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Grant: Environments, Genes and Chronic Disease - LOI

University of British Columbia

$0.00

Genomics, Asthma and Airborne Exposures: From Vulnerability to Prevention

FY 2014-15

Summary
Over past decades, the adverse effects of air pollution on human health have been investigated through independent efforts of epidemiology, toxicology and controlled human exposure models. Recently, genetic information has increased our understanding. However, there is so much genetic data, and it is so complex, that it is difficult to understand how best to use it to help people in the 'real world', especially when genetics and the environment interact with each other (making things even more complicated). We are bringing together a unique team of 10 individual researchers with varied backgrounds to try and harness the full potential of this information and leverage our findings to develop strategies to improve health. Our research skills intersect uniquely upon the following assertion: understanding the relationship between genetic variability, airborne exposures, and epigenetic changes will offer and opportunity for risk modification by distinct interventions. We propose a set of studies to characterize how genes and exposure to inhalants such as air pollution and allergens interact to affect asthma. We think that this can lead to reduced harm but we lack clear evidence and plausibility that the path from genome-level data to reducing the toxicity of harmful inhalants can be realized. Our plan is to use complementary human and animal exposure models to test the effectiveness of agents that modify the relationship between gene and exposure, to provide a rich set of epigenetic data from blood and lung tissue. Then we will use computer models to illuminate discoveries not previously possible. Finally, we will ask how and when this knowledge is desirable to end-users so that it can be transferred in a meaningful way. We focus on air pollution and asthma given our clinical expertise and the worldwide prevalence of this condition, but will aim to construct a model that extends to other exposures and chronic disease conditions.
Program
Environments, Genes and Chronic Disease - LOI
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
324158
Name
Carlsten Christopher
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Environments, Genes and Chronic Disease - LOI
Projecttitle
Genomics, Asthma and Airborne Exposures: From Vulnerability to Prevention
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$0
Cihrequipment2
$0
Programname2
Environments, Genes and Chronic Disease - LOI
Keyworddelim
Air Pollution; Antioxidant; Asthma; Epigenetics; Genetic Variability; Inhaled Steroid; Knowledge Translation; Omics; Vulnerability
Abstract
Over past decades, the adverse effects of air pollution on human health have been investigated through independent efforts of epidemiology, toxicology and controlled human exposure models. Recently, genetic information has increased our understanding. However, there is so much genetic data, and it is so complex, that it is difficult to understand how best to use it to help people in the 'real world', especially when genetics and the environment interact with each other (making things even more complicated). We are bringing together a unique team of 10 individual researchers with varied backgrounds to try and harness the full potential of this information and leverage our findings to develop strategies to improve health. Our research skills intersect uniquely upon the following assertion: understanding the relationship between genetic variability, airborne exposures, and epigenetic changes will offer and opportunity for risk modification by distinct interventions. We propose a set of studies to characterize how genes and exposure to inhalants such as air pollution and allergens interact to affect asthma. We think that this can lead to reduced harm but we lack clear evidence and plausibility that the path from genome-level data to reducing the toxicity of harmful inhalants can be realized. Our plan is to use complementary human and animal exposure models to test the effectiveness of agents that modify the relationship between gene and exposure, to provide a rich set of epigenetic data from blood and lung tissue. Then we will use computer models to illuminate discoveries not previously possible. Finally, we will ask how and when this knowledge is desirable to end-users so that it can be transferred in a meaningful way. We focus on air pollution and asthma given our clinical expertise and the worldwide prevalence of this condition, but will aim to construct a model that extends to other exposures and chronic disease conditions.
Competitiondate
201501
Approvedterm2
0 yr 6 mths
Pinamesdelim
Carlsten, Christopher; Brinkman, Fiona S
Approvedterm
0 an 6 mois
University of British Columbia - $0 Grant (2014-15) | Canada Spends