Donate Help Contact The AHA Sign In Home
American Heart Association
Arteriosclerosis, Thrombosis, and Vascular Biology
Search: search_blue_button Advanced Search
Arteriosclerosis, Thrombosis, and Vascular Biology. 2006;26:1086-1093
Published online before print March 2, 2006, doi: 10.1161/01.ATV.0000215951.36219.a4
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Data Supplement
Right arrow All Versions of this Article:
26/5/1086    most recent
01.ATV.0000215951.36219.a4v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by de Jager, J.
Right arrow Articles by Stehouwer, C. D.A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by de Jager, J.
Right arrow Articles by Stehouwer, C. D.A.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Medline Plus Health Information
*Diabetes
Hazardous Substances DB
*GLUCOSE
(Arteriosclerosis, Thrombosis, and Vascular Biology. 2006;26:1086.)
© 2006 American Heart Association, Inc.


Vascular Biology

Endothelial Dysfunction and Low-Grade Inflammation Explain Much of the Excess Cardiovascular Mortality in Individuals With Type 2 Diabetes

The Hoorn Study

Jolien de Jager; Jacqueline M. Dekker; Adriaan Kooy; Piet J. Kostense; Giel Nijpels; Rob J. Heine; Lex M. Bouter; Coen D.A. Stehouwer

From the Department of Internal Medicine, Bethesda General Hospital, Hoogeveen, the Netherlands (J.d.J., A.K); the Institute for Research in Extramural Medicine (J.M.D., P.J.K., G.N., R.J.H., L.M.B., C.D.A.S.), VU University Medical Center, Amsterdam, The Netherlands; and the Department of Internal Medicine, University Hospital Maastricht, The Netherlands (C.D.A.S.).

Correspondence to Coen D.A. Stehouwer, MD, Professor and Chair, Department of Medicine, University Hospital Maastricht, PO Box 5800, 6202 AZ Maastricht, The Netherlands. E-mail csteh{at}sint.azm.nl

Objective— The mechanisms responsible for the increased cardiovascular disease risk that accompanies type 2 diabetes (T2D) remain poorly understood. It is commonly held that endothelial dysfunction and low-grade inflammation can explain, at least in part, why deteriorating glucose tolerance is associated with cardiovascular disease. However, there is no direct evidence for this contention.

Methods and Results— In this population-based study (n=631), T2D was cross-sectionally associated with both endothelial dysfunction and low-grade inflammation, whereas impaired glucose metabolism (IGM) was associated only with low-grade inflammation. These findings were independent of other risk factors that accompany T2D or IGM. During a follow-up of 11.7 years (median; range 0.5 to 13.2 years), low-grade inflammation was associated with a greater risk of cardiovascular mortality (hazard ratio, 1.43 [95% CI, 1.17 to 1.77] per 1 SD difference). For endothelial dysfunction, the association with cardiovascular mortality was stronger in diabetic (hazard ratio, 1.87 [95% CI, 1.43 to 2.45]) than in nondiabetic individuals (hazard ratio, 1.23 [95% CI, 0.86 to 1.75]; P interaction=0.06). Finally, T2D-associated endothelial dysfunction and low-grade inflammation explained {approx}43% of the increase in cardiovascular mortality risk conferred by T2D.

Conclusions— These data emphasize the necessity of randomized controlled trials of strategies that aim to decrease cardiovascular disease risk by improving endothelial function and decreasing low-grade inflammation, especially for T2D patients.

Endothelial dysfunction and low-grade inflammation may explain, at least in part, the increased cardiovascular disease risk in type 2 diabetes (T2D). For endothelial dysfunction, the association with cardiovascular mortality was stronger in diabetic than in nondiabetic individuals (P interaction=0.06). T2D-associated endothelial dysfunction and low-grade inflammation explained {approx}43% of the increase in cardiovascular mortality risk conferred by T2D.


Key Words: epidemiology • diabetes mellitus • endothelium • inflammation • mortality




This article has been cited by other articles:


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
K. S. Stamatelopoulos, G. D. Kitas, C. M. Papamichael, E. Chryssohoou, K. Kyrkou, G. Georgiopoulos, A. Protogerou, V. F. Panoulas, A. Sandoo, N. Tentolouris, et al.
Atherosclerosis in Rheumatoid Arthritis Versus Diabetes: A Comparative Study
Arterioscler Thromb Vasc Biol, October 1, 2009; 29(10): 1702 - 1708.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
R. B. Goldberg
Cytokine and Cytokine-Like Inflammation Markers, Endothelial Dysfunction, and Imbalanced Coagulation in Development of Diabetes and Its Complications
J. Clin. Endocrinol. Metab., September 1, 2009; 94(9): 3171 - 3182.
[Abstract] [Full Text] [PDF]


Home page
Arch Intern MedHome page
A. Kooy, J. de Jager, P. Lehert, D. Bets, M. G. Wulffele, A. J. M. Donker, and C. D. A. Stehouwer
Long-term Effects of Metformin on Metabolism and Microvascular and Macrovascular Disease in Patients With Type 2 Diabetes Mellitus
Arch Intern Med, March 23, 2009; 169(6): 616 - 625.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
A. B. M. Reddy, K. V. Ramana, S. Srivastava, A. Bhatnagar, and S. K. Srivastava
Aldose Reductase Regulates High Glucose-Induced Ectodomain Shedding of Tumor Necrosis Factor (TNF)-{alpha} via Protein Kinase C-{delta} and TNF-{alpha} Converting Enzyme in Vascular Smooth Muscle Cells
Endocrinology, January 1, 2009; 150(1): 63 - 74.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
M. Xue, Q. Qian, A. Adaikalakoteswari, N. Rabbani, R. Babaei-Jadidi, and P. J. Thornalley
Activation of NF-E2-Related Factor-2 Reverses Biochemical Dysfunction of Endothelial Cells Induced by Hyperglycemia Linked to Vascular Disease
Diabetes, October 1, 2008; 57(10): 2809 - 2817.
[Abstract] [Full Text] [PDF]


Home page
Diabetes CareHome page
A. S. Astrup, L. Tarnow, L. Pietraszek, C. G. Schalkwijk, C. D.A. Stehouwer, H.-H. Parving, and P. Rossing
Markers of Endothelial Dysfunction and Inflammation in Type 1 Diabetic Patients With or Without Diabetic Nephropathy Followed for 10 Years: Association with mortality and decline of glomerular filtration rate
Diabetes Care, June 1, 2008; 31(6): 1170 - 1176.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
J. P. Corsetti, D. Ryan, A. J. Moss, D. L. Rainwater, W. Zareba, and C. E. Sparks
Glycoprotein Ib{alpha} Polymorphism T145M, Elevated Lipoprotein-Associated Phospholipase A2, and Hypertriglyceridemia Predict Risk for Recurrent Coronary Events in Diabetic Postinfarction Patients
Diabetes, May 1, 2007; 56(5): 1429 - 1435.
[Abstract] [Full Text] [PDF]