Author/Authors :
Riaz, Sana Institute of Biomedical and Genetic Engineering, Islamabad, Pakistan , Muhammad Din, Sadia Institute of Biomedical and Genetic Engineering, Islamabad, Pakistan , Usman Tareen, Muhammad Department of Biochemistry - Faculty of Biological Sciences - Quaid-i-Azam University, Islamabad, Pakistan , Tariq, Fizza Department of Biochemistry - Faculty of Biological Sciences - Quaid-i-Azam University, Islamabad, Pakistan , Latif, Yusra Department of Biochemistry - Faculty of Biological Sciences - Quaid-i-Azam University, Islamabad, Pakistan , Siddiqi, Saima Institute of Biomedical and Genetic Engineering, Islamabad, Pakistan , Sultan, Aneesa Department of Biochemistry - Faculty of Biological Sciences - Quaid-i-Azam University, Islamabad, Pakistan , Mansoor, Atika Institute of Biomedical and Genetic Engineering, Islamabad, Pakistan
Abstract :
CYP2C19 polymorphism is associated with pretreatment drug response prediction,
metabolism, and disposition. Pakistan consists of a population comprising of various ethnic
groups residing in different regions of the country each claiming diverse ethnic origins. The
identification of CYP450 genotypic composition of these populations is therefore necessary
to avoid adverse drug reactions in these individuals. The main objective of the study was to
investigate the prevalence of CYP2C19*2 and CYP2C19*17 alleles in these ethnic groups. The
study was conducted on one thousand and twenty-eight (n = 1028) healthy volunteers from nine
ethnic groups of Pakistan namely Brusho (n = 28), Hazara (n = 102), Kalash (n = 64), Pathan
(n = 170), Punjabi (n = 218), Saraiki (n = 59), Brahui (n = 118), Parsi (n = 90), and Sindhi
(n = 179). DNA was extracted from leukocytes and analyzed by allele specific amplification
polymerase chain reaction (ASA-PCR). Multi allelic polymorphism of CYP2C19 led to
four distinct phenotypes identified as extensive metabolizer (EM), poor metabolizer (PM),
intermediate metabolizer (IM), and ultra-rapid metabolizer (UM). Over all, the percentage
of predicted poor metabolizer allele was 29.0% compared to UM allele (23.70%). Among
the studied groups, Saraiki and Brahui showed highest percentage of PM allele (40%, 36%)
whereas Parsi and Hazara had highest percentage of UM allele (37% and 30% respectively).
In conclusion, the high allele frequency of PM (CYP2C19*2 and *17) in Pakistani population
led to the recommendation of a pre-treatment test to monitor drug response and dosage
(personalized medicine) to avoid post-treatment adverse drug reactions.
Keywords :
Ethnic groups , Single nucleotide polymorphisms , Pakistanis , CYP2C19 , Adverse drug reactions , Genotyping