Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00035024.xml
Thromb Haemost 2002; 88(04): 694-697
DOI: 10.1055/s-0037-1613282
DOI: 10.1055/s-0037-1613282
Letters to the Editor
Genetic Risk Factors Associated with the Prognosis of Myocardial Infarction in Young Patients
Further Information
Publication History
Received
05 April 2002
Accepted after resubmission
29 May 2002
Publication Date:
09 December 2017 (online)
-
References
- 1 DeWood MA, Spores J, Notske RN. Prevalence of total coronary occlusion during the early hours of transmural myocardial infarction. N Engl J Med 1980; 303: 897-902.
- 2 Anderson JL, King GJ, Bair TL. et al. Associations between a polymorphism in the gene encoding glycoprotein IIIa and myocardial infarction and coronary artery disease. J Am Coll Cardiol 1999; 33: 727-33.
- 3 Margaglione M, Grandone E, Cappucci G. et al. An alternative method for PAI-1 promoter polymorphism (4G/5G) typing. Thromb Haemost 1997; 77: 605.
- 4 Green F, Kelleher C, Wilkes H. et al. A common genetic polymorphism associated with lower coagulation factor VII levels in healthy individuals. Arterioscler Thromb 1991; 11: 540-6.
- 5 Li YH, Chen JH, Tsai WC. et al. Synergistic effect of thrombomodulin promoter -33G/A polymorphism and smoking on the onset of acute myocardial infarction. Thromb Haemost 2002; 87: 86-91.
- 6 Frosst P, Blom HJ, Milos R. et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995; 10: 111-3.
- 7 Wang LX, Sim AS, Badenhop RF. et al. A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene. Nat Med 1996; 02: 41-5.
- 8 Tanaka S, Ohnoki S, Shibata H. et al. Gene frequencies of human platelet antigens on glycoprotein IIIa in Japanese. Transfusion 1996; 36: 813-7.
- 9 Hato T, Minamoto Y, Fukuyama T. et al. Polymorphisms of HPA-1 through 6 on platelet membrane glycoprotein receptors are not a genetic risk factor for myocardial infarction in the Japanese population. Am J Cardiol 1997; 80: 1222-4.
- 10 Herrmann SM, Poirier O, Marques-Vidal P. et al. The Leu33/Pro polymorphism (PlA1/PlA2) of the glycoprotein IIIa (GP IIIa) receptor is not related to myocardial infarction in the ECTIM study. Thromb Haemost 1997; 77: 1179-81.
- 11 Ridker PM, Hennekens CH, Schmitz C. et al. PlA1/A2 polymorphism of platelet glycoprotein IIIa and risks of myocardial infarction, stroke and venous thrombosis. Lancet 1997; 349: 385-8.
- 12 Ardissino D, Mannucci PM, Merlini PA. et al. Prothrombotic genetic risk factors in young survivors of myocardial infarction. Blood 1999; 94: 46-51.
- 13 Iwai N, Shimoike H, Nakamura Y. et al. The 4G/5G polymorphism of the plasminogen activator inhibitor gene is associated with the time course of progression to acute coronary syndromes. Atherosclerosis 1998; 136: 109-14.
- 14 Song J, Yoon YM, Jung HJ. et al. Plasminogen activator inhibitor-1 4G/5G promoter polymorphism and coagulation factor VII Arg353 → Gln polymorphism in Korean patients with coronary artery disease. J Korean Med Sci 2000; 15: 146-52.
- 15 Ye S, Green FR, Scarabin PY. et al. The 4G/5G genetic polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene is associated with differences in plasma PAI-1 activity but not with risk of myocardial infarction in the ECTIM study. Thromb Haemost 1995; 74: 837-41.
- 16 Ridker PM, Hennekens CH, Lindpaintner K. et al. Arterial and venous thrombosis is not associated with the 4G/5G polymorphism in the promoter of the plasminogen activator inhibitor gene in a large cohort of US men. Circulation 1997; 95: 59-62.
- 17 Tamaki S, Iwai N, Nakamura Y. et al. Variation of the factor VII gene and ischemic heart disease in Japanese subjects. Coronary Artery Disease 1999; 10: 601-6.
- 18 Lane A, Green F, Scarabin PY. et al. Factor VII Arg/Gln353 polymorphism determines factor VII coagulant activity in patients with myocardial infarction (MI) and control subjects in Belfast and in France but is not a strong indication of MI risk in ECTIM study. Atherosclerosis 1996; 119: 119-27.
- 19 Doggen CJM, Manger VCats, Bertina RM. et al. A genetic propensity to high factor VII is not associated with the risk of myocardial infarction in men. Thromb Haemost 1998; 80: 281-5.
- 20 Ireland H, Kunz G, Kyriakoulis K. et al. Thrombomodulin gene mutations associated with myocardial infarction. Circulation 1997; 96: 15-8.
- 21 Le Flem L, Picard V, Emmerich J. et al. Mutations in promoter region of thrombomodulin and venous thromboembolic disease. Arterioscler Thromb Vasc Biol 1999; 19: 1098-104.