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Thromb Haemost 2010; 104(03): 650-652
DOI: 10.1160/TH10-01-0022
DOI: 10.1160/TH10-01-0022
Letters to the Editor
Synergism between factor XII –4C>T and factor XIII Val34Leu polymorphisms in fibrinolytic therapy in acute myocardial infarction
Financial support: Dr. Hernández-Romero holds a postdoctoral position funded by the Instituto de Salud Carlos III. This work was partially supported by RD06/0014/0039 (RECAVA).
Further Information
Publication History
Received:
08 January 2010
Accepted after minor revision:
17 April 2010
Publication Date:
23 November 2017 (online)
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References
- 1 Zeerleder S, Schloesser M, Redondo M. et al. Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency -a study on 73 subjects from 14 Swiss families. Thromb Haemost 1999; 82: 1240-1246.
- 2 Kanaji T, Okamura T, Osaki K. et al. A common genetic polymorphism (46 C to T substitution) in the 5’-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level. Blood 1998; 91: 2010-2014.
- 3 Millar GJ, Esnouf MP, Burgués AI. et al. Risk of coronary Heart disease and activation of factor XII in middle-aged men. Arterioscl Thromb Vac Biol 1997; 17: 2103-2106.
- 4 Zito F, Drummond F, Bujac S. et al. Epidemiological and genetic association of activated factor XII concentration with factor VII activity, fibrinopeptide A concentration, and risk of coronary heart disease in men. Circulation 2000; 102: 2058-2062.
- 5 Kohler HP, Futres TS, Grant PJ. FXII (46C->T) polymorphism and in vivo generation of FXII activity-gene frequencies and relationship in patients with coronary artery disease. Thromb Haemost 1999; 81: 745-747.
- 6 Zito F, Lowe GD, Rumley A. et al. WOSCOPS Study. Association of the factor XII 46 C->T polymorphism with risk of coronary heart disease in the WOSCOPS study. Atherosclerosis 2002; 165: 153-158.
- 7 Santamaría A, Mateo J, Tirado I. et al. Homozygosity of the T allele of the 46 C->T polymorphism in the F12 gene is a risk factor for ischemic stroke in spanish population. Stroke 2004; 35: 1795-1799.
- 8 Kleinschnitz C, Stoll G, Bendszus M. et al. Targeting coagulation factor XII provides protection form pathological thombosis in cerebral ischemia without interfering with hemostasis. J Exp Med 2006; 203: 513-518.
- 9 Müller F, Renné T. Novel roles for factor XII-driven plasma contact activation system. Curr Opin Hematol 2008; 15: 516-521.
- 10 Armstrong PW, Collen D. Fibrinolityc for acute myocardial infarction: current status and new horizons for pharmacological reperfusion, part 1. Circulation 2001; 103: 2862-2866.
- 11 Rallidis LS, Politou M, Komporozos C. et al. Factor XIII Val34Leu polymorphism and the risk of myocardial infarction under the age of 36 years. Thromb Haemost 2008; 99: 1085-1089.
- 12 Marín F, González-Conejero R, Lee KW. et al. A pharmacogenetic effect of factor XIII valine 34 Leucine polymorphism on fibrinolytic therapy for acute myocardial infarction. J Am Coll Cardiol 2005; 45: 25-29.
- 13 González-Conejero R, Fernández-Cadenas I, Iniesta JA. et al. for the Proyecto Ictus Research Group. Role of fibrinogen levels and factor XIII V34L polymorphism in thombolytic therapy in stroke patients. Stroke 2006; 37: 2288-2293.
- 14 Rader DJ, Puré E. Genetic Susceptibility to Atherosclerosis: Insights From Mice. Circ Res 2000; 86: 1013-1015.
- 15 Bergmann SR, Sobel BE. Noninvasive assessment of the efficacy of coronary thrombolysis. In: Thrombolysis in Cardiovascular Disease. New York, NY: Marcel Dekker; 1989. pp. 141-161.
- 16 Corral J, González-Conejero R, Iniesta JA. et al. The FXIII Val34Leu polymorphism in venous and arterial thromboembolism. Haematologica 2000; 85: 293-297.
- 17 Ariëns RAS, Philippou H, Nagaswami C. et al. The factor XIII V34L polymorphism accelerates thrombin activation of factor XIII and affects cross-linked fibrin structure. Blood 2000; 96: 988-995.
- 18 Cannon CP. Importance of TIMI 3 flow. Circulation 2001; 104: 624-627.
- 19 Gibson CM, Cannon CP, Murphy SA. et al., for the TIMI 10B Investigators. Relationship of TIMI myocardial perfusion grade to mortality following thrombolytic administration. Circulation 2000; 101: 125-130.
- 20 Syed MA, Borzak S, Asfour A. et al. Single lead ST-segment recovery: a simple, reliable measure of successful fibrinolysis after acute myocardial infarction. Am Heart J 2004; 147: 275-280.
- 21 Puleo PR, Perryman MB, Bresser MA. et al. Creatine kinase isoform analysis in the detection and assessment of thrombolysis in man. Circulation 1987; 75: 1162-1169.
- 22 Marín F, González-Conejero R, Capranzano P. et al. Pharmacogenetics in cardiovascular antithrombotic therapy. J Am Coll Cardiol 2009; 54: 1041-1057.