Your browser doesn't support javascript.
loading
Implementation of NUDT15 Genotyping to Prevent Azathioprine-Induced Leukopenia for Patients With Autoimmune Disorders in Chinese Population.
Wang, Chuang-Wei; Chi, Min-Hui; Tsai, Tsen-Fang; Yu, Kuang-Hui; Kao, Hsiao-Wen; Chen, Hsiang-Cheng; Chen, Chun-Bing; Lu, Chun-Wei; Chen, Wei-Ti; Chang, Ya-Ching; Chang, Chih-Jung; Chang, Yun-Ting; Jan Wu, Yeong-Jian; Chang, Chee-Jen; Huang, Yu Huei; Ng, Chau-Yee; Huang, Po-Wei; Lin, Yu-Jr; Hui, Rosaline Chung-Yee; Chung, Wen-Hung.
Afiliação
  • Wang CW; Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Linkou, Taipei and Keelung, Taiwan.
  • Chi MH; Cancer Vaccine and Immune Cell Therapy Core Laboratory, Chang Gung Memorial Hospital, Linkou, Taiwan.
  • Tsai TF; Chang Gung Immunology Consortium, Chang Gung Memorial Hospital Chang Gung University, Taoyuan, Taiwan.
  • Yu KH; Department of Dermatology, Xiamen Chang Gung Hospital, Xiamen, China.
  • Kao HW; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Chen HC; Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Linkou, Taipei and Keelung, Taiwan.
  • Chen CB; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Lu CW; Institute of Molecular Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Chen WT; Department of Dermatology, National Taiwan University Hospital, Taipei, Taiwan.
  • Chang YC; Department of Dermatology, National Taiwan University College of Medicine, Taipei, Taiwan.
  • Chang CJ; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Chang YT; Division of Rheumatology, Department of Internal Medicine, Chang Gung Memorial Hospital, Linkou, Taiwan.
  • Jan Wu YJ; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Chang CJ; Division of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, Linkou, Taiwan.
  • Huang YH; Division of Rheumatology, Immunology and Allergy, Department of Medicine, Tri-Service General Hospital, Taipei, Taiwan.
  • Ng CY; Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Linkou, Taipei and Keelung, Taiwan.
  • Huang PW; Chang Gung Immunology Consortium, Chang Gung Memorial Hospital Chang Gung University, Taoyuan, Taiwan.
  • Lin YJ; Department of Dermatology, Xiamen Chang Gung Hospital, Xiamen, China.
  • Hui RC; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Chung WH; Whole-Genome Research Core Laboratory of Human Diseases, Chang Gung Memorial Hospital, Keelung, Taiwan.
Clin Pharmacol Ther ; 112(5): 1079-1087, 2022 11.
Article em En | MEDLINE | ID: mdl-35869597
Azathioprine (AZA) is commonly used for many autoimmune disorders; however, the limitation of its clinical use is due to potential toxicities, including severe leukopenia. Recent studies have identified genetic NUDT15 variants strongly associated with AZA-induced leukopenia in Asian patients. This study aimed to investigate the strength of above genetic association and evaluate the usefulness of prospective screening of the NUDT15 variants to prevent AZA-induced leukopenia in Chinese patients. AZA-induced leukopenia in patients with autoimmune disorders were enrolled from multiple medical centers in Taiwan/China between 2012 and 2017 to determine the strength of genetic association of NUDT15 or TPMT variants by whole exome sequencing (WES). Furthermore, a prospective study was conducted between 2018 and 2021 to investigate the incidence of AZA-induced leukopenia with and without genetic screening. The WES result showed the genetic variants of NUDT15 R139C (rs116855232) (P = 3.7 × 10-25 , odds ratio (OR) = 21.7, 95% confidence interval (95% CI) = 12.1-38.8) and NUDT15 rs746071566 (P = 4.2 × 10-9 , OR = 7.1, 95% CI = 3.7-13.7), but not TPMT, were associated with AZA-induced leukopenia and NUDT15 R139C variant shows the highest sensitivity with 92.5%. Furthermore, the targeted screening of 1,013 participants for NUDT15 R139C enabled those identified as carriers to use alternative immunosuppressants. This strategy resulted in a significant decrease in the incidence of AZA-induced leukopenia compared with historical incidence (incidence rate = from 7.6% decreased to 0.4%; P = 9.3 × 10-20 ). In conclusion, the NUDT15 R139C variant was strongly associated with AZA-induced leukopenia in Chinese patients. The genetic screening of NUDT15 R139C followed by use of alternative immunosuppressants in identified carriers effectively decreased the incidence of AZA leukopenia for patients with autoimmune disorders.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article