Grant: Project Grant - Priority Announcement: IMHA: Oral Health
University of British Columbia
$100,000.00
Acute human gingivitis systems biology
EF 2022-23
Résumé
.
Significance-Inflammation is the body's protective response to infection. Inflammation normally turns off to allow healing. Prolonged inflammation results in diseases, e.g., gingivitis, periodontitis, arthritis and fibrosis. Gingivitis (mild gum inflammation) can progress to severe periodontitis to ultimately cause jaw bone and tooth loss. Periodontal disease is common-in the US, 47% of adults >30 years have gum disease, rising to 70% at >65 years-and is associated with an increased risk of other serious conditions, e.g. diabetes, heart attack and rheumatoid arthritis. Thus, preventing periodontitis reduces the risk of associated diseases. Periodontitis develops slowly, with irreversible damage occurring during active bursts of inflammation. Affected people are often unaware of the disease as it is not yet possible to accurately predict disease flare-ups.
Approach-Control of inflammation is complex and known to be fuelled by several proteins. Matrix metalloproteinases (MMPs) are enzymes that cut proteins to alter their functions, thus controlling the start and end of inflammation. With our unique methods that identify cut protein ends, we discovered that many pro-inflammatory proteins are cut by MMPs. Thus, by trimming inflammatory proteins and their regulators, MMPs orchestrate inflammation.
We will study how cutting changes the actions of bioactive molecules in gingivitis, e.g., determine if trimming dampens or worsens inflammation and if male and female patients show differences that could influence treatment. We will make tools based on the cut ends to measure intact and cut molecules in healthy vs. inflamed human periodontium and will use these to assess if these cut ends can be used to monitor inflammation.
Impact-Our study will help unravel new complexity in inflammation control in human tissues using gingivitis as a model. Our results will identify new drug targets and, in the future, potentially new tests for earlier diagnosis of inflammatory diseases.
Programme
Project Grant - Priority Announcement: IMHA: Oral Health
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
484000
Name
Overall Christopher M
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Musculoskeletal Health and Arthritis
Theme2
Biomedical
Prcname2
Clinical Investigation - B: Arthritis, Bone, Skin and Cartilage
Projecttitle
Acute human gingivitis systems biology
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$100,000
Cihrequipment2
$0
Programname2
Project Grant - Priority Announcement: IMHA: Oral Health
Keyworddelim
Biomarkers; Gingiva; Gingivitis; Inflammatory Diseases; Mmps; Pericoronitis; Periodontium; Proteases; Proteomics; Serpins
Abstract
.
Significance-Inflammation is the body's protective response to infection. Inflammation normally turns off to allow healing. Prolonged inflammation results in diseases, e.g., gingivitis, periodontitis, arthritis and fibrosis. Gingivitis (mild gum inflammation) can progress to severe periodontitis to ultimately cause jaw bone and tooth loss. Periodontal disease is common-in the US, 47% of adults >30 years have gum disease, rising to 70% at >65 years-and is associated with an increased risk of other serious conditions, e.g. diabetes, heart attack and rheumatoid arthritis. Thus, preventing periodontitis reduces the risk of associated diseases. Periodontitis develops slowly, with irreversible damage occurring during active bursts of inflammation. Affected people are often unaware of the disease as it is not yet possible to accurately predict disease flare-ups.
Approach-Control of inflammation is complex and known to be fuelled by several proteins. Matrix metalloproteinases (MMPs) are enzymes that cut proteins to alter their functions, thus controlling the start and end of inflammation. With our unique methods that identify cut protein ends, we discovered that many pro-inflammatory proteins are cut by MMPs. Thus, by trimming inflammatory proteins and their regulators, MMPs orchestrate inflammation.
We will study how cutting changes the actions of bioactive molecules in gingivitis, e.g., determine if trimming dampens or worsens inflammation and if male and female patients show differences that could influence treatment. We will make tools based on the cut ends to measure intact and cut molecules in healthy vs. inflamed human periodontium and will use these to assess if these cut ends can be used to monitor inflammation.
Impact-Our study will help unravel new complexity in inflammation control in human tissues using gingivitis as a model. Our results will identify new drug targets and, in the future, potentially new tests for earlier diagnosis of inflammatory diseases.
Competitiondate
202303
Approvedterm2
1 yr 0 mth
Pinamesdelim
Overall, Christopher M
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $100,000~ $0~