نمایش پرونده ساده آیتم

dc.contributor.authorHeidari, R
dc.contributor.authorNiknahad, H
dc.contributor.authorJamshidzadeh, A
dc.contributor.authorAbdoli, N
dc.date.accessioned2018-08-26T08:55:16Z
dc.date.available2018-08-26T08:55:16Z
dc.date.issued2014
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54276
dc.description.abstractMethimazole and propylthiouracil have been used in the management of hyperthyroidism for more than half a century. However, hepatotoxicity is one of the most deleterious side effects associated with these medications. The mechanism(s) of hepatic injury induced by antithyroid agents is not fully recognized yet. Furthermore, there are no specific tools for predicting the occurrence of hepatotoxicity induced by these drugs. The purpose of this article is to give an overview on possible susceptibility factors in liver injury induced by antithyroid agents. Age, gender, metabolism characteristics, alcohol consumption, underlying diseases, immunologic mechanisms, and drug interactions are involved in enhancing antithyroid drugs-induced hepatic damage. An outline on the clinically used treatments for antithyroid drugs-induced hepatotoxicity and the potential therapeutic strategies found to be effective against this complication are also discussed.
dc.language.isoEnglish
dc.relation.ispartofClinical and molecular hepatology
dc.subjectantithyroid agent
dc.subjectprotective agent
dc.subjectreactive oxygen metabolite
dc.subjectanimal
dc.subjectchemistry
dc.subjectdisease model
dc.subjectDrug-Induced Liver Injury
dc.subjectGraves disease
dc.subjecthuman
dc.subjecthyperthyroidism
dc.subjectmetabolism
dc.subjectrisk factor
dc.subjectAnimals
dc.subjectAntithyroid Agents
dc.subjectDisease Models, Animal
dc.subjectDrug-Induced Liver Injury
dc.subjectGraves Disease
dc.subjectHumans
dc.subjectHyperthyroidism
dc.subjectProtective Agents
dc.subjectReactive Oxygen Species
dc.subjectRisk Factors
dc.titleFactors affecting drug-induced liver injury: antithyroid drugs as instances
dc.typeArticle
dc.citation.volume20
dc.citation.issue3
dc.citation.spage237
dc.citation.epage248
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.3350/cmh.2014.20.3.237


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