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;26:845-850
Published online before print January 12, 2006, doi: 10.1161/01.ATV.0000203511.66681.7f
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Data Supplement
Right arrow All Versions of this Article:
26/4/845    most recent
01.ATV.0000203511.66681.7fv1
Right arrow Alert me when this article is cited
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 arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Meisner, F.
Right arrow Articles by Marx, N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Meisner, F.
Right arrow Articles by Marx, N.
Related Collections
Right arrow Other diabetes
Right arrow Other Treatment
Right arrow Other Vascular biology
Right arrow Pathophysiology
(Arteriosclerosis, Thrombosis, and Vascular Biology. 2006;26:845.)
© 2006 American Heart Association, Inc.


Vascular Biology

Effect of Rosiglitazone Treatment on Plaque Inflammation and Collagen Content in Nondiabetic Patients

Data From a Randomized Placebo-Controlled Trial

Franz Meisner; Daniel Walcher; Florence Gizard; Xaver Kapfer; Roman Huber; Anja Noak; Ludger Sunder-Plassmann; Helga Bach; Cornelia Haug; Max Bachem; Tatjana Stojakovic; Winfried März; Vinzenz Hombach; Wolfgang Koenig; Bart Staels; Nikolaus Marx

From the Department of Thoracic and Vascular Surgery (F.M., X.K., L.S.-P.), University of Ulm, Germany; Department of Internal Medicine II—Cardiology (D.W., A.N., H.B., V.H., W.K., N.M.), University of Ulm, Germany; UR545 INSERM (F.G., B.S.), Départment d’Athérosclérose, Université de Lille, France; 4Department of Neurology (R.H.), University of Ulm, Germany; Department of Clinical Chemistry (C.H., M.B.), University of Ulm, Germany; and Clinical Institute of Medical and Chemical Laboratory Diagnostics (T.S., W.M.), Medical University Graz, Austria.

Correspondence to Nikolaus Marx, MD, Department of Internal Medicine II–Cardiology, University of Ulm, Robert-Koch-Str. 8, D-89081 Ulm, Germany. E-mail nikolaus.marx{at}medizin.uni-ulm.de

Background— Therapeutic strategies to stabilize advanced arteriosclerotic lesions may prevent plaque rupture and reduce the incidence of acute coronary syndromes. Thiazolidinediones (TZDs), like rosiglitazone, are oral antidiabetic drugs with additional antiinflammatory and potential antiatherogenic properties. In a randomized, placebo-controlled, single-blind trial, we examined the effect of 4 weeks of rosiglitazone therapy on histomorphological characteristics of plaque stability in artery specimen of nondiabetic patients scheduled for elective carotid endarterectomy.

Methods and Results— A total of 24 nondiabetic patients with symptomatic carotid artery stenosis were randomly assigned to rosiglitazone (4 mg BID) or placebo in addition to standard therapy. In this population of nondiabetic patients, rosiglitazone treatment did not significantly change fasting blood glucose, fasting insulin, or lipid parameters. In contrast, rosiglitazone significantly reduced CD4-lymphocyte content as well as macrophage HLA-DR expression in the shoulder region, reflecting less inflammatory activation of these cells by lymphocyte interferon-{gamma}. Moreover, rosiglitazone significantly increased plaque collagen content (7.7±1.6% versus 3.7±0.7% of plaque area; P=0.036) compared with placebo, suggesting that TZD treatment may stabilize arteriosclerotic lesions. In addition, rosiglitazone reduced serum levels of 2 inflammatory arteriosclerosis markers: C-reactive protein and serum amyloid A.

Conclusions— Four weeks of treatment with rosiglitazone significantly reduces vascular inflammation in nondiabetic patients, leading to a more stable type of arteriosclerotic lesion.

The present randomized, placebo-controlled, single-blind trial demonstrates in nondiabetic patients scheduled for carotid endarterectomy that 4 weeks of treatment with rosiglitazone significantly reduces vascular inflammation, leading to a more stable type of arteriosclerotic lesion.


Key Words: plaque • thiazolidinediones • inflammation • collagen • diabetes




This article has been cited by other articles:


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
E. Rigamonti, C. Fontaine, B. Lefebvre, C. Duhem, P. Lefebvre, N. Marx, B. Staels, and G. Chinetti-Gbaguidi
Induction of CXCR2 Receptor by Peroxisome Proliferator-Activated Receptor {gamma} in Human Macrophages
Arterioscler. Thromb. Vasc. Biol., May 1, 2008; 28(5): 932 - 939.
[Abstract] [Full Text] [PDF]


Home page
Vasc MedHome page
A. S. Kelly, A. M. Thelen, D. R. Kaiser, J. M. Gonzalez-Campoy, and A. J. Bank
Rosiglitazone improves endothelial function and inflammation but not asymmetric dimethylarginine or oxidative stress in patients with type 2 diabetes mellitus
Vascular Medicine, November 1, 2007; 12(4): 311 - 318.
[Abstract] [PDF]


Home page
J. Nutr.Home page
H. Shen, R. MacDonald, D. Bruemmer, A. Stromberg, A. Daugherty, X.-a. Li, M. Toborek, and B. Hennig
Zinc Deficiency Alters Lipid Metabolism in LDL Receptor Deficient Mice Treated with Rosiglitazone
J. Nutr., November 1, 2007; 137(11): 2339 - 2345.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
B. Askari, J. E. Kanter, A. M. Sherrid, D. L. Golej, A. T. Bender, J. Liu, W. A. Hsueh, J. A. Beavo, R. A. Coleman, and K. E. Bornfeldt
Rosiglitazone Inhibits Acyl-CoA Synthetase Activity and Fatty Acid Partitioning to Diacylglycerol and Triacylglycerol via a Peroxisome Proliferator-Activated Receptor-{gamma}-Independent Mechanism in Human Arterial Smooth Muscle Cells and Macrophages
Diabetes, April 1, 2007; 56(4): 1143 - 1152.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
J. D. Brown and J. Plutzky
Peroxisome Proliferator Activated Receptors as Transcriptional Nodal Points and Therapeutic Targets
Circulation, January 30, 2007; 115(4): 518 - 533.
[Abstract] [Full Text] [PDF]