Impact of CYP2D62A, CYP2D64 and CYP3A53 genetic polymorphisms on Bisoprolol peak concentration and clinical response in acute coronary syndrome patients
Aims Acute coronary syndrome (ACS) represents a major cause of death. Bisoprolol is commonly used in the management of ACS. This study aims to investigate the impact of CYP2D6*2A, CYP2D6*4 and CYP3A5*3 genetic polymorphisms on pharmacokinetics and clinical response of bisoprolol in ACS patients. Met...
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Veröffentlicht in: | British journal of clinical pharmacology 2024-10, Vol.90 (10), p.2539-2553 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Aims
Acute coronary syndrome (ACS) represents a major cause of death. Bisoprolol is commonly used in the management of ACS. This study aims to investigate the impact of CYP2D6*2A, CYP2D6*4 and CYP3A5*3 genetic polymorphisms on pharmacokinetics and clinical response of bisoprolol in ACS patients.
Methods
This is an open‐label cohort study that included 127 ACS patients and studied the effect of CYP3A5*3, CYP2D6*2A and CYP2D6*4 genotyping using real‐time polymerase chain reaction on steady state bisoprolol plasma peak concentration analysed by high performance liquid chromatography–fluorescence detector.
Results
Regarding CYP3A5*3, the mean peak bisoprolol concentration for CC, CT and TT genotypes were 4.25 ± 1.20, 3.93 ± 1.10 and 1.79 ± 0.69 ng/mL, respectively (P |
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ISSN: | 0306-5251 1365-2125 1365-2125 |
DOI: | 10.1111/bcp.16134 |