Effects of ilaprazole on the steady-state pharmacodynamics of clopidogrel in healthy volunteers: An open-label randomized crossover study

Background: Previous studies have suggested that proton pump inhibitors could impair the antiplatelet effect of clopidogrel. It is uncertain whether ilaprazole affects the antiplatelet effect of clopidogrel. This study aimed to determine the drug-drug interaction between ilaprazole and clopidogrel....

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Published inFrontiers in pharmacology Vol. 13; p. 952804
Main Authors Ye, Zekang, Chen, Pengsheng, Tan, Chuchu, Gong, Xiaoxuan, Li, Ran, Dong, Zhou, Ullah, Inam, Zhou, Chen, Zhou, Sufeng, Xie, Lijun, Hou, Xuemei, Han, Zhihui, Gu, Qian, Ma, Jiazheng, Teng, Jianzhen, Tang, Yingdan, Zhang, Zhuanxia, Hu, Haitang, Zhuang, Quankun, Chen, Juan, Zhu, Bei, Shao, Feng, Li, Chunjian
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LanguageEnglish
Published Frontiers Media S.A 08.09.2022
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Abstract Background: Previous studies have suggested that proton pump inhibitors could impair the antiplatelet effect of clopidogrel. It is uncertain whether ilaprazole affects the antiplatelet effect of clopidogrel. This study aimed to determine the drug-drug interaction between ilaprazole and clopidogrel. Methods: A randomized crossover trial of 40 healthy subjects was performed. Clopidogrel was administered alone or in combination with ilaprazole for 7 days. The maximal platelet aggregation (MPA) to 5 μmol/L adenosine diphosphate was measured by light transmission aggregometry and the platelet reactivity index (PRI) was determined by vasodilator-stimulated phosphoprotein P2Y 12 assay. High on-treatment platelet reactivity (HOPR) was defined as a MPA of >40%. The inhibition of platelet aggregation (IPA) and PRI in the two phases were compared between two regimens after the last dosing. Results: IPA was comparable between the two regimens at 0, 10 and 24 h ( p > 0.05), but higher at 4 h in the clopidogrel alone regimen compared with that in the combined treatment regimen (75.66 ± 18.44% vs. 70.18 ± 17.67%, p = 0.031). The inhibition of PRI was comparable between the two regimens at 0 and 24 h. There were no significant differences in the area under the time-IPA% curve (AUC) or the incidence of HOPR at all time-points between the two regimens. Conclusion: In healthy subjects, ilaprazole has limited effect on the pharmacodynamics of clopidogrel and it may not be clinically relevant. Clinical Trial Registration : [ www.chictr.org.cn ], identifier [ChiCTR2000031482].
AbstractList Background: Previous studies have suggested that proton pump inhibitors could impair the antiplatelet effect of clopidogrel. It is uncertain whether ilaprazole affects the antiplatelet effect of clopidogrel. This study aimed to determine the drug-drug interaction between ilaprazole and clopidogrel. Methods: A randomized crossover trial of 40 healthy subjects was performed. Clopidogrel was administered alone or in combination with ilaprazole for 7 days. The maximal platelet aggregation (MPA) to 5 μmol/L adenosine diphosphate was measured by light transmission aggregometry and the platelet reactivity index (PRI) was determined by vasodilator-stimulated phosphoprotein P2Y12 assay. High on-treatment platelet reactivity (HOPR) was defined as a MPA of >40%. The inhibition of platelet aggregation (IPA) and PRI in the two phases were compared between two regimens after the last dosing. Results: IPA was comparable between the two regimens at 0, 10 and 24 h (p > 0.05), but higher at 4 h in the clopidogrel alone regimen compared with that in the combined treatment regimen (75.66 ± 18.44% vs. 70.18 ± 17.67%, p = 0.031). The inhibition of PRI was comparable between the two regimens at 0 and 24 h. There were no significant differences in the area under the time-IPA% curve (AUC) or the incidence of HOPR at all time-points between the two regimens. Conclusion: In healthy subjects, ilaprazole has limited effect on the pharmacodynamics of clopidogrel and it may not be clinically relevant. Clinical Trial Registration: [www.chictr.org.cn], identifier [ChiCTR2000031482].Background: Previous studies have suggested that proton pump inhibitors could impair the antiplatelet effect of clopidogrel. It is uncertain whether ilaprazole affects the antiplatelet effect of clopidogrel. This study aimed to determine the drug-drug interaction