Risk Factors for First and Subsequent CVD Events in Type 1 Diabetes: The DCCT/EDIC Study

Author:

Bebu Ionut1ORCID,Schade David2ORCID,Braffett Barbara1ORCID,Kosiborod Mikhail34ORCID,Lopes-Virella Maria5ORCID,Soliman Elsayed Z.6ORCID,Herman William H.7ORCID,Bluemke David A.8,Wallia Amisha9ORCID,Orchard Trevor10,Lachin John M.1ORCID

Affiliation:

1. Biostatistics Center, The George Washington University, Rockville, MD

2. The University of New Mexico, Albuquerque, NM

3. Saint Luke’s Mid America Heart Institute and University of Missouri–Kansas City, Kansas City, MO

4. The George Institute for Global Health, University of New South Wales, Sydney, New South Wales, Australia

5. Department of Medicine, Medical University of South Carolina, Charleston, SC

6. School of Medicine, Wake Forest University, Winston-Salem, NC

7. Schools of Medicine and Public Health, University of Michigan, Ann Arbor, MI

8. Department of Radiology, University of Wisconsin School of Medicine and Public Health, Madison, WI

9. Department of Medicine, Northwestern University, Evanston, IL

10. University of Pittsburgh, Pittsburgh, PA

Abstract

OBJECTIVE The Diabetes Control and Complications Trial (DCCT) and its observational follow-up Epidemiology of Diabetes Interventions and Complications (EDIC) demonstrated the dominant role of glycemia, second only to age, as a risk factor for a first cardiovascular event in type 1 diabetes (T1D). We now investigate the association between established risk factors and the total cardiovascular disease (CVD) burden, including subsequent (i.e., recurrent) events. RESEARCH DESIGN AND METHODS CVD events in the 1,441 DCCT/EDIC participants were analyzed separately by type (CVD death, acute myocardial infarction [MI], stroke, silent MI, angina, percutaneous transluminal coronary angioplasty/coronary artery bypass graft [PTCA/CABG], and congestive heart failure [CHF]) or as composite outcomes (CVD or major adverse cardiovascular events [MACE]). Proportional rate models and conditional models assessed associations between risk factors and CVD outcomes. RESULTS Over a median follow-up of 29 years, 239 participants had 421 CVD events, and 120 individuals had 149 MACE. Age was the strongest risk factor for acute MI, silent MI, stroke, and PTCA/CABG, while glycemia was the strongest risk factor for CVD death, CHF, and angina, second strongest for acute MI and PTCA/CABG, third strongest for stroke, and not associated with silent MI. HbA1c was the strongest modifiable risk factor for a first CVD event (CVD: HR 1.38 [95% CI 1.21, 1.56] per 1% higher HbA1c; MACE: HR 1.54 [1.30, 1.82]) and also for subsequent CVD events (CVD: incidence ratio [IR] 1.28 [95% CI 1.09, 1.51]; MACE: IR 1.89 [1.36, 2.61]). CONCLUSIONS Intensive glycemic management is recommended to lower the risk of initial CVD events in T1D. After a first event, optimal glycemic control may reduce the risk of recurrent CVD events and should be maintained.

Funder

National Institute of Diabetes and Digestive and Kidney Disease

Publisher

American Diabetes Association

Subject

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

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