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Background  Two variants in the gene encoding the cytochrome P450 2C9 enzyme ( CYP2C9 ) are considered the most significant genetic risk factors associated with bleeding after warfarin prescription. A variant in the vitamin K epoxide reductase ( VKORC1 ) has been also associated by several studies with warfarin response. Another variant in the P450 3A5 enzyme ( CYP3A5 ) gene is known to affect the metabolism of many drugs, including tacrolimus.    Findings  We conducted a population genetic study in 148 unrelated healthy Greek-Cypriot volunteers (through PCR-RFLP assays), in order to determine the frequencies of the above pharmacogenetics variants and to compare allele frequencies with those in other major ethnic groups. The allele frequencies of  CYP2C9*2, CYP2C9*3  and  CYP3A5*3  were found to be 0.162, 0.112 and 0.943 respectively, whereas  VKORC1  - 1639A was 0.534. The latter frequency differs significantly when compared with Caucasians, Asians and Africans (p < 0.001) and is still significant when compared with the geographically and culturally closely related to Greek-Cypriots, Hellenes of Greece (p = 0.01). Interestingly ~18% of our population are carriers of four or three risk alleles regarding warfarin sensitivity, therefore they have a high predisposition for bleeding after taking high or even normal warfarin doses.    Conclusions  Our data show no significant difference in the frequency of  CYP2C9  and  CYP3A5  allelic variants when compared to the Caucasian population, but differ significantly when compared with Africans and Asians (p < 0.001). Also, the frequency of variant  VKORC1  - 1639A differs between Greek-Cypriots and every other population we compared. Finally, about 1/5 Greek-Cypriots carry three or four risk alleles and ~50% of them carry at least two independent risk alleles regarding warfarin sensitivity, a potentially high risk for over-anticoagulation.

Genetic polymorphisms in warfarin and tacrolimus-related genes VKORC1, CYP2C9 and CYP3A5 in the Greek-Cypriot population