between ilaprazole and clopidogrel. Methods: A randomized crossover trial of 40 healthy subjects was performed. Clopidogrel was administered alone or in combination with ilaprazole for 7 days. The maximal platelet aggregation (MPA) to 5 μmol/L adenosine diphosphate was measured by light transmission aggregometry and the platelet reactivity index (PRI) was determined by vasodilator-stimulated phosphoprotein P2Y12 assay. High on-treatment platelet reactivity (HOPR) was defined as a MPA of >40%. The inhibition of platelet aggregation (IPA) and PRI in the two phases were compared between two regimens after the last dosing. Results: IPA was comparable between the two regimens at 0, 10 and 24 h (p > 0.05), but higher at 4 h in the clopidogrel alone regimen compared with that in the combined treatment regimen (75.66 ± 18.44% vs. 70.18 ± 17.67%, p = 0.031). The inhibition of PRI was comparable between the two regimens at 0 and 24 h. There were no significant differences in the area under the time-IPA% curve (AUC) or the incidence of HOPR at all time-points between the two regimens. Conclusion: In healthy subjects, ilaprazole has limited effect on the pharmacodynamics of clopidogrel and it may not be clinically relevant. Clinical Trial Registration: [www.chictr.org.cn], identifier [ChiCTR2000031482].
Background: Previous studies have suggested that proton pump inhibitors could impair the antiplatelet effect of clopidogrel. It is uncertain whether ilaprazole affects the antiplatelet effect of clopidogrel. This study aimed to determine the drug-drug interaction between ilaprazole and clopidogrel.Methods: A randomized crossover trial of 40 healthy subjects was performed. Clopidogrel was administered alone or in combination with ilaprazole for 7 days. The maximal platelet aggregation (MPA) to 5 μmol/L adenosine diphosphate was measured by light transmission aggregometry and the platelet reactivity index (PRI) was determined by vasodilator-stimulated phosphoprotein P2Y12 assay. High on-treatment platelet reactivity (HOPR) was defined as a MPA of >40%. The inhibition of platelet aggregation (IPA) and PRI in the two phases were compared between two regimens after the last dosing.Results: IPA was comparable between the two regimens at 0, 10 and 24 h (p > 0.05), but higher at 4 h in the clopidogrel alone regimen compared with that in the combined treatment regimen (75.66 ± 18.44% vs. 70.18 ± 17.67%, p = 0.031). The inhibition of PRI was comparable between the two regimens at 0 and 24 h. There were no significant differences in the area under the time-IPA% curve (AUC) or the incidence of HOPR at all time-points between the two regimens.Conclusion: In healthy subjects, ilaprazole has limited effect on the pharmacodynamics of clopidogrel and it may not be clinically relevant.Clinical Trial Registration: [www.chictr.org.cn], identifier [ChiCTR2000031482].
Background: Previous studies have suggested that proton pump inhibitors could impair the antiplatelet effect of clopidogrel. It is uncertain whether ilaprazole affects the antiplatelet effect of clopidogrel. This study aimed to determine the drug-drug interaction between ilaprazole and clopidogrel. Methods: A randomized crossover trial of 40 healthy subjects was performed. Clopidogrel was administered alone or in combination with ilaprazole for 7 days. The maximal platelet aggregation (MPA) to 5 μmol/L adenosine diphosphate was measured by light transmission aggregometry and the platelet reactivity index (PRI) was determined by vasodilator-stimulated phosphoprotein P2Y 12 assay. High on-treatment platelet reactivity (HOPR) was defined as a MPA of >40%. The inhibition of platelet aggregation (IPA) and PRI in the two phases were compared between two regimens after the last dosing. Results: IPA was comparable between the two regimens at 0, 10 and 24 h ( p > 0.05), but higher at 4 h in the clopidogrel alone regimen compared with that in the combined treatment regimen (75.66 ± 18.44% vs. 70.18 ± 17.67%, p = 0.031). The inhibition of PRI was comparable between the two regimens at 0 and 24 h. There were no significant differences in the area under the time-IPA% curve (AUC) or the incidence of HOPR at all time-points between the two regimens. Conclusion: In healthy subjects, ilaprazole has limited effect on the pharmacodynamics of clopidogrel and it may not be clinically relevant. Clinical Trial Registration : [ www.chictr.org.cn ], identifier [ChiCTR2000031482].
