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Pharmacogenomics ; 22(16): 1041-1056, 2021 11.
Article de Anglais | MEDLINE | ID: mdl-34693729

RÉSUMÉ

Aim: The clinical utility of pharmacogenomics (PGx) has been gaining traction alongside growing evidence that adverse drug reactions (ADRs) have significant genetic associations. Nala PGx Core® is a multi-gene qPCR-based panel of 20 allele variants, comprising 18 SNPs and two CYP2D6 copy number markers across four pharmacogenes - CYP2C9, CYP2C19, CYP2D6 and SLCO1B1. Methods: In this study, we validated the performance of Nala PGx Core® against benchmark methods, on the Singaporean and Indonesian populations. Results & conclusion: Nala PGx Core® demonstrated robust and accurate genotyping when compared with other established benchmarks. Furthermore, the panel successfully characterized alleles of clinical relevance, such as CYP2D6*10 and CYP2D6*36, across major ethnic groups present of Singapore and Indonesia, suggesting its potential for adoption in clinical workflows regionally.


Sujet(s)
Pharmacogénétique/méthodes , Réaction de polymérisation en chaîne/normes , Algorithmes , Asiatiques , Référenciation , Cytochrome P-450 CYP2C19 , Cytochrome P-450 CYP2D6/génétique , Effets secondaires indésirables des médicaments/génétique , Ethnies , Dosage génique , Génotype , Humains , Indonésie , Polymorphisme de nucléotide simple , Reproductibilité des résultats , Singapour
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