Risk Factors Related to Inflammation and Endothelial Dysfunction in the DCCT/EDIC Cohort and Their Relationship With Nephropathy and Macrovascular Complications

Publication Description
Risk Factors Related to Inflammation and Endothelial Dysfunction in the DCCT/EDIC Cohort and Their Relationship With Nephropathy and Macrovascular Complications Maria F. Lopes-Virella , MD, PHD 1 , Rickey E. Carter , PHD 2 , Gregory E. Gilbert , MS 2 , Richard L. Klein , PHD 1 , Miran Jaffa , PHD 2 , Alicia J. Jenkins , MD 1 3 , Timothy J. Lyons , MD 1 3 , W. Timothy Garvey , MD 1 4 , Gabriel Virella , MD, PHD 5 and and the DCCT/EDIC Cohort Study Group 1 Department of Medicine and Laboratory Services, Medical University of South Carolina and Ralph H. Johnson VA Medical Center, Charleston, South Carolina 2 Department of Biostatistics, Bioinformatics, and Epidemiology, Medical University of South Carolina, Charleston, South Carolina 3 Section of Endocrinology, Oklahoma University of Health Sciences Center, Oklahoma City, Oklahoma 4 Department of Nutrition, University of Alabama, Birmingham, Alabama 5 Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, South Carolina Corresponding author: Maria F. Lopes-Virella, virellam{at}musc.edu Abstract OBJECTIVE —Because endothelial cell dysfunction and inflammation are key contributors to the development of complications in type 1 diabetes, we studied risk factors related to endothelial dysfunction and inflammation (C-reactive protein and fibrinogen, soluble vascular cell adhesion molecule-1, intracellular adhesion molecule-1, and E-selectin, and fibrinolytic markers) in a subgroup of patients from the Diabetes Control and Complications Trial (DCCT)/Epidemiology of Diabetes Intervention and Complications (EDIC) study cohort. RESEARCH DESIGN AND METHODS —We determined which of these risk factors or clusters thereof are associated with the presence of and subsequent development of nephropathy and macrovascular complications (reflected by carotid intima-media thickness [IMT]). RESULTS —After adjustment for conventional risk factors (age, sex, DCCT treatment group, diabetes duration, A1C, systolic blood pressure, waist-to-hip ratio, total and HDL cholesterol, and smoking status), fibrinogen remained strongly associated with progression of internal and common carotid IMT ( P < 0.01) and soluble E-selectin had a strong association with nephropathy ( P < 0.01). CONCLUSIONS —The best predictor for IMT progression in the DCCT/EDIC cohort was plasma fibrinogen, and the levels of soluble E-selectin discriminate patients with albuminuria better than conventional risk factors. Footnotes Published ahead of print at http://care.diabetesjournals.org on 15 July 2008. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details. 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 July 10, 2008. Received April 3, 2008. DIABETES CARE

Primary Author
Maria F. Lopes-Virella
Rickey E. Carter
Gregory E. Gilbert
Richard L. Klein
Miran Jaffa
Alicia J. Jenkins
Timothy J. Lyons
W. Timothy Garvey
Gabriel Virella

Volume
31

Issue
10

Start Page
2006

Other Pages
2012

Publisher
American Diabetes Association

URL
http://care.diabetesjournals.org/content/31/10/2006.abstract

PMID
18628568

PMCID
PMC2551645



Reference Type
Journal Article

Periodical Full
Diabetes Care

Publication Year
2008

Publication Date
Oct 1,

Place of Publication
United States

ISSN/ISBN
0149-5992

Document Object Index
10.2337/dc08-0659