Author Chen, Pengsheng
Ma, Jiazheng
Ye, Zekang
Zhou, Chen
Hu, Haitang
Xie, Lijun
Li, Ran
Gu, Qian
Han, Zhihui
Li, Chunjian
Zhang, Zhuanxia
Teng, Jianzhen
Tan, Chuchu
Tang, Yingdan
Shao, Feng
Gong, Xiaoxuan
Zhou, Sufeng
Hou, Xuemei
Dong, Zhou
Ullah, Inam
Zhuang, Quankun
Chen, Juan
Zhu, Bei
AuthorAffiliation 3 Phase I Clinical Trial Unit , The First Affiliated Hospital of Nanjing Medical University , Nanjing , Jiangsu , China
1 Department of Cardiology , The First Affiliated Hospital of Nanjing Medical University , Nanjing , Jiangsu , China
2 Department of Cardiology , Xuzhou Central Hospital , Xuzhou , Jiangsu , China
4 Lizhu Medical Research Institute , Lizhu Group , Zhuhai , Guangdong , China
6 Department of Clinical Pharmacology , School of Pharmacy College , Nanjing Medical University , Nanjing , China
5 Department of Biostatistics , School of Public Health , Nanjing Medical University , Nanjing , Jiangsu , China
AuthorAffiliation_xml – name: 3 Phase I Clinical Trial Unit , The First Affiliated Hospital of Nanjing Medical University , Nanjing , Jiangsu , China
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– name: 2 Department of Cardiology , Xuzhou Central Hospital , Xuzhou , Jiangsu , China
– name: 5 Department of Biostatistics , School of Public Health , Nanjing Medical University , Nanjing , Jiangsu , China
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Copyright Copyright © 2022 Ye, Chen, Tan, Gong, Li, Dong, Ullah, Zhou, Zhou, Xie, Hou, Han, Gu, Ma, Teng, Tang, Zhang, Hu, Zhuang, Chen, Zhu, Shao and Li.
Copyright © 2022 Ye, Chen, Tan, Gong, Li, Dong, Ullah, Zhou, Zhou, Xie, Hou, Han, Gu, Ma, Teng, Tang, Zhang, Hu, Zhuang, Chen, Zhu, Shao and Li. 2022 Ye, Chen, Tan, Gong, Li, Dong, Ullah, Zhou, Zhou, Xie, Hou, Han, Gu, Ma, Teng, Tang, Zhang, Hu, Zhuang, Chen, Zhu, Shao and Li
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Francisco Abad-Santos, Universidad Autónoma de Madrid, Spain
This article was submitted to Drug Metabolism and Transport, a section of the journal Frontiers in Pharmacology
These authors have contributed equally to this work
Reviewed by: Sojeong Yi, United States Food and Drug Administration, United States
Edited by: Stefania Tacconelli, University of Studies G. d’Annunzio Chieti and Pescara, Italy
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Snippet Background: Previous studies have suggested that proton pump inhibitors could impair the antiplatelet effect of clopidogrel. It is uncertain whether ilaprazole...
Background: Previous studies have suggested that proton pump inhibitors could impair the antiplatelet effect of clopidogrel. It is uncertain whether ilaprazole...
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SubjectTerms clopidogrel
drug-drug interaction
ilaprazole
maximal platelet aggregation
Pharmacology
platelet reactivity index
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Title Effects of ilaprazole on the steady-state pharmacodynamics of clopidogrel in healthy volunteers: An open-label randomized crossover study
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https://pubmed.ncbi.nlm.nih.gov/PMC9492925
https://doaj.org/article/6aab7bc56eb14ddabec90096f5edbedd
Volume 13
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