Key result
The B4GALT2 c.909C>T variant was identified as a potential independent genetic predictor of on-treatment platelet reactivity in 174 patients under dual antiplatelet therapy.
Why the study?
Does the B4GALT2 c.909C>T gene variant predict on-treatment platelet reactivity in patients on clopidogrel-based dual antiplatelet therapy?
Observational (n=174)
Does the B4GALT2 c.909C>T gene variant predict on-treatment platelet reactivity in patients on clopidogrel-based dual antiplatelet therapy?
The B4GALT2 c.909C>T variant may serve as an independent genetic predictor of clopidogrel sensitivity and on-treatment platelet reactivity.
CYP2C19 genotype influences clopidogrel response but only accounts for a small part of the variability in platelet reactivity. Recently, exome sequencing identified a variant of the gene encoding B4GALT2 as a potential candidate implicated in on-treatment platelet reactivity. Carriers of the B4GALT2 c.909C>T variant have lower platelet reactivity indicating that B4GALT2 could influence clopidogrel sensitivity and could expose to the risk of bleeding events. We undertook this observational retrospective study to determine if B4GALT2 c.909C>T influences P2RY12-specific vasodilator-stimulated phosphoprotein phosphorylation and agonist-induced platelet aggregation in a nonselected cohort of 174 patients under clopidogrel-based antiplatelet therapy. Our results indicate that in individuals under dual antiplatelet therapy, B4GALT2 c.909C>T might be an independent genetic predictor of on-treatment platelet reactivity.
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Pallet et al. (2018) conducted an observational in Patients under clopidogrel-based antiplatelet therapy (n=174). B4GALT2 c.909C>T variant was evaluated on P2RY12-specific vasodilator-stimulated phosphoprotein phosphorylation and agonist-induced platelet aggregation. The B4GALT2 c.909C>T variant was identified as a potential independent genetic predictor of on-treatment platelet reactivity in 174 patients under dual antiplatelet therapy.
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