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DOI 10.1002/cpt.2716

Медицинская библиотека · Clinical pharmacology and therapeutics · 2022

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, Taiwan/Asian Severe Cutaneous Adverse Reaction Consortium

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

Для цитирования: 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, Taiwan/Asian Severe Cutaneous Adverse Reaction Consortium. Implementation of NUDT15 Genotyping to Prevent Azathioprine-Induced Leukopenia for Patients With Autoimmune Disorders in Chinese Population.. Clinical pharmacology and therapeutics. 2022. DOI: 10.1002/cpt.2716.

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