首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Aspirin-induced asthma: advances in pathogenesis, diagnosis, and management.
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Aspirin-induced asthma: advances in pathogenesis, diagnosis, and management.

机译:阿司匹林诱发的哮喘:发病机理,诊断和治疗的进展。

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摘要

In some asthmatic individuals, aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) that inhibit cyclooxygen-ase 1 (COX-1) exacerbate the condition. This distinct clinical syndrome, called aspirin-induced asthma (AIA), is characterized by an eosinophilic rhinosinusitis, nasal polyposis, aspirin sensitivity, and asthma. There is no in vitro test for the disorder, and diagnosis can be established only by provocation challenges with aspirin or NSAIDs. Recent major advances in the molecular biology of eicosanoids, exemplified by the cloning of 2 cysteinyl leukotriene receptors and the discovery of a whole family of cyclooxygenase enzymes, offer new insights into mechanisms operating in AIA. The disease runs a protracted course even if COX-1 inhibitors are avoided, and the course is often severe, many patients requiring systemic corticosteroids to control their sinusitis and asthma. Aspirin and NSAIDs should be avoided, but highly specific COX-2 inhibitors, known as coxibs, are well tolerated andcan be safely used. Aspirin desensitization, followed by daily aspirin treatment, is a valuable therapeutic option in most patients with AIA, particularly those with recurrent nasal polyposis or overdependence on systemic corticosteroids.
机译:在一些哮喘患者中,阿司匹林和其他抑制环氧化酶1(COX-1)的非甾体抗炎药(NSAIDs)使病情恶化。这种独特的临床综合征称为阿司匹林诱发性哮喘(AIA),其特征是嗜酸性鼻窦炎,鼻息肉,阿司匹林敏感性和哮喘。目前尚无对该疾病的体外测试,只有通过使用阿司匹林或NSAID激发性攻击才能确定诊断。类花生酸类分子生物学的最新进展,例如2个半胱氨酰白三烯受体的克隆以及整个环氧合酶家族的发现,为在友邦保险中发挥作用的机制提供了新见解。即使避免使用COX-1抑制剂,该病的病程也很漫长,病程通常很严重,许多患者需要全身性糖皮质激素来控制鼻窦炎和哮喘。应避免使用阿司匹林和非甾体抗炎药,但高度耐受的COX-2抑制剂(称为coxibs)耐受性良好,可以安全使用。在大多数AIA患者中,特别是那些复发性鼻息肉病或过度依赖全身性皮质类固醇的患者,阿司匹林脱敏和每日阿司匹林治疗是一种有价值的治疗选择。

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