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PGP 2008-2009 | PGP 2009-2010 | PGP 2010-2011
SRP 2009-2010 | SRP 2010-2011
DAP: 2008 | 2009 | 2010 | 2011
PPG: 2008 | 2009 | 2010
SRI in OA 2003-2008 | SRI in IJD 2006-2011 | SRI in BIO 2008-2012
SRID: 2007-2008 | 2006-2007 | 2005-2006 | 2004-2005 | 2003-2005 | 2002-2004
Research Grants Awards
Research funding: 2004-2005
SRID - Inflammatory Joint Disease
SRID - Osteoarthritis
SRID - Restoration of Joint Function

SRID - Inflammatory Joint Disease
Biology and Outcomes in Spondyloarthriitis: a transdisciplinary
prospective multicentre study
Principal Investigator: Robert
Inman
Co-Principal Investigators:
D. Gladman, W. Maksymowych, P. Rahman,
M. Stone
Abstract
The prevalence of spondyloarthritis (SpA) approaches that
of rheumatoid arthritis, and the disability and economic
impact of these two chronic diseases is comparable. Despite
this, SpA has been comparatively underrepresented both in
terms of translational research and in the development of
effective biologic therapy. The current proposal represents
a collaborative initiative which links investigators into
an effective research network to apply state-of-the-art
methodologies of basic and clinical research to address
the important gaps in existing knowledge in SpA. The two
broad themes in this proposal will be (i) The biologic basis
of SpA. This will address the genetic basis of susceptibility
to the disease and of the expressed gene profile, the serological
assessment of disease activity and severity by cytokine
and biomarker measurements, and the immunological profile
of the disease. (ii) Clinical outcomes in SpA, This will
address clinical and radiographic outcomes to assess the
structural damage over time, the response to therapy and
the clinical burden of illness in terms of quality of life,
disability and socio-economic impact.

Disability while at work: A
comparison of different measures in
persons with arthritis.
Principal Investigator:
Claire Bombardier
Co-Principal Investigator:
D. Beaton, M. Gignac, D. Lacaille,
S. Solway
Abstract
Arthritis patients periodically miss days off work but also
may be less productive while at work. This study will compare
new approaches to measure self-reported "decreased
productivity at work". The results will provide guidance
on which measure is best suited to quantify work disability
in patients with arthritis and to help plan workplace interventions.
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SRID - Osteoarthritis
Risk factors that predict the
progression of osteoarthritis after
knee injury: A pilot project
Principal Investigator:
Mark Hurtig
Co-Principal Investigators:
M. Buschmann, J. Dickey, S Shirazi-Adl,
L. White, J. Wilkins
Abstract
The aim of this proposal is to identify factors that put
patients at risk of knee osteoarthritis (OA) after knee
injuries. The goal is to identify factors that predict which
patients need special, care such as medication, reconstructive
surgery, physiotherapy and counseling in order to prevent
or slow the progression of OA. Using mathematical modeling
and new diagnostic tests we will re-examine 60 patients
that had ACL and related injuries 5-6 years ago to determine
which patients are developing OA and why. This study would
identify patients who are at risk of developing OA after
knee injury, allowing our health care system to focus attention
and resources on those people who need them most.

Functional Genomics of Cartilage:
Molecular Approaches to identify novel
diagnostic and therapeutic targets
Principal Investigator:
Frank Beier
Co-Principal Investigators:
J. Aubin, J. Henderson, W. Stanford,
R. St-Arnaud, B. St-Jacques, M. Underhill
Abstract
Currently, only a few diagnostic markers or therapeutic
targets for the treatment of osteoarthritis are available.
We propose the comparative analyses of gene expression patterns
in several mutant mouse strains displaying severe cartilage
defects. These studies will result in the identification
of novel diagnostic and therapeutic targets in arthritis.

A model system for studying
the clearance of cartilage biomarkers
from normal and osteoarthritic joints
Principal Investigator:
John Matyas
Co-Principal Investigator:
Robin Poole
Abstract
A model system will study the clearance of biomarkers from
the joint into the systemic circulation in normal and osteoarthritic
joints. The rates of formation and disappearance biomarkers
will also be studied in the joint fluid, serum, and urine
after generating biomarkers in vitro and in vivo using enzymes
or transplanted cartilage (which disintegrates). The clearance
of biomarkers will be compared among normal knees, sham-operated
knees, and knees with experimental osteoarthritis.
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SRID - Restoration of Joint Function
Recombinant peptides for the
promotion of mineral formation
Principal Investigator: Harvey Goldberg
Co-Principal Investigators:
M. Buschmann, M. Grynpas, L. Gilles,
D. Holdsworth, G. Hunter, J. Sodek
Abstract
Loss of the bone supporting joints often occurs in rheumatoid
arthritis. A means of regenerating this bone would be of
great benefit to those with severe arthritis. We propose
to use bone sialoprotein, which we have previously shown
to be involved in bone mineralization, to induce new bone
formation in experimental animals.

Sheep stromal cells for cartilage tissue formation
Principal Investigator: William
Stanford
Co-Principal Investigators: J.
Aubin, M. Hurtig, R. Kandel, R. Pilliar
Abstract
To identify novel inhibitors that will effectively block
recruitment and activation of pro-inflammatory immune and
inflammatory cells in articular cartilage and the synovium.
In particular, we will study how the group of pro-inflammatory
mediators termed chemokines are proteolytically inactivated.
Our previous CAN funded work identified that tissue-degrading
enzymes (matrix metalloproteinases; MMPs) also efficiently
cleave chemokines to produce chemokine antagonists. This
heralds a potentially new class of anti-inflammatory agents
for the treatment of arthritis.

Functional integration of tissue-engineered ligaments
in situ post-grafting.
Principal Investigator: Francine
Goulet
Co-Principal Investigator: S.
Laverty
Abstract
The loss of a joint ligament leads to functional instability
and osteoarthritis. We successfully produced and grafted
a tissue-engineered ligament in the goat model. We now want
to assess our ligament integration in the dog since, like
humans, it often ruptures its ACL, and is therefore a suitable
clinical model.
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