The Multipurpose Arthritis & Musculoskeletal Diseases Center at the University of North Carolina at Chapel Hill, chartered by the School of Medicine as the Thurston Arthritis Research Center, consists of a Biomedical Research Component, an Education, Epidemiology, & Health Services Research (E/E/HSR) Component, a Biomolecular Core, a Numerical Sciences Core, and an Administrative Unit. Ongoing Investigation in the Biomedical Research Component encompasses many of the issues relevant to autoimmunity, arthritis, and musculoskeletal disease: genetics, regulation, and function of recognition elements in normal and abnormal immune responses; peptide/MHC structure function relationships; induction and regulation of cytokine and inflammatory response genes; the repertoire of T cell receptor and B cell Ig genes and their role in autoimmunity; stem cell development; abnormal T cell activation and signal transduction in SLE; molecular genetics of autoantibody formation; contribution of autoantibodies to disease pathogenesis; immunosuppression; inciting agents in autoimmunity (bacterial cell walls, heat-shock proteins, mercury chloride); inflammation in experimental arthritis, and its therapy; biochemistry of osteoarthritis; experimental orthopaedics research; muscle metabolism; and clinical investigation. The Biomolecular Core will provide database support, DNA sequencing, flow cytometry, and mouse colony support for ongoing laboratory research. Three Developmental & Feasibility projects are proposed: 1) D&F project #1 involves basic studies on autoantibodies to phospholipids, which are associated with an increased risk of thrombosis, recurrent fetal loss, and thrombocytopenia; D&F project #2 proposes to clone and characterize a gene associated with a defect in muscle metabolism; D&F project #3 explores the role of IkappaB, an important regulatory element for induction of inflammatory genes, in SLE T cells. Areas of special emphasis in the E/E/HSR Component, which serves North Carolina and surrounding states, include: social and behavioral research, epidemiology of osteoarthritis, work disability, health promotion/disease prevention, health services research, arthritis in the elderly, and low back pain. Four E/E/HSR projects are proposed: project #1 entails a systematic examination and synthesis of novel behavioral science concepts as a means of developing an effective, efficient intervention strategy for patient education; project #2 examines the epidemiology of osteoarthritis and its influence on work force participation in minority and economically disadvantaged citizens; projects #3 and #4, respectively, will document the arthritis-related self-care behaviors of the elderly and examine the extent to which women approaching menopause recognize their increasing risk of osteoporosis and practice appropriate preventive behaviors. Support provided to the E/E/HSR Component by the Numerical Sciences Core includes: data entry, data management, programming, and consultation concerning research design, methodology, and data analysis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Comprehensive Center (P60)
Project #
2P60AR030701-12
Application #
3108243
Study Section
Arthritis and Musculoskeletal and Skin Diseases Special Grants Review Committee (AMS)
Project Start
1982-07-01
Project End
1998-06-30
Budget Start
1993-07-01
Budget End
1994-06-30
Support Year
12
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Medicine
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
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Qin, Jin; Barbour, Kamil E; Murphy, Louise B et al. (2017) Lifetime Risk of Symptomatic Hand Osteoarthritis: The Johnston County Osteoarthritis Project. Arthritis Rheumatol 69:1204-1212
An, H; Marron, J S; Schwartz, T A et al. (2016) Novel statistical methodology reveals that hip shape is associated with incident radiographic hip osteoarthritis among African American women. Osteoarthritis Cartilage 24:640-6

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