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PLOS ONE  2014 

Increased Risk for Developing Major Adverse Cardiovascular Events in Stented Chinese Patients Treated with Dual Antiplatelet Therapy after Concomitant Use of the Proton Pump Inhibitor

DOI: 10.1371/journal.pone.0084985

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Abstract:

Background Some clinical studies have demonstrated that the proton pump inhibitor (PPI) could decrease clopidogrel platelet response and increase major adverse cardiovascular events (MACE) in white or black subjects. However, that remains to be determined in Chinese patients. In this study, we sought to determine whether there could be an increased risk for developing MACE after concomitant use of dual antiplatelet therapy (DAT) and a PPI in Chinese patients treated with percutaneous coronary intervention (PCI) and stenting. Methods This study was a 5-year, single-center, retrospective cohort analysis of eligible patients (n = 6188) who received DAT and a PPI concomitantly (defined as PPI users) before discharge and/or 12-month follow-up after discharge as compared with those who received DAT alone (also defined as non-PPI users, n = 1465). The incidence of recurrent MACE, such as myocardial infarction (MI), definite stent thromboses (ST), or cardiovascular death, was compared between the PPI users and non-users. Results PPI users had a significantly higher incidence of the MACE than non-users (13.9% vs. 10.6%; adjusted HR: 1.33; 95% CI: 1.12 – 1.57, P = 0.007). Stratified analysis revealed that concurrent use of DAT and a PPI was associated with a significantly increased risk for developing ST compared with DAT alone (1% vs. 0.4%; adjusted HR: 2.66, 95% CI: 1.16 – 5.87, P = 0.012). However, there were no significant differences in the risk of MI, cardiovascular death and other adverse events, regardless of combination of clopidogrel and a PPI. Conclusions The study further suggests that concomitant use of DAT and a PPI may be associated with an increased risk for developing MACE, in particular definite ST, in Chinese PCI patients after discharge as compared with use of DAT alone.

