The overall objective of this contract is to establish a population-based research registry for systemic sclerosis (scleroderma) in southeastern Michigan. The Contractor will identify all cases of systemic sclerosis, verify all diagnoses, establish a computer data base, provide a continuous update of the prevalence, incidence and mortality rates of scleroderma in this population, and establish prospectively the average annual mortality. As a major focus, the Contractor will establish a cohort of incident cases for early intervention trials, as well as for basic science and other clinical and epidemiological studies.

Project Start
1994-10-05
Project End
1999-10-04
Budget Start
1995-09-22
Budget End
1996-10-04
Support Year
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Wayne State University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Detroit
State
MI
Country
United States
Zip Code
48202
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Mayes, Maureen D (2003) Scleroderma epidemiology. Rheum Dis Clin North Am 29:239-54
Arnett, F C; Cho, M; Chatterjee, S et al. (2001) Familial occurrence frequencies and relative risks for systemic sclerosis (scleroderma) in three United States cohorts. Arthritis Rheum 44:1359-62
Mayes, M D; Giannini, E H; Pachman, L M et al. (1997) Connective tissue disease registries. Arthritis Rheum 40:1556-9