APPARENT DIFFERENT THROMBOTIC TENDENCY IN PATIENTS WITH FACTOR-V LEIDEN AND PROTEIN-C DEFICIENCY DUE TO SELECTION OF PATIENTS

Citation
Rpm. Lensen et al., APPARENT DIFFERENT THROMBOTIC TENDENCY IN PATIENTS WITH FACTOR-V LEIDEN AND PROTEIN-C DEFICIENCY DUE TO SELECTION OF PATIENTS, Blood, 88(11), 1996, pp. 4205-4208
Citations number
14
Categorie Soggetti
Hematology
Journal title
BloodACNP
ISSN journal
00064971
Volume
88
Issue
11
Year of publication
1996
Pages
4205 - 4208
Database
ISI
SICI code
0006-4971(1996)88:11<4205:ADTTIP>2.0.ZU;2-4
Abstract
Both activated protein C (APC) resistance and protein C deficiency are associated with an increased risk for venous thrombosis. To assess th eir tendencies to venous thrombosis, we compared the median age of fir st venous thromboembolism in patients with factor V Leiden or protein C deficiency, who were identified either within unselected consecutive cases with a first deep venous thrombosis derived from a population-b ased case-control study, or identified by selection of patients with a deep venous thrombosis, who were referred for thrombophilia work-up. The median age of onset for 92 unselected APC resistant cases was 43 y ears and for 13 unselected protein C-deficient cases 47 years. The med ian age at the first thrombotic event for 28 APC-resistant members of thrombophilia families was 29 years and for 50 protein C-deficient mem bers of thrombophilia families 31.5 years. The median age of onset for all unselected patients (n = 105) was 45 years of age (range, 16 to 6 9 years) and the median age of onset for all selected patients from th e thrombophilia families (n = 78) was 30.5 years (range, 16 to 67 year s). These results show that within the case-control study and the fami ly studies, the median age of onset is very similar in patients with A PC resistance and patients with protein C deficiency. This suggests th at APC resistance is not less severe with respect to risk of thrombosi s than (heterozygous) protein C deficiency. In conclusion. the median age at which the first thrombosis occurs mainly depends on the way the patients are identified and not on the type of thrombophilia. (C) 199 6 by The American Society of Hematology.