Fetuin-A, Type 2 Diabetes, and Risk of Cardiovascular Disease in Older Adults

Author:

Jensen Majken K.1,Bartz Traci M.2,Mukamal Kenneth J.3,Djoussé Luc4,Kizer Jorge R.5,Tracy Russell P.6,Zieman Susan J.7,Rimm Eric B.18,Siscovick David S.9,Shlipak Michael10,Ix Joachim H.11

Affiliation:

1. Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts

2. Department of Biostatistics, University of Washington, Seattle, Washington

3. Beth Israel Deaconess Medical Center, Boston, Massachusetts

4. Division of Aging, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts and Boston Veterans Affairs Healthcare System, Boston, Massachusetts

5. Departments of Medicine and Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York

6. Department of Pathology, Colchester Research Facility, University of Vermont, Colchester, Vermont

7. National Institute on Aging, National Institutes of Health, Bethesda, Maryland

8. Channing Division of Network Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts

9. Cardiovascular Health Research Unit, Departments of Medicine and Epidemiology, University of Washington, Seattle, Washington

10. Division of General Internal Medicine, San Francisco Veterans Affairs Medical Center and Departments of Medicine, Epidemiology, and Biostatistics, University of California, San Francisco, San Francisco, California

11. Nephrology Section, Veterans Affairs San Diego Healthcare System, and Divisions of Nephrology and Preventive Medicine, University of California, San Diego, San Diego, California

Abstract

OBJECTIVE Fetuin-A, a hepatic secretory protein that simultaneously inhibits arterial calcification and insulin action, is associated with type 2 diabetes, but its association with cardiovascular disease (CVD) is uncertain. Preliminary studies suggest that the association of fetuin-A with CVD might differ among individuals with or without type 2 diabetes. RESEARCH DESIGN AND METHODS This was a prospective study of 3,810 community-living individuals older than 65 years (511 with type 2 diabetes) and free of CVD in 1992 when fetuin-A levels were measured. Participants were followed-up for incident CVD through June 2008. RESULTS Mean age was 75 years, and 61% were women; 1,456 participants had an incident CVD event (248 among individuals with type 2 diabetes). The association of fetuin-A with CVD was modified by type 2 diabetes (P interaction = 0.02). Higher fetuin-A was associated with lower CVD risk among persons without type 2 diabetes [hazard ratio per SD 0.1 g/L higher fetuin-A, 0.93 (95% CI, 0.88–0.99)], whereas a trend in the opposite direction was observed among individuals with type 2 diabetes, although it was not statistically significant [1.07 (0.93–1.22)]. Among individuals without type 2 diabetes, similar effect modification was observed by obesity and insulin resistance. Consistently, higher fetuin-A was associated with lower CVD risk only in the subgroups without obesity or with HOMA-IR below the median [0.91 (0.85–0.97) and 0.87 (0.79–0.95), respectively]. CONCLUSIONS The association of fetuin-A with risk of CVD differs among elderly individuals with and without insulin resistance or type 2 diabetes.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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