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Research & Reviews: Journal ofPharmaceutical Analysis | ISSN : 2320-0812

Euro Pharma Chemistry & Future Pharma 2019

June 27-28, 2019 | Amsterdam, Netherlands

12th World congress on

Joint Event

4

th

Pharmaceutical Chemistry Conference Future Pharma

Volume 08

Sarvesh Singh et al., Pharmaceutical Analysis 2019, Volume 08

Association of

NAT2

gene polymorphism with anti-tubercular drug

induced hepatotoxicity in North Indian population

Background:

Tuberculosis (TB) is one of the important causes of global mortality

and morbidity. Hepatotoxicity is a most serious adverse drug reaction of anti-TB

drugs. Various genetic factors are associated with drug-induced hepatotoxicity

(DIH). Anti-tubercular drugs are mostly metabolized by N-acetyltransferase

2

(NAT2)

. Therefore, in this study we aim to assess the association between of

NAT2

genotype polymorphism and drug-induced hepatotoxicity (DIH) in North

India population.

Methods:

TB patients were recruited in two groups. Seventy (70) TB patients

were enrolled as tolerant control group who did not develop DIH, whereas 30

TB patients in anti-tubercular DIH group who developed liver injury during

treatment. The genetic polymorphisms of the

NAT2

genes were analyses by PCR-

RFLP. Genotype and allele frequencies were evaluated by t-test and odds ratio

(OR) with 95% confidence intervals (CIs) to evaluate the strength of associations.

Results:

There is high percentage of slow acetylators among North Indian

population.The 4%people were fast acetylators, 34%were intermediate acetylators

and 62% were slow acetylators. Patients with the slow acetylator genotypes were

most common and there was no significant difference between DIH (73.33%) and

non-DIH (61.40%) patients. However, the slow-acetylator genotypes (

NAT2

*6/7,

NAT2

*5/7 and

NAT2

*5/6) were also not significantly different in anti-tubercular

DIH group and tolerant control group.

Conclusion:

In present study,

NAT2

genotype polymorphism was found to have

no association with development of anti- tubercular DIH

Biography

Sarvesh Singh has completed his MBBS from LLRM Medical College, Meerut, India and

MD from King George’s Medical University, Lucknow, India. He is an Associate Professor

in Pharmacology, Department at King George’s Medical University, Lucknow, India. He has

published more than 12 papers in reputed journals.

drsarveshsingh@gmail.com

Sarvesh Singh

King George’s Medical University

India

Co-Author

Divya Yadav, Anil Kumar Saksena,

Rahul Kumar, Preeti Mishra

and

Tanushree Kumar

King George’s Medical University, India