstructive pulmonary disease (COPD)
Programtype2
Fellowship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$90,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Biomarkers; Copd; Diagnositc; Exacerbations; Translational
Abstract
Chronic obstructive pulmonary disease (COPD) is characterized by progressive loss of lung function causing shortness of breath, cough and sputum production. It affects 1.7 million Canadians, and is responsible for 11,000 deaths, and over 70,000 hospital admissions annually in Canada. Most of its burden is due to "lung attacks". These acute exacerbations of COPD (AECOPD) are often triggered by respiratory infections. AECOPD management has not changed much in the last 30 years, and available therapies remain modestly effective. Moreover, unlike heart attacks, there are no simple blood biomarkers (measureable indicator of a biological state) available for AECOPD. As a result, AECOPD is generally a diagnosis of exclusion, and misdiagnosis and severe diagnosis delays are common, leading to poor outcomes for patients. A simple reliable blood test for AECOPD would be a game-changer and enable clinicians to promptly and accurately identify these early in their course when treatments are most effective. This study will assess whether there are novel blood biomarkers that are diagnostic of AECOPD that could be used in the clinical setting. We will be evaluating biomarkers in blood samples collected at several time points in 250 COPD patients who were hospitalized with AECOPD between 2012-2014. These will be compared to 75 "control" samples collected from COPD patients who were not hospitalized and considered to be clinically stable at blood draw, and then replicated in 150 COPD patients who were likewise hospitalized with AECOPD at a different hospital. The amount of different biomarkers and how they change over time after AECOPD will be measured using commercially available kits and more complex arrays that can detect differences in gene expression. This study will investigate novel biological pathways that are most plausible biomarker candidates with the aim of developing an assay that can easily be used clinically, ultimately facilitating the diagnosis of AECOPD.
Competitiondate
201411
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Labonté, Laura E
Approvedterm
2 ans 0 mois
Cihrcontribution2
~ $90,000~ $0~