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 in | Frontiers in pharmacology Vol. 13; p. 952804 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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 – name: 1 Department of Cardiology , The First Affiliated Hospital of Nanjing Medical University , Nanjing , Jiangsu , China – name: 4 Lizhu Medical Research Institute , Lizhu Group , Zhuhai , Guangdong , China – name: 6 Department of Clinical Pharmacology , School of Pharmacy College , Nanjing Medical University , Nanjing , China – 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 |
Author_xml | – sequence: 1 givenname: Zekang surname: Ye fullname: Ye, Zekang – sequence: 2 givenname: Pengsheng surname: Chen fullname: Chen, Pengsheng – sequence: 3 givenname: Chuchu surname: Tan fullname: Tan, Chuchu – sequence: 4 givenname: Xiaoxuan surname: Gong fullname: Gong, Xiaoxuan – sequence: 5 givenname: Ran surname: Li fullname: Li, Ran – sequence: 6 givenname: Zhou surname: Dong fullname: Dong, Zhou – sequence: 7 givenname: Inam surname: Ullah fullname: Ullah, Inam – sequence: 8 givenname: Chen surname: Zhou fullname: Zhou, Chen – sequence: 9 givenname: Sufeng surname: Zhou fullname: Zhou, Sufeng – sequence: 10 givenname: Lijun surname: Xie fullname: Xie, Lijun – sequence: 11 givenname: Xuemei surname: Hou fullname: Hou, Xuemei – sequence: 12 givenname: Zhihui surname: Han fullname: Han, Zhihui – sequence: 13 givenname: Qian surname: Gu fullname: Gu, Qian – sequence: 14 givenname: Jiazheng surname: Ma fullname: Ma, Jiazheng – sequence: 15 givenname: Jianzhen surname: Teng fullname: Teng, Jianzhen – sequence: 16 givenname: Yingdan surname: Tang fullname: Tang, Yingdan – sequence: 17 givenname: Zhuanxia surname: Zhang fullname: Zhang, Zhuanxia – sequence: 18 givenname: Haitang surname: Hu fullname: Hu, Haitang – sequence: 19 givenname: Quankun surname: Zhuang fullname: Zhuang, Quankun – sequence: 20 givenname: Juan surname: Chen fullname: Chen, Juan – sequence: 21 givenname: Bei surname: Zhu fullname: Zhu, Bei – sequence: 22 givenname: Feng surname: Shao fullname: Shao, Feng – sequence: 23 givenname: Chunjian surname: Li fullname: Li, Chunjian |
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CitedBy_id | crossref_primary_10_1111_cns_70258 crossref_primary_10_3389_fcvm_2024_1385318 crossref_primary_10_2144_fsoa_2023_0277 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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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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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