Cutaneous reactions induced by oxcarbazepine in Southern Han Chinese: Incidence, features, risk factors and relation to HLA-B alleles

被引:56
作者
He, Na [1 ,2 ,3 ]
Min, Fu-Li [1 ,2 ,3 ]
Shi, Yi-Wu [1 ,2 ,3 ]
Guo, Jing [1 ,2 ,3 ]
Liu, Xiao-Rong [1 ,2 ,3 ]
Li, Bing-Mei [1 ,2 ,3 ]
Zhou, Jin-Hua [4 ]
Ou, Yang-Mei [4 ]
Liao, Jian-Xiang [5 ]
Liao, Wei-Ping [1 ,2 ,3 ]
机构
[1] Guangzhou Med Univ, Inst Neurosci, Key Lab Neurogenet & Channelopathies Guangdong Pr, Guangzhou 510260, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Affiliated Hosp 2, Key Lab Neurogenet & Channelopathies Guangdong Pr, Guangzhou 510260, Guangdong, Peoples R China
[3] Minist Educ China, Guangzhou 510260, Guangdong, Peoples R China
[4] Guangdong 999 Brain Hosp, Dept Neurol, Guangzhou 510510, Guangdong, Peoples R China
[5] Shenzhen Childrens Hosp, Dept Pediat Neurol, Shenzhen 518026, Peoples R China
来源
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY | 2012年 / 21卷 / 08期
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Oxcarbazepine; Maculopapular eruption; Incidence; Risk factors; HLA-B*1502; STEVENS-JOHNSON-SYNDROME; TOXIC EPIDERMAL NECROLYSIS; SYSTEMIC SYMPTOMS DRESS; ADVERSE DRUG-REACTIONS; ANTIEPILEPTIC DRUGS; HLA-B-ASTERISK-1502; ALLELE; CROSS-REACTIVITY; CLINICAL-TRIAL; DOUBLE-BLIND; SKIN RASHES;
D O I
10.1016/j.seizure.2012.06.014
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Purpose: Oxcarbazepine (OXC) is a promising alternative for patients who cannot tolerate carbamazepine. Recently, however, it has been reported that OXC-induced cutaneous adverse drug reactions (cADRs) are prevalent and may lead to drug discontinuation. Additionally, these reactions are thought to be associated with HLA-B*1502. This study aims to investigate the incidence, features and risk factors of OXC-cADRs, and to explore their relation to HLA-B alleles in Southern Han Chinese. Methods: A prospective study was performed to investigate the incidence, features and risk factors of OXC-cADRs, in which 252 new users were recruited. To examine the association between OXC-cADRs and HLA-B alleles, 14 maculopapular eruption (MPE) cases, including 9 additional cases beyond this prospective observation, were genotyped by PCR-SSP and sequencing. Thirty-five OXC-tolerant patients served as controls. Results: Five patients (2.0%) developed an OXC-cADR, and all were mild MPE. History of other AED allergy (p = 0.005, OR = 121.23) and non-AED allergy (p = 0.006, OR = 59.92) were significant risk factors for OXC-cADRs in multivariate logistic regression analysis. Only one patient with OXC-MPE was positive for HLA-B*1502; and the frequency of HLA-B*1502 in OXC-MPE did not differ significantly from that in OXC-tolerant controls. Four HLA-B*1302 alleles were detected in OXC-MPE cases, which was significantly different from that in general population of southern Han Chinese (p = 0.001, OR = 7.83). Conclusions: The incidence of OXC-induced cADRs was low, and no severe reactions occurred. Patients with a history of allergy are more susceptible to OXC-cADRs. No significant association between HLA-B*1502 and OXC-MPE was found. The associations between OXC-MPE and HLA alleles warrant further studies. (C) 2012 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:614 / 618
页数:5
相关论文
共 36 条
[1]
Cross-reactivity pattern of rash from current aromatic antiepileptic drugs [J].
Alvestad, Sije ;
Lydersen, Stian ;
Brodtkorb, Eylert .
EPILEPSY RESEARCH, 2008, 80 (2-3) :194-200
[2]
Rash from antiepileptic drugs: Influence by gender, age, and learning disability [J].
Alvestad, Silje ;
Lydersen, Stian ;
Brodtkorb, Eylert .
EPILEPSIA, 2007, 48 (07) :1360-1365
[3]
Association study of lamotrigine-induced cutaneous adverse reactions and HLA-B*1502 in a Han Chinese population [J].
An, Dong-Mei ;
Wu, Xin-Tong ;
Hu, Fa-Yun ;
Yan, Bo ;
Stefan, Hermann ;
Zhou, Dong .
EPILEPSY RESEARCH, 2010, 92 (2-3) :226-230
[4]
Comparison and predictors of rash associated with 15 antiepileptic drugs [J].
Arif, H. ;
Buchsbaum, R. ;
Weintraub, D. ;
Koyfman, S. ;
Salas-Humara, C. ;
Bazil, C. W. ;
Resor, S. R., Jr. ;
Hirsch, L. J. .
NEUROLOGY, 2007, 68 (20) :1701-1709
[5]
Oxcarbazepine monotherapy for partial-onset seizures - A multicenter, double-blind, clinical trial [J].
Beydoun, A ;
Sachdeo, RC ;
Rosenfeld, WE ;
Krauss, GL ;
Sessler, N ;
Mesenbrink, P ;
Kramer, L ;
D'Souza, J .
NEUROLOGY, 2000, 54 (12) :2245-2251
[6]
Oxcarbazepine and DRESS syndrome: a paediatric cause of acute liver failure [J].
Bosdure, E ;
Cano, A ;
Roquelaure, B ;
Reynaud, R ;
Boyer, A ;
Viard, L ;
Sarles, J .
ARCHIVES DE PEDIATRIE, 2004, 11 (09) :1073-1077
[7]
Multicentre, double-blind, randomised comparison between lamotrigine and carbamazepine in elderly patients with newly diagnosed epilepsy [J].
Brodie, MJ ;
Overstall, PW ;
Giorgi, L .
EPILEPSY RESEARCH, 1999, 37 (01) :81-87
[8]
Safety profile of oxcarbazepine: Results from a prescription-event monitoring study [J].
Buggy, Yvonne ;
Layton, Deborah ;
Fogg, Carole ;
Shakir, Saad A. W. .
EPILEPSIA, 2010, 51 (05) :818-829
[9]
Oxcarbazepine Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) syndrome mimicking septic shock [J].
Chakarian, Jean-Charles ;
Girault, Christophe ;
Beduneau, Gaetan ;
Duval-Modeste, Anne-Benedicte ;
Joly, Pascal ;
Bonmarchand, Guy .
PRESSE MEDICALE, 2010, 39 (10) :1103-1105
[10]
A marker for Stevens-Johnson syndrome [J].
Chung, WH ;
Hung, SI ;
Hong, HS ;
Hsih, MS ;
Yang, LC ;
Ho, HC ;
Wu, JY ;
Chen, YT .
NATURE, 2004, 428 (6982) :486-486