© 1996 British Society for Rheumatology
brief-report |
COAGULATION FACTOR V GENE MUTATION INCREASES THE RISK OF VENOUS THROMBOSIS IN BEHÇET'S DISEASE


,
*Division of Rheumatology, Department of Internal Medicine, Istanbul Medical School Istanbul
Department of Genetics, Institute for Experimental Medicine (DETAM), Istanbul University Istanbul
Department of Molecular Biology and Genetics, Faculty of Science, Bilkent University Ankara, Turkey
Correspondence to:
Correspondence to: A. G
l, Zuhuratbaba Mah. T
rkis Cad. No: 14/8, Bakirk
y, Istanbul 34740, Turkey
We investigated the prevalence of the coagulation factor V gene G1691A mutation in 64 patients with Behçet's disease (BD) and in 107 apparently healthy individuals. The mutation was present in the heterozygous state in 37.5% of the patients with a history of deep vein thrombosis (12/32) and in 9.4% of the patients without any thrombotic event (3/32). Eleven healthy individuals were also heterozygous for the mutation (10.3%). The prevalence of the mutation in BD patients with and without thrombosis was significantly different (P = 0.0079). We conclude that the factor V gene mutation may play a major role in the development of venous thrombosis in BD.
KEY WORDS: Behcet's disease, Factor V gene mutation, Activated protein C resistance, Deep vein thrombosis, Vasculitis
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