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Grant: CIHR Fellowship

Direct Payment

$225,000.00

Composite biomarkers to untangle resident cell aging trajectories in sarcopenia

EF 2024-25

Résumé
The decline in skeletal muscle mass and strength in old age is a chronic disease defined as sarcopenia, and it is a major determinant of quality of life and independent loss. To date, it is unclear how molecular changes to the cells within the tissue contribute to muscle weakness, and whether some cell populations are particularly vulnerable or why. An important advance in the field of aging research has been the development of machine learning algorithms that can evaluate the aging signature of a biological sample. Recently, our group has developed such a tool that is compatible with single-cell gene expression data (transcriptomics). The goal of this current project is to adapt the framework and learn the signatures associated with age-induced muscle weakness, essentially using transcriptomics data as composite biomarkers. This will subsequently enable the analysis of human sarcopenia at the cellular level. The biomarkers developed here will yield a greater understanding of sarcopenia onset and will be of high therapeutic value when evaluating new or existing interventions for prolonging healthy muscle function in the elderly.
Programme
CIHR Fellowship
Bénéficiaire
Emplacement
Massachusetts, United States of America
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
513503
Name
Jacques Erik
Region
Massachusetts
Country
United States of America
Orgtype
Research Institution
Instname2
Aging
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Composite biomarkers to untangle resident cell aging trajectories in sarcopenia
Programtype2
Fellowship Programs
Orgnameinp2
Direct Payment
Cihramount2
$225,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Aging Clocks; Sarcopenia; Single-Cell Omics; Skeletal Muscle
Abstract
The decline in skeletal muscle mass and strength in old age is a chronic disease defined as sarcopenia, and it is a major determinant of quality of life and independent loss. To date, it is unclear how molecular changes to the cells within the tissue contribute to muscle weakness, and whether some cell populations are particularly vulnerable or why. An important advance in the field of aging research has been the development of machine learning algorithms that can evaluate the aging signature of a biological sample. Recently, our group has developed such a tool that is compatible with single-cell gene expression data (transcriptomics). The goal of this current project is to adapt the framework and learn the signatures associated with age-induced muscle weakness, essentially using transcriptomics data as composite biomarkers. This will subsequently enable the analysis of human sarcopenia at the cellular level. The biomarkers developed here will yield a greater understanding of sarcopenia onset and will be of high therapeutic value when evaluating new or existing interventions for prolonging healthy muscle function in the elderly.
Competitiondate
202410
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Jacques, Erik
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $225,000~ $0~