Literature DB >> 24798717

Future of pharmacogenetics-based therapy for tuberculosis.

Tomoshige Matsumoto1, Masako Ohno, Junichi Azuma.   

Abstract

Personalized medicine uses technology to enable a level of personalization not previously practical. Currently, tuberculosis (TB) therapy is not personalized. Previous reports have shown that a genetic polymorphism of NAT2 is associated with large interindividual and inter-racial differences in the toxicity and efficacy of isoniazid. Herein, we show the safety and efficacy of a pharmacogenetics-based standard TB therapy and also provide a schematic presentation that proposed therapeutic approaches for latent TB infection (LTBI) using NAT2 genotyping. Our data show that the pharmacogenetics-based TB therapy is safer and more efficacious than the standard therapy. Therefore, the therapy using NAT2 genotyping proposed for LTBI herein will be safer and more efficacious than the standard LTBI therapy. Introduction of this therapy with NAT2 genotyping will be one of the cornerstones of personalized medicine.

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Year:  2014        PMID: 24798717     DOI: 10.2217/pgs.14.38

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


  13 in total

1.  Role of the N-acetylation polymorphism in solithromycin metabolism.

Authors:  David W Hein; Mark A Doll
Journal:  Pharmacogenomics       Date:  2017-04-24       Impact factor: 2.533

Review 2.  A microbiological revolution meets an ancient disease: improving the management of tuberculosis with genomics.

Authors:  Marta Wlodarska; James C Johnston; Jennifer L Gardy; Patrick Tang
Journal:  Clin Microbiol Rev       Date:  2015-04       Impact factor: 26.132

Review 3.  Current and future directions in the treatment and prevention of drug-induced liver injury: a systematic review.

Authors:  Jonathan G Stine; James H Lewis
Journal:  Expert Rev Gastroenterol Hepatol       Date:  2015-12-25       Impact factor: 3.869

4.  Predictors of Prolonged TB Treatment in a Dutch Outpatient Setting.

Authors:  Natasha Van't Boveneind-Vrubleuskaya; Alper Daskapan; Jos G W Kosterink; Tjip S van der Werf; Susan van den Hof; Jan-Willem C Alffenaar
Journal:  PLoS One       Date:  2016-11-10       Impact factor: 3.240

5.  Arylamine N-acetyltransferase 2 genotype-dependent N-acetylation of isoniazid in cryopreserved human hepatocytes.

Authors:  Mark A Doll; Raúl A Salazar-González; Srineil Bodduluri; David W Hein
Journal:  Acta Pharm Sin B       Date:  2017-06-07       Impact factor: 11.413

Review 6.  Recommendations for Optimizing Tuberculosis Treatment: Therapeutic Drug Monitoring, Pharmacogenetics, and Nutritional Status Considerations.

Authors:  Rihwa Choi; Byeong Ho Jeong; Won Jung Koh; Soo Youn Lee
Journal:  Ann Lab Med       Date:  2017-03       Impact factor: 3.464

Review 7.  Arylamine N-acetyltransferase acetylation polymorphisms: paradigm for pharmacogenomic-guided therapy- a focused review.

Authors:  David W Hein; Lori M Millner
Journal:  Expert Opin Drug Metab Toxicol       Date:  2020-11-03       Impact factor: 4.481

Review 8.  Drug-Induced Liver Injury: Highlights from a Review of the 2015 Literature.

Authors:  Philip Sarges; Joshua M Steinberg; James H Lewis
Journal:  Drug Saf       Date:  2016-09       Impact factor: 5.228

9.  TLR1 polymorphisms are significantly associated with the occurrence, presentation and drug-adverse reactions of tuberculosis in Western Chinese adults.

Authors:  Wu Peng; Hao Chen; Zhenzhen Zhao; Xuejiao Hu; Yi Zhou; Yingyu Li; Lian Yang; Xuemei Wang; Jiajia Song; Tangyuheng Liu; Qian Wu; Hao Bai; Xiaojun Lu; Jie Chen; Binwu Ying
Journal:  Oncotarget       Date:  2017-12-08

10.  Antituberculosis Drug-Induced Adverse Events in the Liver, Kidneys, and Blood: Clinical Profiles and Pharmacogenetic Predictors.

Authors:  Xuejiao Hu; Mei Zhang; Hao Bai; Lijuan Wu; Yanqing Chen; Liu Ding; Zhenzhen Zhao; Wu Peng; Tangyuheng Liu; Jiajia Song; Yinyu Li; Xiaojun Lu; Xuerong Chen; Yanhong Zhou; Binwu Ying
Journal:  Clin Pharmacol Ther       Date:  2017-11-23       Impact factor: 6.875

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