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
Hauptverfasser: Okda, Sherouk M., El‐Bassiouny, Noha A., El Amrawy, Ahmed Mahmoud, Salahuddin, Ahmad, Elonsy, Sohila M., Kassem, Amira B.
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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 
ISSN:0306-5251
1365-2125
1365-2125
DOI:10.1111/bcp.16134