Nasrollah Saleh-gohari - Genetic Department, Afzalipour School of Medicine, Kerman University of Medical Sciences, Kerman, Iran
Neda Salmani-Cheharfarsakhi - Genetic Laboratory, Afzalipour School of Medicine, Kerman University of Medical Sciences, Kerman, Iran

Background & Aims:Thromboembolism is an acute cardiovascular disease that ranges from clinically unimportant to massive embolism. Both acquired and hereditary risk factors contribute to the disease.
We aimed to determine the prevalence of two hereditary predisposing factor of the disease, prothrombin G۲۰۲۱۰A and factor V Leiden (G۱۶۹۱A) polymorphisms, in Kerman population. Methods:factor V and factor II genes of ۱۱۲ healthy individuals were examined to detect factor V Leiden (G۱۶۹۱A) and prothrombin G۲۰۲۱۰A variants. Genomic DNA of subjects was isolated from leukocytes of the whole blood using salt-saturation method. We used amplification refractory mutation system technique to find G۱۶۹۱A and G۲۰۲۱۰A variations. Results: We found two subjects with prothrombin G۲۰۲۱۰A mutation and three individuals with factor V Leiden variant, both in heterozygote state. The frequency of the polymorphisms were ۱.۷۹ and ۲.۶۸, respectively. No homozygote or compound heterozygote individual was detected for these two variants in this study. Conclusion: our findings about the polymorphisms frequency were different from what was detected in other provinces of Iran or in some region of neighboring countries. This discrepancy of the variant frequency can be explained by gene flow phenomenon.

Frequency, Factor V Leiden, Prothrombin G۲۰۲۱۰A