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HLA-B*1502 is associated with aromatic anticonvulsant drug-induced cutaneous adverse drug reactions among the Hakka population in China
BACKGROUND: The purpose of this study was to analyze the correlation between aromatic antiepileptic drug-induced cutaneous adverse drug reactions and HLA-B*1502 genotype in patients from the Hakka population in Meizhou. METHODS: A total of 214 epileptic patients taking aromatic (n = 94) or non-aroma...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132569/ https://www.ncbi.nlm.nih.gov/pubmed/32228349 http://dx.doi.org/10.1177/0300060520911276 |
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author | Zheng, Zhiyuan Zhong, Hua Zhang, Qunji Huang, Qingyan Wu, Heming |
author_facet | Zheng, Zhiyuan Zhong, Hua Zhang, Qunji Huang, Qingyan Wu, Heming |
author_sort | Zheng, Zhiyuan |
collection | PubMed |
description | BACKGROUND: The purpose of this study was to analyze the correlation between aromatic antiepileptic drug-induced cutaneous adverse drug reactions and HLA-B*1502 genotype in patients from the Hakka population in Meizhou. METHODS: A total of 214 epileptic patients taking aromatic (n = 94) or non-aromatic anticonvulsants (n = 120) were included in the study from September 2016 to May 2018. Clinical data for the patients were analyzed retrospectively and HLA-B*1502 genotype testing was carried out. RESULTS: Thirty patients were HLA-B*1502(+) (14.02%). The proportion of HLA-B*1502(−) genotype and incidence of adverse drug reactions (ADRs) differed significantly between the two drug groups. In the aromatic anticonvulsant group, maculopapular eruption (MPE), Stevens–Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and hypersensitivity syndrome (HSS) occurred in 10 patients, including eight HLA-B*1502(+) and two HLA-B*1502(−) patients. MPE, HSS, SJS, and TEN occurred in 26 patients in the non-aromatic anticonvulsant group, including one HLA-B*1502(+) and 25 HLA-B*1502(−) patients. There was a significant correlation between the proportions of HLA-B*1502(+) genotype and induced cutaneous adverse drug reactions in the two groups. CONCLUSIONS: HLA-B*1502 is associated with aromatic anticonvulsant drug-induced cutaneous adverse drug reactions among the Hakka population in Meizhou, China. |
format | Online Article Text |
id | pubmed-7132569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-71325692020-04-13 HLA-B*1502 is associated with aromatic anticonvulsant drug-induced cutaneous adverse drug reactions among the Hakka population in China Zheng, Zhiyuan Zhong, Hua Zhang, Qunji Huang, Qingyan Wu, Heming J Int Med Res Retrospective Clinical Research Report BACKGROUND: The purpose of this study was to analyze the correlation between aromatic antiepileptic drug-induced cutaneous adverse drug reactions and HLA-B*1502 genotype in patients from the Hakka population in Meizhou. METHODS: A total of 214 epileptic patients taking aromatic (n = 94) or non-aromatic anticonvulsants (n = 120) were included in the study from September 2016 to May 2018. Clinical data for the patients were analyzed retrospectively and HLA-B*1502 genotype testing was carried out. RESULTS: Thirty patients were HLA-B*1502(+) (14.02%). The proportion of HLA-B*1502(−) genotype and incidence of adverse drug reactions (ADRs) differed significantly between the two drug groups. In the aromatic anticonvulsant group, maculopapular eruption (MPE), Stevens–Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and hypersensitivity syndrome (HSS) occurred in 10 patients, including eight HLA-B*1502(+) and two HLA-B*1502(−) patients. MPE, HSS, SJS, and TEN occurred in 26 patients in the non-aromatic anticonvulsant group, including one HLA-B*1502(+) and 25 HLA-B*1502(−) patients. There was a significant correlation between the proportions of HLA-B*1502(+) genotype and induced cutaneous adverse drug reactions in the two groups. CONCLUSIONS: HLA-B*1502 is associated with aromatic anticonvulsant drug-induced cutaneous adverse drug reactions among the Hakka population in Meizhou, China. SAGE Publications 2020-03-31 /pmc/articles/PMC7132569/ /pubmed/32228349 http://dx.doi.org/10.1177/0300060520911276 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Retrospective Clinical Research Report Zheng, Zhiyuan Zhong, Hua Zhang, Qunji Huang, Qingyan Wu, Heming HLA-B*1502 is associated with aromatic anticonvulsant drug-induced cutaneous adverse drug reactions among the Hakka population in China |
title | HLA-B*1502 is associated with aromatic anticonvulsant drug-induced
cutaneous adverse drug reactions among the Hakka population in
China |
title_full | HLA-B*1502 is associated with aromatic anticonvulsant drug-induced
cutaneous adverse drug reactions among the Hakka population in
China |
title_fullStr | HLA-B*1502 is associated with aromatic anticonvulsant drug-induced
cutaneous adverse drug reactions among the Hakka population in
China |
title_full_unstemmed | HLA-B*1502 is associated with aromatic anticonvulsant drug-induced
cutaneous adverse drug reactions among the Hakka population in
China |
title_short | HLA-B*1502 is associated with aromatic anticonvulsant drug-induced
cutaneous adverse drug reactions among the Hakka population in
China |
title_sort | hla-b*1502 is associated with aromatic anticonvulsant drug-induced
cutaneous adverse drug reactions among the hakka population in
china |
topic | Retrospective Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132569/ https://www.ncbi.nlm.nih.gov/pubmed/32228349 http://dx.doi.org/10.1177/0300060520911276 |
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