Association of ITPA 94C>A genetic polymorphisms with azathioprine induced adverse effects in the South Indian population
Author:
Deva Reka1ORCID, Rajendran Priyadharsini1, Ramasamy Sivaranjani1, Selvan Senthamizh1, Ramasamy Kesavan1
Affiliation:
1. Pharmacology , JIPMER , Puducherry , India
Abstract
Abstract
Objectives
Azathioprine (AZA) is an effective immunosuppressant commonly used for malignancy and immune-mediated disorders. The association between genetic polymorphisms and AZA-induced adverse effects has not been elucidated. Hence this study aimed to evaluate the relationship between single nucleotide polymorphisms of ITPA (C94A) with azathioprine-induced adverse effects.
Methods
A cross-sectional study was performed on 120 patients who were on AZA therapy for immunobullous disorders and inflammatory bowel disease (IBD). Eligible patients were enrolled from outpatient Departments of dermatology and medical gastroenterology and five mL of blood was collected after obtaining written informed consent. DNA extraction and genotyping were done by phenol–chloroform method and real-time polymerase chain reaction (RT-PCR), respectively.
Results
The minor allele frequency of ITPA (A allele) was 30.8 %. The mutant genotypes of ITPA (C94A) were found to have no significant association with overall adverse effects in the South Indian patients on AZA therapy.
Conclusions
We report no significant association between ITPA rs1127354 genetic polymorphism and adverse effects in the South Indian patients on AZA therapy.
Publisher
Walter de Gruyter GmbH
Subject
Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics
Reference18 articles.
1. Cattaneo, D, Perico, N, Remuzzi, G. From pharmacokinetics to pharmacogenomics: a new approach to tailor immunosuppressive therapy: from pharmacokinetics to pharmacogenomics. Am J Transplant 2004;4:299–310, https://doi.org/10.1111/j.1600-6143.2004.00312.x. 2. Sahasranaman, S, Howard, D, Roy, S. Clinical pharmacology and pharmacogenetics of thiopurines. Eur J Clin Pharmacol 2008;64:753–67, https://doi.org/10.1007/s00228-008-0478-6. 3. Walker, GJ, Harrison, JW, Heap, GA, Voskuil, MD, Andersen, V, Anderson, CA, et al.. Association of genetic variants in NUDT15 with thiopurine-induced myelosuppression in patients with inflammatory bowel disease. JAMA 2019;321:773–85, https://doi.org/10.1001/jama.2019.0709. 4. Jung, YS, Cheon, JH, Hong, SP, Kim, TI, Kim, WH. Clinical outcomes and prognostic factors for thiopurine maintenance therapy in patients with intestinal Behcetʼs disease. Inflamm Bowel Dis 2012;18:750–7, https://doi.org/10.1002/ibd.21757. 5. Khera, S, Trehan, A, Bhatia, P, Singh, M, Bansal, D, Varma, N. Prevalence of TPMT, ITPA and NUDT 15 genetic polymorphisms and their relation to 6MP toxicity in north Indian children with acute lymphoblastic leukemia. Cancer Chemother Pharmacol 2019;83:341–8, https://doi.org/10.1007/s00280-018-3732-3.
|
|