Diabetes Care 30:1724-1729, 2007 DOI: 10.2337/dc07-0040 © 2007 by the American Diabetes Association
Elevated Cystatin C Concentration and Progression to Pre-DiabetesThe Western New York Study
1 Department of Social and Preventive Medicine, State University of New York at Buffalo, Buffalo, New York Address correspondence and reprint requests to Richard P. Donahue, PhD, MPH, Department of Social and Preventive Medicine, School of Public Health and Health Professions, State University of New York at Buffalo, 3435 Main St., Farber Hall, Room 268 F, Buffalo, NY 14214. E-mail: rpd1{at}buffalo.edu OBJECTIVE We conducted a nested case-control investigation to examine whether elevated baseline concentrations of cystatin C predicted progression from normoglycemia to pre-diabetes over 6 years of follow-up from the Western New York Health Study.
RESEARCH DESIGN AND METHODS In 20022004, 1,455 participants from the Western New York Health Study, who were free of type 2 diabetes and known cardiovascular disease at baseline (19962001), were reexamined. An incident case of pre-diabetes was defined as an individual with fasting glucose <100 mg/dl at the baseline examination and RESULTS Multivariate conditional logistic regression analyses adjusted for age, baseline glucose level, homeostasis model assessment of insulin resistance, BMI, hypertension, estimated glomerular filtration rate, cigarette smoking, and alcohol use revealed a significantly increased risk of progression to pre-diabetes among those with elevated baseline concentrations of cystatin C (odds ratio 3.28 [95% CI 1.437.54]) (upper quintile versus the remainder). Results of secondary analyses that considered high-sensitivity C-reactive protein, interleukin-6, E-selectin, or soluble intercellular adhesion molecule-1 did not alter these results. CONCLUSIONS These results suggest that cystatin C was associated with a threefold excess risk of progression to pre-diabetes in this population.
Abbreviations: ACR, albumin-to-creatinine ratio CVD, cardiovascular disease DPP, Diabetes Prevention Program eGFR, estimated glomerular filtration rate GFR, glomerular filtration rate hs-CRP, high-sensitivity C-reactive protein IL-6, interleukin-6 sE-selectin, soluble E-selectin HOMA-IR, homeostasis model assessment of insulin resistance IFG, impaired fasting glucose IGT, impaired glucose tolerance sICAM-1, soluble intercellular adhesion molecule-1
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