Author/Editor     Stegnar, M; Peternel, P; Uhrin, P; Cvelbar-Marinko, T; Goršič-Tomažič, K; Binder, BR
Title     Fibrinolysis in patients with the 1691 G-A mutation in factor V gene and history of deep vein thrombosis
Type     članek
Source     Fibrinolysis Proteolysis
Vol. and No.     Letnik 11, št. 4
Publication year     1997
Volume     str. 201-7
Language     eng
Abstract     It was observed that cosegregation of two inherited risk factors for deep vein thrombosis (DVT), e.g. resistance to activated protein C (APC) with protein C or protein S deficiency increases clinical manifestation of DVT. The aim was to establish if there exists cosegreagtaion of the 1691 G-A mutation in factor V gene, the major cause of resistance to APC and impairment of fibrinolysis, and if possible cosegregation of both defects effects severity of the disease. Eighty-eight consecutive patients (37 females, 51 males, aged 19-60, mean 42 years) were investigated 18 +- 10 months after acute DVT. In 15 patients (16%), the 1691 G-A mutation in factor V gene was observed. These patients did not differ from other DVT patients by clinical characteristics, age, body mass index, fasting glucose and cholesterol, or by resting levels of tissue-type plasminogen activator (t-PA), plasminogen activator inhibitor 1 (PAI-1) and euglobulin activity (t-PA antigen: 7.5 vs 7.1 ng/mL; t-PA activity: 0.9 IU/mL; PAI-1 antigen: 18.1 vs 13.6 ng/mL; PAI activity 13.8 vs 13.9 IU/mL, all values medians; euglobulin clot lysis time: 308 +- 32 vs 298 +- 78 min, mean +- SD). Moreover, frequncies of abnormal levels of t-PA, PAI-1 (t-PA antigen > 13 ng/mL, t-PA activity < 0.1 IU/mL, PAI-1 antigen > 37 ng/mL, PAI activity > 35 IU/mL) and euglobulin activity (euglobulin clot lysis time > 410 min) were similar in both subgroups of patients. Recurrent DVT was not more frequent in patients with both defectsL the 1691 G-A mutation in factor V gene and impared fibrinolysis. It was concluded that altered fibrinolysis is not an aggrevating factor for DVT in patients with the 1691 G-A mutation in factor V gene.
Descriptors     THROMBOPHLEBITIS
FIBRINOLYSIS
FACTOR V
PROTEIN C
PROTEIN S
BODY MASS INDEX
CHOLESTEROL
ALTEPLASE
PLASMINOGEN ACTIVATOR INHIBITOR 1
POLYMERASE CHAIN REACTION