Skip Navigation

European Heart Journal 2001 22(1):96-101; doi:10.1053/euhj.2000.2123
Copyright © 2001 by the European Society of Cardiology.
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow References
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (29)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Schächinger, V.
Right arrow Articles by Zeiher, A.M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schächinger, V.
Right arrow Articles by Zeiher, A.M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

NADH/NADPH oxidase p22 phox gene polymorphism is associated with improved coronary endothelial vasodilator function

V. Schächingerf1, M.B. Britten, S. Dimmeler and A.M. Zeiher

Department of Internal Medicine, Division of Cardiology, J. W. Goethe-University, Frankfurt, Germany

revised January 10, 2000; accepted January 14, 2000

Abstract

Aims The NADH/NADPH oxidase system plays a central role in vascular superoxide anion production, which appears to cause coronary endothelial dysfunction. Recently, it has been suggested that the C242T polymorphism of the NADH/NADPH oxidase p22 phox gene can reduce susceptibility to coronary artery disease. We therefore tested whether this polymorphism is associated with an altered endothelium-dependent vasodilator capacity of human coronary arteries in vivo.

Methods and Results The vasodilator function of epicardial arteries in 93 patients was assessed by endothelium-mediated, flow-dependent dilation and nitroglycerin, which is endothelium-independent. NADH/NADPH oxidase p22 phox polymorphism was determined by restriction fragment length polymorphism. Carriers of the CC genotype of the C242T p22 phox polymorphism (n=44) revealed a significantly blunted endothelium-dependent dilator response (11±9·2% luminal area change vs 17±10%;P=0·007), which was, by multivariate analysis, independent of other risk factors or atherosclerosis itself. There was only a trend towards decreased endothelium-independent dilation in patients bearing the p22 phox CC genotype (P=0·07).

Conclusions The C242T polymorphism of the p22 phox gene is an important independent determinant of coronary endothelial vasodilator function. These results provide the first clinical evidence for the functional significance of a polymorphism of a gene related to superoxide anion production in the vascular wall.

Key Words: Risk factors, endothelial dysfunction, genes, free radicals, coronary artery disease

f1 Correspondence: Volker Schächinger, MD, Department of Internal Medicine, Division of Cardiology, J. W. Goethe-University, Theodor-Stern-kai 7, Germany


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
M. Arca, B. Conti, A. Montali, P. Pignatelli, F. Campagna, F. Barilla, G. Tanzilli, R. Verna, A. Vestri, C. Gaudio, et al.
C242T Polymorphism of NADPH Oxidase p22phox and Recurrence of Cardiovascular Events in Coronary Artery Disease
Arterioscler. Thromb. Vasc. Biol., April 1, 2008; 28(4): 752 - 757.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
K. Doi, E. Noiri, A. Nakao, T. Fujita, S. Kobayashi, and K. Tokunaga
Functional Polymorphisms in the Vascular Endothelial Growth Factor Gene Are Associated with Development of End-Stage Renal Disease in Males
J. Am. Soc. Nephrol., March 1, 2006; 17(3): 823 - 830.
[Abstract] [Full Text] [PDF]


Home page
HeartHome page
L C Jones and A D Hingorani
Genetic regulation of endothelial function
Heart, October 1, 2005; 91(10): 1275 - 1277.
[Full Text] [PDF]


Home page
Eur Heart JHome page
K. M Channon and H. Watkins
Coronary artery disease genetics: bigger is better
Eur. Heart J., June 1, 2004; 25(11): 900 - 901.
[Full Text] [PDF]


Home page
Diabetes CareHome page
R. Hayaishi-Okano, Y. Yamasaki, Y. Kajimoto, K.'y. Sakamoto, K. Ohtoshi, N. Katakami, D. Kawamori, T. Miyatsuka, M. Hatazaki, Y. Hazama, et al.
Association of NAD(P)H Oxidase p22 phox Gene Variation With Advanced Carotid Atherosclerosis in Japanese Type 2 Diabetes
Diabetes Care, February 1, 2003; 26(2): 458 - 463.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
G. Zalba, G. S. Jose, M. U. Moreno, M. A. Fortuno, A. Fortuno, F. J. Beaumont, and J. Diez
Oxidative Stress in Arterial Hypertension: Role of NAD(P)H Oxidase
Hypertension, December 1, 2001; 38(6): 1395 - 1399.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.