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. 1998;18:487-492

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
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 Schmidt, H.
Right arrow Articles by Kostner, G. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schmidt, H.
Right arrow Articles by Kostner, G. M.
(Arteriosclerosis, Thrombosis, and Vascular Biology. 1998;18:487-492.)
© 1998 American Heart Association, Inc.


Original Contributions

ß-Fibrinogen Gene Polymorphism (C148->T) Is Associated With Carotid Atherosclerosis

Results of the Austrian Stroke Prevention Study

Helena Schmidt; Reinhold Schmidt; Kurt Niederkorn; Susanne Horner; Peter Becsagh; Birgit Reinhart; Martin Schumacher; Viktor Weinrauch; ; Gert M. Kostner

From the Institute for Medical Biochemistry (H.S., P.B., G.M.K.) and the Departments of Neurology (R.S., K.N., S.H., B.R.) and Internal Medicine (M.S., V.W.), Karl-Franzens University, Graz, Austria.

Correspondence to Helena Schmidt, MD, Institute for Medical Biochemistry, Karl-Franzens University Graz, Harrachgasse 21, A-8010 Graz, Austria. E-mail helena.schmidt{at}kfunigraz.ac.at

Abstract—Polymorphisms at the ß-fibrinogen locus have been shown to be associated with plasma concentration of fibrinogen and coronary heart disease. The effect of the genetic heterogeneity of fibrinogen on carotid atherosclerosis has not been determined so far. We examined the influence of the C148->T polymorphism on carotid disease in a large cohort of middle-aged to elderly subjects without evidence of neuropsychiatric disease. This polymorphism is located close to the consensus sequence of the interleukin-6 element and may represent a functional sequence variant. The genotype of 399 randomly selected, neurologically asymptomatic individuals, aged 45 to 75 years, was determined by denaturing gradient gel electrophoresis. Carotid atherosclerosis was assessed by color-coded duplex scanning and was graded on a five-point scale ranging from 0 (=normal) to 5 (=complete luminal obstruction). The C/C, C/T, and T/T genotypes were noted in 226 (56.6%), 148 (37.1%), and 25 (6.3%) individuals, respectively. The T/T genotype group demonstrated higher grades of carotid atherosclerosis than did the C/C and C/T genotypes (P=.003). Logistic regression analysis created a model of independent predictors of carotid atherosclerosis that included apolipoprotein B (odds ratio [OR], 1.17/10 mg/dL), age (OR, 2.46/10 years), lifetime tobacco consumption (OR, 1.03/1000 g), presence of the ß-fibrinogen promoter T/T genotype (OR, 6.17), plasma fibrinogen concentration (OR, 1.05/10 mg/dL), and cardiac disease (OR, 1.80). These data suggest that the ß-fibrinogen promoter T/T148 genotype represents a genetic risk factor for carotid atherosclerosis in the middle-aged to elderly.


Key Words: fibrinogen • genetics • atherosclerosis • carotid arteries




This article has been cited by other articles:


Home page
StrokeHome page
M. Di Napoli and P. Singh
Is Plasma Fibrinogen Useful in Evaluating Ischemic Stroke Patients?: Why, How, and When
Stroke, May 1, 2009; 40(5): 1549 - 1552.
[Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
M P J van Goor, E B Gomez-Garcia, F W G Leebeek, G J Brouwers, P J Koudstaal, and D W J Dippel
The - 148 C/T fibrinogen gene polymorphism and fibrinogen levels in ischaemic stroke: a case-control study
J. Neurol. Neurosurg. Psychiatry, January 1, 2005; 76(1): 121 - 123.
[Abstract] [Full Text] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
T. A. Manolio, E. Boerwinkle, C. J. O'Donnell, and A. F. Wilson
Genetics of Ultrasonographic Carotid Atherosclerosis
Arterioscler Thromb Vasc Biol, September 1, 2004; 24(9): 1567 - 1577.
[Abstract] [Full Text] [PDF]


Home page
ChestHome page
J. B. Braunstein, D. W. Kershner, P. Bray, G. Gerstenblith, S. P. Schulman, W. S. Post, and R. S. Blumenthal
Interaction of Hemostatic Genetics With Hormone Therapy : New Insights To Explain Arterial Thrombosis in Postmenopausal Women
Chest, March 1, 2002; 121(3): 906 - 920.
[Abstract] [Full Text] [PDF]


Home page
Eur Heart JHome page
G.J. Blake, C. Schmitz, K. Lindpaintner, and P.M. Ridker
Mutation in the promoter region of the {beta}-fibrinogen gene and the risk of future myocardial infarction, stroke and venous thrombosis
Eur. Heart J., December 2, 2001; 22(24): 2262 - 2266.
[Abstract] [PDF]


Home page
J. Appl. Physiol.Home page
D. M. Herrington and K. P. Klein
Genome and Hormones: Gender Differences in Physiology: Invited Review: Pharmacogenetics of estrogen replacement therapy
J Appl Physiol, December 1, 2001; 91(6): 2776 - 2784.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
A. J. Catto
Genetic aspects of the hemostatic system in cerebrovascular disease
Neurology, September 1, 2001; 57(90002): S24 - 30.
[Abstract] [Full Text]


Home page
StrokeHome page
H. Schmidt, F. Fazekas, G. M. Kostner, C. M. van Duijn, and R. Schmidt
Angiotensinogen Gene Promoter Haplotype and Microangiopathy-Related Cerebral Damage : Results of the Austrian Stroke Prevention Study
Stroke, February 1, 2001; 32(2): 405 - 412.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
A. Hassan and H. S. Markus
Genetics and ischaemic stroke
Brain, September 1, 2000; 123(9): 1784 - 1812.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
D. A. Lane and P. J. Grant
Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease
Blood, March 1, 2000; 95(5): 1517 - 1532.
[Full Text] [PDF]


Home page
BloodHome page
S. O. Brennan, A. P. Fellowes, J. M. Faed, and P. M. George
Hypofibrinogenemia in an individual with 2 coding (gamma 82 Aright-arrowG and Bbeta 235 Pright-arrowL) and 2 noncoding mutations
Blood, March 1, 2000; 95(5): 1709 - 1713.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
H. Schmidt, R. Schmidt, K. Niederkorn, A. Gradert, M. Schumacher, N. Watzinger, H.-P. Hartung, and G. M. Kostner
Paraoxonase PON1 Polymorphism Leu-Met54 Is Associated With Carotid Atherosclerosis : Results of the Austrian Stroke Prevention Study
Stroke, October 1, 1998; 29(10): 2043 - 2048.
[Abstract] [Full Text] [PDF]