PMID- 22727972 OWN - NLM STAT- MEDLINE DCOM- 20140422 LR - 20181202 IS - 1874-1754 (Electronic) IS - 0167-5273 (Linking) VI - 167 IP - 5 DP - 2013 Sep 1 TI - Pantoprazole significantly interferes with antiplatelet effect of clopidogrel: results of a pilot randomized trial. PG - 2177-81 LID - S0167-5273(12)00727-9 [pii] LID - 10.1016/j.ijcard.2012.05.080 [doi] AB - BACKGROUND: The CYP2C19*2 polymorphism is significantly associated with residual platelet reactivity (RPR) and maybe a major confounding factor in studies evaluating pharmacological interactions with clopidogrel. OBJECTIVES: We sought to evaluate the influence of a proton pump inhibitor (PPI), pantoprazole, indicated as relatively less influent than other PPIs, on the antiplatelet effect of clopidogrel, considering a stratification of the population for the presence of cytochrome 2C19*2 polymorphism. METHODS: 105 patients with ST elevation myocardial infarction (STEMI), treated with percutaneous coronary angioplasty (PCI) and who received dual antiplatelet therapy, were randomized between pantoprazole (n=54) or ranitidine (n=51). RPR was evaluated by Platelet Function Analyzer-100 (PFA-100) with collagen-epinephrine (CEPI) and collagene-ADP (CADP) cartridges and by light transmitted aggregometry with 10 muM adenosin diphosphate (ADP) and 1mM arachidonic acid (AA), on 5 (T0) and 30 (T1) days after PCI. RESULTS: Demographic, clinical and procedural data and the prevalence of CYP2C19*2 polymorphism were similar between the two groups. Not statistically differences were observed for CEPI-CT and for the maximal aggregation (MA) values with AA stimulus at both times. We observed a significant increase in MA values with ADP in PPI group at T0 (p=0.01) and T1 (p=0.03). At the multiple regression analysis PPI use remained significantly associated with ADP-MA both at T0 (p=0.05) and T1 (p=0.03). CONCLUSIONS: This is the first documentation in a randomized trial, after correction for the bias of CYP2C19*2 polymorphism, that pantoprazole increases the ADP-MA in patients treated with dual antiplatelet therapy. CI - Copyright (c) 2012 Elsevier Ireland Ltd. All rights reserved. FAU - Parri, Maria Serena AU - Parri MS AD - Fondazione Toscana G Monasterio, Ospedale G. Pasquinucci, Massa, Italy. parri@ifc.cnr.it FAU - Gianetti, Jacopo AU - Gianetti J FAU - Dushpanova, Anar AU - Dushpanova A FAU - Della Pina, Francesca AU - Della Pina F FAU - Saracini, Claudia AU - Saracini C FAU - Marcucci, Rossella AU - Marcucci R FAU - Giusti, Betti AU - Giusti B FAU - Berti, Sergio AU - Berti S LA - eng PT - Journal Article PT - Randomized Controlled Trial DEP - 20120622 PL - Netherlands TA - Int J Cardiol JT - International journal of cardiology JID - 8200291 RN - 0 (2-Pyridinylmethylsulfinylbenzimidazoles) RN - 0 (Platelet Aggregation Inhibitors) RN - 0 (Proton Pump Inhibitors) RN - A74586SNO7 (Clopidogrel) RN - D8TST4O562 (Pantoprazole) RN - OM90ZUW7M1 (Ticlopidine) SB - IM MH - 2-Pyridinylmethylsulfinylbenzimidazoles/administration & dosage/*blood MH - Aged MH - Clopidogrel MH - Drug Interactions/physiology MH - Female MH - Humans MH - Male MH - Middle Aged MH - Myocardial Infarction/*blood/drug therapy/genetics MH - Pantoprazole MH - Pilot Projects MH - Platelet Aggregation Inhibitors/administration & dosage/*blood MH - Platelet Function Tests/methods MH - Prospective Studies MH - Proton Pump Inhibitors/administration & dosage/*blood MH - Ticlopidine/administration & dosage/*analogs & derivatives/blood OTO - NOTNLM OT - CYP2C19*2 OT - Clopidogrel OT - Pantoprazole EDAT- 2012/06/26 06:00 MHDA- 2014/04/23 06:00 CRDT- 2012/06/26 06:00 PHST- 2011/08/10 00:00 [received] PHST- 2012/03/19 00:00 [revised] PHST- 2012/05/27 00:00 [accepted] PHST- 2012/06/26 06:00 [entrez] PHST- 2012/06/26 06:00 [pubmed] PHST- 2014/04/23 06:00 [medline] AID - S0167-5273(12)00727-9 [pii] AID - 10.1016/j.ijcard.2012.05.080 [doi] PST - ppublish SO - Int J Cardiol. 2013 Sep 1;167(5):2177-81. doi: 10.1016/j.ijcard.2012.05.080. Epub 2012 Jun 22.