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锂盐和β受体阻滞剂诱发及加重银屑病的机制。

The mechanism of lithium and beta-blocking agents in inducing and exacerbating psoriasis.

作者信息

O'Brien Meghan, Koo John

机构信息

University of Massachusetts Medical School, Worcester, MA, USA.

出版信息

J Drugs Dermatol. 2006 May;5(5):426-32.

Abstract

Documentation of psoriatic eruptions occurring with the initiation of various pharmacotherapy agents has been reported in the literature. Two such agents include lithium and beta-blocking drugs. By understanding the mechanism by which these drugs induce and exacerbate psoriasis, we may gain further understanding of the disease process of psoriasis as well as how to treat this side effect. This paper reviews the literature that has examined the mechanism by which lithium and beta-blockers may induce and exacerbate psoriasis. Mechanisms involving both immunologic and non-immunologic factors have been examined in various studies. No consensus has been reached and further investigation is needed. However, findings such as improvement with inositol supplementation in cases of lithium-induced and -exacerbated psoriasis and disparate histologic presentation of beta-blocker-induced psoriasis provide suggestions that both the origin and treatment of drug-induced psoriasis may be different than psoriasis that is unrelated to medications.

摘要

文献中已报道了在开始使用各种药物治疗剂时出现银屑病皮疹的情况。其中两种药物是锂盐和β受体阻滞剂。通过了解这些药物诱发和加重银屑病的机制,我们可以进一步了解银屑病的疾病过程以及如何治疗这种副作用。本文回顾了研究锂盐和β受体阻滞剂可能诱发和加重银屑病机制的文献。各种研究中已探讨了涉及免疫和非免疫因素的机制。目前尚未达成共识,需要进一步研究。然而,如锂盐诱发和加重的银屑病病例中补充肌醇后病情改善,以及β受体阻滞剂诱发的银屑病有不同的组织学表现等研究结果表明,药物性银屑病的起源和治疗可能与非药物性银屑病不同。

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