Beta-1,4-galactosyltransferase 2 c.909C>T gene variant is predictive of on-clopidogrel platelet reactivity

Author:

Pallet Nicolas123,Belleville-Rolland Tiphaine124,Savalle Anne13,Lejeune Manon14,Mauge Laetitia1245,Bertil Sebastien14,Loriot Marie-Anne123,Gaussem Pascale1246

Affiliation:

1. AP-HP, Department of Clinical chemistry, Hôpital Européen Georges Pompidou, Paris, France

2. Paris Descartes University, Sorbonne Paris Cité, Paris, France

3. Institut National pour la Santé et la Recherche Médicale, UMRS 1147, Paris, France

4. AP-HP, Department of Biological Hematology, Hôpital Européen Georges Pompidou, Paris, France

5. Institut National pour la Santé et la Recherche Médicale, UMRS 970, Paris, France

6. Institut National pour la Santé et la Recherche Médicale, UMRS 1140, Paris, France

Abstract

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.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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