Key result
VKORC1 and CYP2C9 variants are linked to recurrent ischemic stroke in patients on acenocoumarol.
Why the study?
Variants in CYP2C9 and VKORC1 have been associated with acenocoumarol maintenance dose, but their association with stroke recurrence and intracranial haemorrhage in a Spanish population was unclear.
Are variants in VKORC1 and CYP2C9 associated with acenocoumarol maintenance dose, stroke recurrence, and intracranial haemorrhage in stroke patients?
Cohort (n=78)
Yes
Are variants in VKORC1 and CYP2C9 associated with acenocoumarol maintenance dose, stroke recurrence, and intracranial haemorrhage in stroke patients?
Genetic variants in VKORC1 and CYP2C9 are associated with acenocoumarol dosing requirements and clinical outcomes including stroke recurrence and intracranial haemorrhage.
Acenocoumarol is an oral anticoagulant with significant interindividual dose variations. Variants in CYP2C9 and VKORC1 have been associated with acenocoumarol maintenance dose. We analysed whether any of the 49 polymorphisms in CYP2C9 and VKORC1 previously associated with acenocoumarol maintenance dose in a Genome-Wide Association study (GWAs) in Dutch population are associated with stroke recurrence, intracranial haemorrhage (ICH) and acenocoumarol maintenance dose in a Spanish population. We performed a GWAs using Human Core Exome-chip (Illumina) in 78 patients stroke patients treated with acenocoumarol for secondary prevention enrolled as part of the prospective investigator-initiated study (IIS) SEDMAN Study. Patients were followed-up a median of 12.8 months. Three and eight patients had recurrent stroke and ICH events, respectively. We found 14 of the 49 published variants associated with acenocoumarol maintenance dose (p < 0.05). Six polymorphisms were associated with stroke recurrence and four variants with ICH (p < 0.05). In conclusion, variants in VKORC1 and CYP2C9 are associated with acenocoumarol maintenance dose, stroke recurrence and ICH in a Spanish cohort. These results highlight the relevance of studying pharmacogenetics associated with efficacy and safety of anticoagulant drugs and justify studies with larger sample size and different ethnic populations.
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Cullell et al. (2020) conducted a cohort in Cardioembolic stroke (n=78). VKORC1 and CYP2C9 polymorphisms was evaluated on Recurrence of symptomatic ischemic stroke (IS) (p=<0.05). Six genetic variants in VKORC1 and CYP2C9 were significantly associated with symptomatic ischemic stroke recurrence (p < 0.05) in Spanish patients treated with acenocoumarol.
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