Incidence of Factor V Leiden in Patients with Acute Myocardial Infarction
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作者:
Manohar S. Gowda
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机构:University of Missouri,Mid America Heart Institute and Department of Pathology
Manohar S. Gowda
Marjorie L. Zucker
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机构:University of Missouri,Mid America Heart Institute and Department of Pathology
Marjorie L. Zucker
James L. Vacek
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机构:University of Missouri,Mid America Heart Institute and Department of Pathology
James L. Vacek
William L. Carriger
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机构:University of Missouri,Mid America Heart Institute and Department of Pathology
William L. Carriger
Dana L. Van Laeys
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机构:University of Missouri,Mid America Heart Institute and Department of Pathology
Dana L. Van Laeys
Jane M. Rachel
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机构:University of Missouri,Mid America Heart Institute and Department of Pathology
Jane M. Rachel
Barbara D. Strope
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机构:University of Missouri,Mid America Heart Institute and Department of Pathology
Barbara D. Strope
机构:
[1] University of Missouri,Mid America Heart Institute and Department of Pathology
[2] St. Lukes Hospital,undefined
来源:
Journal of Thrombosis and Thrombolysis
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2000年
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9卷
关键词:
activated protein C resistance;
factor V Leiden;
myocardial infarction;
thrombosis;
D O I:
暂无
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学科分类号:
摘要:
The genetic defect of coagulation factor V known as factor V Leiden produces a resistance to degradation by activated protein C (APC) and increases the risk of venous thromboembolism. The data on arterial thrombosis associated with APC resistance are still not clearly defined. We conducted a study in patients presenting with acute myocardial infarction (MI) to assess whether factor V Leiden increases the risk of arterial thrombosis. We studied 109 patients who had a diagnosis of acute MI (69 males and 40 females, aged 25–91 years), and 112 controls. The study population was identified by characteristic ECG changes and elevation of serum CK-MB, whereas the control subjects were anonymous healthy blood donors with no known history of coronary artery disease. Blood samples from the patients and controls were analyzed for the factor V Leiden mutation by DNA analysis, using the polymerase chain reaction. Heterozygous factor V Leiden mutation was found in 9 of 109 (8%) MI patients and 5 of 112 (4%) control subjects (P = .42). In conclusion, this study shows no evidence of an association between factor V Leiden and acute MI.
机构:
Univ Birmingham, Dept Med, Rheumatol, Birmingham, W Midlands, EnglandUniv Birmingham, Dept Med, Rheumatol, Birmingham, W Midlands, England
Croft, A. P.
Khan, J. N.
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机构:
Univ Birmingham, Dept Med, Cardiol, Birmingham, W Midlands, EnglandUniv Birmingham, Dept Med, Rheumatol, Birmingham, W Midlands, England
Khan, J. N.
Chittari, M. V.
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机构:
Univ Birmingham, Dept Med, Cardiol, Birmingham, W Midlands, EnglandUniv Birmingham, Dept Med, Rheumatol, Birmingham, W Midlands, England
Chittari, M. V.
Varma, C.
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机构:
Univ Birmingham, Dept Med, Birmingham, W Midlands, England
City Hosp, Dept Cardiol, Birmingham, W Midlands, EnglandUniv Birmingham, Dept Med, Rheumatol, Birmingham, W Midlands, England
机构:
Calvary Mater Newcastle Hosp, Hunter Haematol Res Grp, Newcastle, NSW, Australia
Univ Newcastle, Sch Biomed Sci & Pharm, Callaghan, NSW 2308, AustraliaCalvary Mater Newcastle Hosp, Hunter Haematol Res Grp, Newcastle, NSW, Australia
Lincz, Lisa F.
Scorgie, Fiona E.
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机构:
Calvary Mater Newcastle Hosp, Hunter Haematol Res Grp, Newcastle, NSW, AustraliaCalvary Mater Newcastle Hosp, Hunter Haematol Res Grp, Newcastle, NSW, Australia
Scorgie, Fiona E.
Enjeti, Anoop
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机构:
Calvary Mater Newcastle Hosp, Hunter Haematol Res Grp, Newcastle, NSW, AustraliaCalvary Mater Newcastle Hosp, Hunter Haematol Res Grp, Newcastle, NSW, Australia
Enjeti, Anoop
Seldon, Michael
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机构:
Calvary Mater Newcastle Hosp, Hunter Haematol Res Grp, Newcastle, NSW, AustraliaCalvary Mater Newcastle Hosp, Hunter Haematol Res Grp, Newcastle, NSW, Australia