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阿司匹林诱发的哮喘:临床特征、发病机制与管理

Aspirin-induced asthma: clinical aspects, pathogenesis and management.

作者信息

Hamad Ahmed M, Sutcliffe Amy M, Knox Alan J

机构信息

Department of Respiratory Medicine, Al-Mansourah University, Al-Dakahlia, Egypt.

出版信息

Drugs. 2004;64(21):2417-32. doi: 10.2165/00003495-200464210-00004.

Abstract

Aspirin (acetylsalicylic acid)-induced asthma (AIA) consists of the clinical triad of asthma, chronic rhinosinusitis with nasal polyps, and precipitation of asthma and rhinitis attacks in response to aspirin and other NSAIDs. The prevalence of the syndrome in the adult asthmatic populations is approximately 4-10%. Respiratory disease in these patients may be aggressive and refractory to treatment. The aetiology of AIA is complex and not fully understood, but most evidence points towards an abnormality of arachidonic acid (AA) metabolism. Cyclo-oxygenase (COX), the rate-limiting enzyme in AA metabolism, exists as two main isoforms. COX-1 is the constitutive enzyme responsible for synthesis of protective prostanoids, whereas COX-2 is induced under inflammatory conditions. A number of theories regarding its pathogenesis have been proposed. The shunting hypothesis proposes that inhibition of COX-1 shunts AA metabolism away from production of protective prostanoids and towards cysteinyl leukotriene (cys-LT) biosynthesis, resulting in bronchoconstriction and increased mucus production. The COX-2 hypothesis proposes that aspirin causes a structural change in COX-2 that results in the generation of products of the lipoxygenase pathway. It is speculated that this may result in the formation of mediators that cause respiratory reactions in AIA. Related studies provide evidence for abnormal regulation of the lipoxygenase pathway, demonstrating elevated levels of cys-LTs in urine, sputum and peripheral blood, before and following aspirin challenge in AIA patients. These studies suggest that cys-LTs are continually and aggressively synthesised before exposure to aspirin and, during aspirin-induced reactions, acceleration of synthesis occurs. A genetic polymorphism of the LTC4S gene has been identified consisting of an A to C transversion 444 nucleotides upstream of the first codon, conferring a relative risk of AIA of 3.89. Furthermore, carriers of the C444 allele demonstrate a dramatic rise in urinary LTE(4) following aspirin provocation, and respond better to the cys-LT antagonist pranlukast than A444 homozygotes.AIA patients have an aggressive form of disease, and treatment should include combination therapy with inhaled corticosteroids, beta(2)-adrenoceptor agonists and LT modifiers. Furthermore, recently developed inhibitors of COX-2 may be safer in patients with AIA.

摘要

阿司匹林(乙酰水杨酸)诱发的哮喘(AIA)由哮喘、伴有鼻息肉的慢性鼻窦炎以及因阿司匹林和其他非甾体抗炎药引发的哮喘和鼻炎发作这一临床三联征组成。该综合征在成年哮喘患者群体中的患病率约为4% - 10%。这些患者的呼吸系统疾病可能较为严重且治疗效果不佳。AIA的病因复杂,尚未完全明确,但大多数证据指向花生四烯酸(AA)代谢异常。环氧化酶(COX)是AA代谢中的限速酶,主要以两种同工型存在。COX - 1是负责合成保护性前列腺素的组成型酶,而COX - 2在炎症条件下被诱导产生。关于其发病机制已提出了多种理论。分流假说认为,COX - 1的抑制使AA代谢从保护性前列腺素的产生转向半胱氨酰白三烯(cys - LT)的生物合成,导致支气管收缩和黏液分泌增加。COX - 2假说认为,阿司匹林会导致COX - 2发生结构变化,从而产生脂氧合酶途径的产物。据推测,这可能导致形成在AIA中引发呼吸反应的介质。相关研究为脂氧合酶途径的异常调节提供了证据,表明在AIA患者接受阿司匹林激发前后,尿液、痰液和外周血中的cys - LT水平升高。这些研究表明,在接触阿司匹林之前,cys - LT就持续且大量合成,并且在阿司匹林诱发的反应期间,合成加速。已鉴定出LTC4S基因的一种基因多态性,其在第一个密码子上游444个核苷酸处发生A到C的转换,赋予AIA的相对风险为3.89。此外,C444等位基因的携带者在阿司匹林激发后尿LTE(4)显著升高,并且比A444纯合子对cys - LT拮抗剂普仑司特的反应更好。AIA患者的病情较为严重,治疗应包括吸入性糖皮质激素、β(2) - 肾上腺素能受体激动剂和白三烯调节剂的联合治疗。此外,最近开发的COX - 2抑制剂对AIA患者可能更安全。

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