The Effect of Intensive Glycemic Treatment on Coronary Artery Calcification in Type 1 Diabetic Participants of the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Study

Publication Description
The Effect of Intensive Glycemic Treatment on Coronary Artery Calcification in Type 1 Diabetic Participants of the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Study Patricia A. Cleary 1 , Trevor J. Orchard 2 , Saul Genuth 3 , Nathan D. Wong 4 , Robert Detrano 5 , Jye-Yu C. Backlund 1 , Bernard Zinman 6 , Alan Jacobson 7 , Wanjie Sun 1 , John M. Lachin 1 , David M. Nathan 7 and for the DCCT/EDIC Research Group * 1 Biostatistics Center, George Washington University, Rockville, Maryland 2 University of Pittsburgh, Pittsburgh, Pennsylvania 3 Case Western Reserve University, Cleveland, Ohio 4 University of California, Irvine, California 5 Harbor UCLA (University of California, Los Angeles) Medical Center, Torrance, California 6 University of Toronto, Toronto, Canada 7 Harvard Medical School, Boston, Massachusetts Address correspondence to David M. Nathan MD, Diabetes Unit, Massachusetts General Hospital, 32 Fruit St., Boston, MA 02114-2698. E-mail: dnathan{at}partners.org . Reprint requests can be addressed to the DCCT/EDIC Research Group, Box NDIC/DCCT/EDIC, Bethesda, MD 20892 Abstract The Epidemiology of Diabetes Interventions and Complications (EDIC) study, an observational follow-up of the Diabetes Control and Complications Trial (DCCT) type 1 diabetes cohort, measured coronary artery calcification (CAC), an index of atherosclerosis, with computed tomography (CT) in 1,205 EDIC patients at ∼7–9 years after the end of the DCCT. We examined the influence of the 6.5 years of prior conventional versus intensive diabetes treatment during the DCCT, as well as the effects of cardiovascular disease risk factors, on CAC. The prevalences of CAC >0 and >200 Agatston units were 31.0 and 8.5%, respectively. Compared with the conventional treatment group, the intensive group had significantly lower geometric mean CAC scores and a lower prevalence of CAC >0 in the primary retinopathy prevention cohort, but not in the secondary intervention cohort, and a lower prevalence of CAC >200 in the combined cohorts. Waist-to-hip ratio, smoking, hypertension, and hypercholesterolemia, before or at the time of CT, were significantly associated with CAC in univariate and multivariate analyses. CAC was associated with mean HbA 1c (A1C) levels before enrollment, during the DCCT, and during the EDIC study. Prior intensive diabetes treatment during the DCCT was associated with less atherosclerosis, largely because of reduced levels of A1C during the DCCT. CAC, coronary artery calcification CT, computed tomography CVD, cardiovascular disease DCCT, Diabetes Control and Complications Trial EDIC, Epidemiology of Diabetes Interventions and Complications IMT, intima-media thickness ROC, receiver operating characteristics Footnotes * * A complete list of individuals and institutions participating in the DCCT/EDIC Research Group appears in the appendix . The Writing Group of the DCCT/EDIC Research Group takes responsibility for the contents of this article. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Accepted August 23, 2006. Received May 11, 2006. DIABETES

Primary Author
Cleary,Patricia A.
Orchard,Trevor J.
Genuth,Saul
Wong,Nathan D.
Detrano,Robert
Jye-Yu C. Backlund
Zinman,Bernard
Jacobson,Alan
Sun,Wanjie
Lachin,John M.
Nathan,David M.

Volume
55

Issue
12

Start Page
3556

Other Pages
3565

Publisher
American Diabetes Association

URL
http://diabetes.diabetesjournals.org/content/55/12/3556.abstract http://diabetes.diabetesjournals.org/content/55/12/3556.abstract



Reference Type
Journal Article

Periodical Full
Diabetes

Publication Year
2006

Publication Date
Dec 1,

Place of Publication
United States

ISSN/ISBN
0012-1797

Document Object Index
10.2337/db06-0653