References

[1]  Anderson JL, Adams CD, Antman EM, Bridges CR, Califf RM, et al. (2011) 2011 ACCF/AHA focused update incorporated into the ACC/AHA 2007 guidelines for the management of patients with unstable angina/non-ST-elevation myocardial infarction, a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation 123: e426–579.
[2]  Savi P, Zachayus JL, Delesque-Touchard N, Labouret C, Herve C, et al. (2006) The active metabolite of clopidogrel disrupts P2Y12 receptor oligomers and partitions them out of lipid rafts. Proc Natl Acad Sci USA 103: 11069–11074.
[3]  Kim KA, Park PW, Hong SJ, Park JY (2008) The effect of CYP2C19 polymorphism on the pharmacokinetics and pharmacodynamics of clopidogrel, a possible mechanism for clopidogrel resistance. Clin Pharmacol Ther 84: 236–242.
[4]  Simon T, Verstuyft C, Mary-Krause M, Quteineh L, Drouet E, et al. (2009) Genetic determinants of response to clopidogrel and cardiovascular events. N Engl J Med 360: 363–375.
[5]  Mega JL, Close SL, Wiviott SD, Shen L, Hockett RD, et al. (2009) Cytochrome p-450 polymorphisms and response to clopidogrel. N Engl J Med 360: 354–362.
[6]  Bhatt DL, Scheiman J, Abraham NS, Antman EM, Chan FK, et al. (2008) ACCF / ACG/ AHA 2008 expert consensus document on reducing the gastrointestinal risks of antiplatelet therapy and NSAID use, a report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents. J Am Coll Cardiol 52: 1502–1517.
[7]  Pham CQ, Regal RE, Bostwick TR, Knauf KS (2006) Acid suppressive therapy use on an inpatient internal medicine service. Ann Pharmacother 40: 1261–1266.
[8]  Li XQ, Andersson TB, Ahlstrom M, Weidolf L (2004) Comparison of inhibitory effects of the proton pump-inhibiting drugs omeprazole, esomeprazole, lansoprazole, pantoprazole, and rabeprazole on human cytochrome P450 activities. Drug Metab Dispos 32: 821–827.
[9]  Lim PW, Goh KL, Wong BC (2005) CYP2C19 genotype and the PPIs–focus on rabeprazole. J Gastroenterol Hepatol 20 (suppl): s22–28.
[10]  Small DS, Farid NA, Payne CD, Weerakkody GJ, Li YG, et al. (2008) Effects of the proton pump inhibitor lansoprazole on the pharmacokinetics and pharmacodynamics of prasugrel and clopidogrel. J Clin Pharmacol 48: 475–484.
[11]  Ferreiro JL, Ueno M, Capodanno D, Desai B, Dharmashankar K, et al. (2010) Pharmacodynamic effects of concomitant versus staggered clopidogrel and omeprazole intake, results of a prospective randomized crossover study. Circ Cardiovasc Interv 3: 436–441.
[12]  Angiolillo DJ, Gibson CM, Cheng S, Ollier C, Nicolas O, et al. (2011) Differential effects of omeprazole and pantoprazole on the pharmacodynamics and pharmacokinetics of clopidogrel in healthy subjects, randomized, placebo-controlled, crossover comparison studies. Clin Pharmacol Ther 89: 65–74.
[13]  Ho PM, Maddox TM, Wang L, Fihn SD, Jesse RL, et al. (2009) Risk of adverse outcomes associated with concomitant use of clopidogrel and proton pump inhibitors following acute coronary syndrome. JAMA 301: 937–944.
[14]  Huang CC, Chen YC, Leu HB, Chen TJ, Lin SL, et al. (2010) Risk of adverse outcomes in Taiwan associated with concomitant use of clopidogrel and proton pump inhibitors in patients who received percutaneous coronary intervention. Am J Cardiol 105: 1705–1709.
[15]  Stockl KM, Le L, Zakharyan A, Harada AS, Solow BK, et al. (2010) Risk of rehospitalization for patients using clopidogrel with a proton pump inhibitor. Arch Intern Med 170: 704–710.
[16]  Charlot M, Ahlehoff O, Norgaard ML, Jorgensen CH, Sorensen R, et al. (2010) Proton-pump inhibitors are associated with increased cardiovascular risk independent of clopidogrel use. Ann Intern Med 153: 378–386.
[17]  O’Donoghue ML, Braunwald E, Antman EM, Murphy SA, Bates ER, et al. (2009) Pharmacodynamic effect and clinical efficacy of clopidogrel and prasugrel with or without a proton-pump inhibitor, an analysis of two randomised trials. Lancet 374: 989–997.
[18]  Ray WA, Murray KT, Griffin MR, Chung CP, Smalley WE, et al. (2010) Outcomes with concurrent use of clopidogrel and proton-pump inhibitors. Ann Intern Med 152: 337–345.
[19]  Rassen JA, Choudhry NK, Avorn J, Schneeweiss S (2009) Cardiovascular outcomes and mortality in patients using clopidogrel with proton pump inhibitors after percutaneous coronary intervention or acute coronary syndrome. Circulation 120: 2322–2329.
[20]  Xie HG, Zou JJ, Hu ZY, Zhang JJ, Ye F, et al. (2011) Individual variability in the disposition of and response to clopidogrel: Pharmacogenomics and beyond. Pharmacol Ther 129: 267–289.
[21]  Xie HG, Kim RB, Wood AJJ, Stein CM (2001) Molecular basis of ethnic differences in drug metabolism and response. Annu Rev Pharmacol Toxicol 41: 815–850.
[22]  Mauri L, Hsieh WH, Massaro JM, Ho KK, D’Agostino R, et al. (2007) Stent thrombosis in randomized clinical trials of drug-eluting stents. N Engl J Med 356: 1020–1029.
[23]  Chen SL, Santoso T, Zhang JJ, Ye F, Xu YW, et al. (2011) A Randomized Clinical Study Comparing Double Kissing Crush With Provisional Stenting for Treatment of Coronary Bifurcation Lesions. J Am Coll Cardiol 57: 914–920.
[24]  Cutlip DE, Windecker S, Mehran R, Boam A, Cohen DJ, et al. (2007) Clinical end points in coronary stent trials, a case for standardized definitions. Circulation 115: 2344–2351.
[25]  Gilard M, Arnaud B, Cornily JC, Le Gal G, Lacut K, et al. (2008) Influence of omeprazole on the antiplatelet action of clopidogrel associated with aspirin, the randomized, double-blind OCLA (omeprazole clopidogrel aspirin) study. J Am Coll Cardiol 51: 256–260.
[26]  Siller-Matula JM, Spiel AO, Lang IM, Kreiner G, Christ G, et al. (2009) Effects of pantoprazole and esomeprazole on platelet inhibition by clopidogrel. Am Heart J 157: e1–5.
[27]  Zuern CS, Geisler T, Lutilsky N, Winter S, Schwab M, et al. (2010) Effect of comedication with proton pump inhibitors (PPIs) on post-interventional residual platelet aggregation in patients undergoing coronary stenting treated by dual antiplatelet therapy. Thromb Res 125: e51–54.
[28]  Furuta T, Iwaki T, Umemura K (2010) Influences of different proton pump inhibitors on the antiplatelet function of clopidogrel in relation to CYP2c19 genotypes. Br J Clin Pharmacol 70: 383–392.
[29]  Bhatt DL, Cryer BL, Contant CF, Cohen M, Lanas A, et al. (2010) Clopidogrel with or without omeprazole in coronary artery disease. N Engl J Med 363: 1909–1917.
[30]  Pezalla E, Day D, Pulliadath I (2008) Initial assessment of a drug interaction between clopidogrel and proton pump inhibitors. J Am Coll Cardiol 52: 1038–1039.

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