Should the factor V Leiden mutation be screened among ethnic Malays with venous thrombosis?

2010 ◽  
Vol 125 (5) ◽  
pp. 471-472 ◽  
Author(s):  
H.J. Ng ◽  
E.S. Koay ◽  
A. Abdul Ghafar ◽  
L.C. Lim ◽  
L.H. Lee
2006 ◽  
Vol 21 (1) ◽  
pp. 24-27 ◽  
Author(s):  
A Mansilha ◽  
F Araújo ◽  
M Severo ◽  
S M Sampaio ◽  
T Toledo ◽  
...  

Objective: To evaluate the association between the Factor V Leiden (FV R506Q) and prothrombin gene (FII G20210A) mutations and deep venous thrombosis (DVT) in young people. Methods: Blood samples were drawn from 199 subjects: 100 healthy controls and 99 unselected patients, with an objectively documented first episode of DVT under 40 years old. DNA analysis was performed using the polymerase chain reaction. Results: The mean age in the patient cohort was 27 years (range 16–40) and 68 (68.7%) were women. Patient prevalences were 20.6% and 10.1% for FV R506Q and FII G20210A, respectively. In the control group, carrier frequencies were 2% and 5%, respectively. We found an increased overall relative risk of DVT with statistical significance for FV R506Q carriers (OR: 12.8; 95% CI: 2.9–56.7; P < 0.001), but not for FII G20210A mutation (OR: 2.1; 95% CI: 0.7–6.5; P = 0.19). Conclusions: Our results suggest a possible increase in DVT risk for the young G20210A allele carriers, which can be more expressed in the presence of a circumstantial risk factor. There is extremely strong evidence that the Factor V Leiden mutation is an important risk factor in the development of a first episode of DVT in young people.


2004 ◽  
Vol 4 (1) ◽  
pp. 76-78
Author(s):  
Rouzbeh Chegeni . ◽  
Bahram Kazemi . ◽  
Abbas Hajifathali . ◽  
Aliakbar Pourfatholl . ◽  
Ghasem Rastegar Lari . ◽  
...  

2009 ◽  
Vol 57 (1) ◽  
pp. 91
Author(s):  
M Thomas ◽  
B George ◽  
J Mammen ◽  
S Aaron ◽  
M Alexander

2017 ◽  
Vol 37 (7) ◽  
pp. 963-964 ◽  
Author(s):  
Abass Awad-Elkareem ◽  
Salaheldein G. Elzaki ◽  
Hanan Khalid ◽  
Mual S. Abdallah ◽  
Ishag Adam

2002 ◽  
Vol 106 (4-5) ◽  
pp. 265-267 ◽  
Author(s):  
P Miljic ◽  
M Colovic ◽  
Lj Rakicevic ◽  
V Djordjevic ◽  
D Boskovic

Blood ◽  
1999 ◽  
Vol 93 (4) ◽  
pp. 1271-1276 ◽  
Author(s):  
Marieke C.H. de Visser ◽  
Frits R. Rosendaal ◽  
Rogier M. Bertina

Abstract Activated protein C (APC) resistance caused by the factor V Leiden mutation is associated with an increased risk of venous thrombosis. We investigated whether a reduced response to APC, not due to the factor V point mutation, is also a risk factor for venous thrombosis. For this analysis, we used the Leiden Thrombophilia Study (LETS), a case-control study for venous thrombosis including 474 patients with a first deep-vein thrombosis and 474 age- and sex-matched controls. All carriers of the factor V Leiden mutation were excluded. A dose-response relationship was observed between the sensitivity for APC and the risk of thrombosis: the lower the normalized APC sensitivity ratio, the higher the associated risk. The risk for the lowest quartile of normalized APC-SR (&lt;0.92), which included 16.5% of the healthy controls, compared with the highest quartile (normalized APC-SR &gt; 1.05) was greater than fourfold increased (OR = 4.4; 95% confidence interval, 2.9 to 6.6). We adjusted for VIII:C levels, which appeared to affect our APC resistance test. The adjusted (age, sex, FVIII:C) odds ratio for the lowest quartile was 2.5 (95% confidence interval, 1.5 to 4.2). So, after adjustment for factor VIII levels, a reduced response to APC remained a risk factor. Our results show that a reduced sensitivity for APC, not caused by the factor V Leiden mutation, is a risk factor for venous thrombosis.


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