首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Polymorphisms of the CYP2C19 gene in Japanese patients with aspirin-exacerbated respiratory disease.
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Polymorphisms of the CYP2C19 gene in Japanese patients with aspirin-exacerbated respiratory disease.

机译:CYP2C19基因在日本阿司匹林加重呼吸系统疾病患者中的多态性。

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摘要

Aspirin-exacerbated respiratory disease (AERD) is a clinical syndrome characterized by a severe asthma attack after taking aspirin, nonsteroidal anti-inflammatory drugs (NSAIDs), or both. Because aspirin intolerance is found in a specific population, genetic predisposition is considered a crucial determinant for its development. Candidate studies have concentrated on the leukotriene-related genes; however, conflicting results have been reported. Recently, Higashi et al demonstrated that prosta-glandin D_2 was overproduced during aspirin-intolerant broncho-constriction, and no differences in the levels of lipoxygenase products have been found in blood from patients with AERD and those with aspirin-tolerant asthma (ATA).
机译:阿司匹林加重性呼吸道疾病(AERD)是一种临床综合征,其特征在于服用阿司匹林和/或非甾体抗炎药(NSAID)或同时服用这两种药物后会严重发作哮喘。由于在特定人群中发现阿司匹林不耐受,因此遗传易感性被认为是其发展的关键决定因素。候选研究集中在白三烯相关基因上。但是,据报道有矛盾的结果。最近,Higashi等人证明在阿司匹林耐受性支气管收缩期间前列腺素D_2过量产生,在AERD患者和阿司匹林耐受性哮喘(ATA)患者的血液中未发现脂氧合酶产物水平的差异。

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