Correlation of thiopurine methyltransferase and inosine triphosphate pyrophosphatase polymorphisms and adverse effects induced by azathioprine treatment in Taiwanese dermatology patients

被引:8
作者
Wang, Ting-Shun [1 ]
Chiu, Hsien-Yi [2 ]
Wu, Lawrence Shih-Hsin [3 ]
Chu, Chia-Yu [1 ]
Tsai, Tsen-Fang [1 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Dermatol, Taipei 100, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Dermatol, Hsin Chu Branch, Hsinchu, Taiwan
[3] Tzu Chi Univ, Inst Med Sci, Hualien, Taiwan
关键词
adverse effects; azathioprine; gene polymorphism; inosine triphosphate pyrophosphatase; thiopurine methyltransferase; INFLAMMATORY-BOWEL-DISEASE; PHENOTYPE-GENOTYPE CORRELATION; BONE-MARROW TOXICITY; S-METHYLTRANSFERASE; DRUG-REACTIONS; CROHNS-DISEASE; PYROPHOSPHOHYDROLASE DEFICIENCY; GENETIC-BASIS; THERAPY; PHARMACOGENETICS;
D O I
10.1016/j.dsi.2013.07.001
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Azathioprine is used as an immunosuppressant and corticosteroid-sparing agent for the treatment of several cutaneous diseases. The mutation of thiopurine methyltransferase (TPMT) and inosine triphosphate pyrophosphatase (ITPA) has been reported to result in the accumulation of toxic thiopurine metabolites and to increase the adverse effects during azathioprine treatment. In the Chinese population, TPMT*3C and ITPA C94A polymorphisms have been documented. Methods: Genotyping was performed for TPMT and ITPA polymorphisms in 92 unrelated healthy volunteers and in 74 dermatology patients (46 with adverse effects and 28 without adverse effects) during azathioprine treatment. Results: Two functional polymorphisms, TPMT*3C and ITPA C94A, were detected. After analysis, ITPA C94A showed weak association with nausea/vomiting induced by azathioprine. Furthermore, we revealed that the ITPA 94 A allele was most common in patients with nausea/vomiting and developing slow-appearing adverse effects (67%), followed by patients with nausea/vomiting but not developing slow-appearing adverse effects (50%) and patients without nausea/vomiting but developing slowappearing adverse effects (25%). Conclusion: Adverse reaction to azathioprine cannot be predicted by TPMT polymorphism. However, genetic testing of ITPA polymorphism may be more important for the prediction of nausea/vomiting in Taiwanese. Currently, regular blood tests and clinical vigilance remain most important in preventing severe drug reactions during clinical use of azathioprine. Copyright (C) 2013, Taiwanese Dermatological Association. Published by Elsevier Taiwan LLC. All rights reserved.
引用
收藏
页码:13 / 18
页数:6
相关论文
共 55 条
[1]   ITPA genotyping test does not improve detection of Crohn's disease patients at risk of azathioprine/6-mercaptopurine induced myelosuppression [J].
Allorge, D ;
Hamdan, R ;
Broly, F ;
Libersa, C ;
Colombel, JF .
GUT, 2005, 54 (04) :565-565
[2]  
[Anonymous], 2006, COMMON TERMINOLOGY C
[3]   Thiopurine methyltransferase activity and the use of azathioprine in inflammatory bowel disease [J].
Ansari, A ;
Hassan, C ;
Duley, J ;
Marinaki, A ;
Shobowale-Bakre, EM ;
Seed, P ;
Meenan, J ;
Yim, A ;
Sanderson, J .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2002, 16 (10) :1743-1750
[4]   Guidelines for prescribing azathioprine in dermatology [J].
Anstey, AV ;
Wakelin, S ;
Reynolds, NJ .
BRITISH JOURNAL OF DERMATOLOGY, 2004, 151 (06) :1123-1132
[5]   Analysis of ITPA phenotype-genotype correlation in the Bulgarian population revealed a novel gene variant in Exon 6 [J].
Atanasova, Srebrena ;
Shipkova, Maria ;
Svinarov, Dobrin ;
Mladenova, Antoaneta ;
Genova, Mariana ;
Wieland, Eberhard ;
Oellerich, Michael ;
von Ahsen, Nicolas .
THERAPEUTIC DRUG MONITORING, 2007, 29 (01) :6-10
[6]   Thiopurine S-methyltransferase genotypic analysis in autoimmune bullous diseases [J].
Bezier, Maud ;
Reguiai, Ziad ;
Vitory, Fabien ;
Broly, Franck ;
Bernard, Philippe .
EUROPEAN JOURNAL OF DERMATOLOGY, 2008, 18 (05) :512-517
[7]   Assessment of Thiopurine S-Methyltransferase Activity in Patients Prescribed Thiopurines: A Systematic Review [J].
Booth, Ronald A. ;
Ansari, Mohammed T. ;
Loit, Evelin ;
Tricco, Andrea C. ;
Weeks, Laura ;
Doucette, Steve ;
Skidmore, Becky ;
Sears, Margaret ;
Sy, Richmond ;
Karsh, Jacob .
ANNALS OF INTERNAL MEDICINE, 2011, 154 (12) :814-823
[8]   Azathioprine-related myelosuppression in a patient homozygous for TPMT☆3A [J].
Budhiraja, Pooja ;
Popovtzer, Mordecai .
NATURE REVIEWS NEPHROLOGY, 2011, 7 (08) :478-484
[9]   Thiopurine Methyltransferase Gene Polymorphisms in Chinese Patients with Inflammatory Bowel Disease [J].
Cao, Qian ;
Zhu, Qin ;
Shang, Yan ;
Gao, Min ;
Si, Jianmin .
DIGESTION, 2009, 79 (01) :58-63
[10]   BSR/BHPR guideline for disease-modifying anti-rheumatic drug (DMARD) therapy in consultation with the British Association of Dermatologists [J].
Chakravarty, K. ;
McDonald, H. ;
Pullar, T. ;
Taggart, A. ;
Chalmers, R. ;
Oliver, S. ;
Mooney, J. ;
Somerville, M. ;
Bosworth, A. ;
Kennedy, T. .
RHEUMATOLOGY, 2008, 47 (06) :924-925