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In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients

Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe drug hypersensitivities with high mortality. Typical over-the-counter drugs of cold medicines are suggested to be causative. As multiple ingredients are generally contained in cold medicines, it is of particular interest...

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Autores principales: Isogai, Hideto, Miyadera, Hiroko, Ueta, Mayumi, Sotozono, Chie, Kinoshita, Shigeru, Tokunaga, Katsushi, Hirayama, Noriaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810500/
https://www.ncbi.nlm.nih.gov/pubmed/24285954
http://dx.doi.org/10.1155/2013/514068
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author Isogai, Hideto
Miyadera, Hiroko
Ueta, Mayumi
Sotozono, Chie
Kinoshita, Shigeru
Tokunaga, Katsushi
Hirayama, Noriaki
author_facet Isogai, Hideto
Miyadera, Hiroko
Ueta, Mayumi
Sotozono, Chie
Kinoshita, Shigeru
Tokunaga, Katsushi
Hirayama, Noriaki
author_sort Isogai, Hideto
collection PubMed
description Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe drug hypersensitivities with high mortality. Typical over-the-counter drugs of cold medicines are suggested to be causative. As multiple ingredients are generally contained in cold medicines, it is of particular interest to investigate which ingredients are responsible for SJS/TEN. However, experimental examination of causal relationships between SJS/TEN and a particular drug molecule is not straightforward. Significant association between HLA-A*02:06 and SJS/TEN with severe ocular surface complications has been observed in the Japanese. In the present study, we have undertaken in silico docking simulations between various ingredients contained in cold medicines available in Japan and the HLA-A*02:06 molecule. We use the composite risk index (CRI) that is the absolute value of the binding affinity multiplied by the daily dose to assess the potential risk of the adverse reactions. The drugs which have been recognized as causative drugs of SJS/TEN in Japan have revealed relatively high CRI, and the association between SJS/TEN and HLA-A*02:06 has been qualitatively verified. The results have also shown that some drugs whose links to SJS/TEN have not been clinically recognized in Japan show the high CRI and suggested that attention should be paid to their adverse drug reactions.
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spelling pubmed-38105002013-11-27 In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients Isogai, Hideto Miyadera, Hiroko Ueta, Mayumi Sotozono, Chie Kinoshita, Shigeru Tokunaga, Katsushi Hirayama, Noriaki J Toxicol Research Article Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe drug hypersensitivities with high mortality. Typical over-the-counter drugs of cold medicines are suggested to be causative. As multiple ingredients are generally contained in cold medicines, it is of particular interest to investigate which ingredients are responsible for SJS/TEN. However, experimental examination of causal relationships between SJS/TEN and a particular drug molecule is not straightforward. Significant association between HLA-A*02:06 and SJS/TEN with severe ocular surface complications has been observed in the Japanese. In the present study, we have undertaken in silico docking simulations between various ingredients contained in cold medicines available in Japan and the HLA-A*02:06 molecule. We use the composite risk index (CRI) that is the absolute value of the binding affinity multiplied by the daily dose to assess the potential risk of the adverse reactions. The drugs which have been recognized as causative drugs of SJS/TEN in Japan have revealed relatively high CRI, and the association between SJS/TEN and HLA-A*02:06 has been qualitatively verified. The results have also shown that some drugs whose links to SJS/TEN have not been clinically recognized in Japan show the high CRI and suggested that attention should be paid to their adverse drug reactions. Hindawi Publishing Corporation 2013 2013-10-12 /pmc/articles/PMC3810500/ /pubmed/24285954 http://dx.doi.org/10.1155/2013/514068 Text en Copyright © 2013 Hideto Isogai et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Isogai, Hideto
Miyadera, Hiroko
Ueta, Mayumi
Sotozono, Chie
Kinoshita, Shigeru
Tokunaga, Katsushi
Hirayama, Noriaki
In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients
title In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients
title_full In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients
title_fullStr In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients
title_full_unstemmed In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients
title_short In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients
title_sort in silico risk assessment of hla-a*02:06-associated stevens-johnson syndrome and toxic epidermal necrolysis caused by cold medicine ingredients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810500/
https://www.ncbi.nlm.nih.gov/pubmed/24285954
http://dx.doi.org/10.1155/2013/514068
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