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Year : 2022  |  Volume : 54  |  Issue : 2  |  Page : 97--101

Evaluation of genetic polymorphism of CYP3A5 in normal healthy participants from western India - A cross-sectional study

Miteshkumar Rajaram Maurya, Sunanda Gautam, Jeffrey Pradeep Raj, Shruti Saha, Sanchita Ambre, Aishwarya Thakurdesai, Aditya Shah, Urmila Mukund Thatte 
 Department of Clinical Pharmacology, KEM Hospital, Parel, Mumbai, Maharashtra, India

Correspondence Address:
Dr. Urmila Mukund Thatte
Department of Clinical Pharmacology, Seth GS Medical College and KEM Hospital, Parel, Mumbai - 400 012, Maharashtra
India

BACKGROUND: CYP3A5 enzymes belong to the phase I Group of drug-metabolizing enzymes, which are involved in the metabolism of 50% of the drugs. Participants with CYP3A5 genotype: CYP3A5 *1/*1 are fast metabolizers of drugs and hence will require higher dosing. Whereas those with CYP3A5 * 3/*3 are poor metabolizers of drugs and will require a lower dose to achieve target drug concentration in the blood and those with CYP3A5 * 1/*3 have intermediate drug metabolizing activity. Pharmacogenetic evaluation may improve disease outcomes by maximizing the efficacy and minimizing the toxicity of drugs in patients. MATERIALS AND METHODS: This is a single-center cross-sectional study conducted in the year 2018–2019 to study the population prevalence of genetic polymorphisms of CYP3A5 in healthy participants from western India. Eligible participants willing to give written, informed consent were enrolled in the study. Subsequently, 2 ml venous blood was collected the deoxyribonucleic acid was extracted and then stored at ‒20°C. Genotyping was done by a polymerase chain reaction and restriction fragment length polymorphism. RESULTS: A total of 400 participants with a median age of 22 years (range: 18–58 years) were included. Among them, the genotype prevalence for CYP3A5 * 1/*1 was 17% (n = 67/400); CYP3A5 * 1/*3 was 37% (n = 149/400) and that of CYP3A5 * 3/*3 was 46% (184/400). Out of the total 400 healthy participants analyzed, the allele frequency for CYP3A5 * 1 was 35% (142/400) and that of CYP3A5*3 was 65% (259/400). CONCLUSION: The genotype prevalence for CYP3A5 * 3*3 (46%) and the allele frequency for CYP3A5 * 3 (65%) respectively were the highest among the western Indian population.


How to cite this article:
Maurya MR, Gautam S, Raj JP, Saha S, Ambre S, Thakurdesai A, Shah A, Thatte UM. Evaluation of genetic polymorphism of CYP3A5 in normal healthy participants from western India - A cross-sectional study.Indian J Pharmacol 2022;54:97-101


How to cite this URL:
Maurya MR, Gautam S, Raj JP, Saha S, Ambre S, Thakurdesai A, Shah A, Thatte UM. Evaluation of genetic polymorphism of CYP3A5 in normal healthy participants from western India - A cross-sectional study. Indian J Pharmacol [serial online] 2022 [cited 2022 Jul 3 ];54:97-101
Available from: https://www.ijp-online.com/article.asp?issn=0253-7613;year=2022;volume=54;issue=2;spage=97;epage=101;aulast=Maurya;type=0