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HLA-A*24:02 as a common risk factor for antiepileptic drug-induced cutaneous adverse reactions.
Shi, Yi-Wu; Min, Fu-Li; Zhou, Dong; Qin, Bin; Wang, Juan; Hu, Fa-Yun; Cheung, Ying-Kit; Zhou, Jin-Hua; Hu, Xiang-Shu; Zhou, Jue-Qian; Zhou, Lie-Min; Zheng, Zhong-Zheng; Pan, Jie; He, Na; Liu, Zhi-Sheng; Hou, Yun-Qi; Lim, Kheng-Seang; Ou, Yang-Mei; Hui-Ping Khor, Amy; Ng, Ching-Ching; Mao, Bi-Jun; Liu, Xiao-Rong; Li, Bing-Mei; Kuan, Yao-Yun; Yi, Yong-Hong; He, Xue-Lian; Deng, Xiao-Yan; Su, Tao; Kwan, Patrick; Liao, Wei-Ping.
Afiliação
  • Shi YW; Author affiliations are provided at the end of the article.
  • Min FL; Author affiliations are provided at the end of the article.
  • Zhou D; Author affiliations are provided at the end of the article.
  • Qin B; Author affiliations are provided at the end of the article.
  • Wang J; Author affiliations are provided at the end of the article.
  • Hu FY; Author affiliations are provided at the end of the article.
  • Cheung YK; Author affiliations are provided at the end of the article.
  • Zhou JH; Author affiliations are provided at the end of the article.
  • Hu XS; Author affiliations are provided at the end of the article.
  • Zhou JQ; Author affiliations are provided at the end of the article.
  • Zhou LM; Author affiliations are provided at the end of the article.
  • Zheng ZZ; Author affiliations are provided at the end of the article.
  • Pan J; Author affiliations are provided at the end of the article.
  • He N; Author affiliations are provided at the end of the article.
  • Liu ZS; Author affiliations are provided at the end of the article.
  • Hou YQ; Author affiliations are provided at the end of the article.
  • Lim KS; Author affiliations are provided at the end of the article.
  • Ou YM; Author affiliations are provided at the end of the article.
  • Hui-Ping Khor A; Author affiliations are provided at the end of the article.
  • Ng CC; Author affiliations are provided at the end of the article.
  • Mao BJ; Author affiliations are provided at the end of the article.
  • Liu XR; Author affiliations are provided at the end of the article.
  • Li BM; Author affiliations are provided at the end of the article.
  • Kuan YY; Author affiliations are provided at the end of the article.
  • Yi YH; Author affiliations are provided at the end of the article.
  • He XL; Author affiliations are provided at the end of the article.
  • Deng XY; Author affiliations are provided at the end of the article.
  • Su T; Author affiliations are provided at the end of the article.
  • Kwan P; Author affiliations are provided at the end of the article. wpliao@163.net patrick.kwan@unimelb.edu.au.
  • Liao WP; Author affiliations are provided at the end of the article. wpliao@163.net patrick.kwan@unimelb.edu.au.
Neurology ; 88(23): 2183-2191, 2017 Jun 06.
Article em En | MEDLINE | ID: mdl-28476759
ABSTRACT

OBJECTIVE:

To investigate the involvement of human leukocyte antigen (HLA) loci in aromatic antiepileptic drug-induced cutaneous adverse reactions.

METHODS:

A case-control study was performed to detect HLA loci involved in aromatic antiepileptic drug-induced Stevens-Johnson syndrome in a southern Han Chinese population. Between January 1, 2006, and December 31, 2015, 91 cases of Stevens-Johnson syndrome induced by aromatic antiepileptic drugs and 322 matched drug-tolerant controls were enrolled from 8 centers. Important genotypes were replicated in cases with maculopapular eruption and in the meta-analyses of data from other populations. Sequence-based typing determined the HLA-A, HLA-B, HLA-C, and HLA-DRB1 genotypes.

RESULTS:

HLA-B*1502 was confirmed as strongly associated with carbamazepine-induced Stevens-Johnson syndrome (p = 5.63 × 10-15). In addition, HLA-A*2402 was associated significantly with Stevens-Johnson syndrome induced by the aromatic antiepileptic drugs as a group (p = 1.02 × 10-5) and by individual drugs (carbamazepine p = 0.015, lamotrigine p = 0.005, phenytoin p = 0.027). Logistic regression analysis revealed a multiplicative interaction between HLA-B*1502 and HLA-A*2402. Positivity for HLA-A*2402 and/or HLA-B*1502 showed a sensitivity of 72.5% and a specificity of 69.0%. The presence of HLA-A*2402 in cases with maculopapular exanthema was also significantly higher than in controls (p = 0.023). Meta-analysis of data from Japan, Korea, Malaysia, Mexico, Norway, and China revealed a similar association.

CONCLUSIONS:

HLA-A*2402 is a common genetic risk factor for cutaneous adverse reactions induced by aromatic antiepileptic drugs in the southern Han Chinese and possibly other ethnic populations. Pretreatment screening is recommended for people in southern China.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Stevens-Johnson / Predisposição Genética para Doença / Antígeno HLA-A24 / Anticonvulsivantes Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male País como assunto: Asia Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Stevens-Johnson / Predisposição Genética para Doença / Antígeno HLA-A24 / Anticonvulsivantes Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male País como assunto: Asia Idioma: En Ano de publicação: 2017 Tipo de documento: Article