使用白三烯调节剂治疗哮喘的最新进展。

James P Kemp
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引用次数: 53

摘要

哮喘是一种慢性呼吸道炎症性疾病,全世界约有1亿人受其影响。为了减轻症状,改善肺功能,降低发病率,目前的治疗指南强调控制哮喘患者潜在炎症的重要性。白三烯是白细胞产生的脂质介质,可促进气道炎症。认识到白三烯在哮喘发病机制中的重要性,导致了白三烯修饰剂的开发,这是25年来治疗哮喘的第一类新药物。目前使用的四种白三烯调节剂(美国的孟鲁司特、zafirlukast和zileuton以及日本的pranlukast)的对照临床试验已经证实了它们在改善肺功能、减轻症状、减少夜间觉醒和减少对急救药物的需求方面的疗效。它们发挥抗炎作用,减轻细胞浸润和支气管高反应性,补充吸入皮质类固醇的抗炎特性。在中度和重度哮喘患者中,它们允许逐渐减少皮质类固醇剂量。在运动性哮喘患者中,白三烯调节剂限制了肺功能的下降并加速了肺功能的恢复,而没有慢性长效β(2)-肾上腺素能受体激动剂的耐受性问题。在阿司匹林(乙酰水杨酸)诱发的哮喘患者中,它们能改善肺功能,并使剂量反应曲线向右移动,减少患者对阿司匹林的反应。对于伴有或不伴有哮喘的季节性变应性鼻炎患者,它们可改善鼻、眼和咽喉症状以及生活质量。白三烯修饰剂通常是安全且耐受性良好的,其副作用与安慰剂相似。白三烯调节剂引起的一个安全性问题,Churg-Strauss综合征,似乎是揭示了一种已经存在的综合征,当白三烯调节剂允许减少皮质类固醇剂量时,这种综合征就会显现出来。虽然目前的治疗指南建议将其用于轻度持续性哮喘患者,但这些指南是在白三烯调节剂进入市场时制定的,在许多临床疗效数据发表之前。由于哮喘是一种异质性疾病,不同的哮喘表型对治疗的反应不同;因此,哮喘治疗需要个体化。白三烯调节剂增加了哮喘患者的治疗选择,根据最近的数据,预计未来的指南将描述这些药物在这些药物有效的临床情况下的扩大用途。
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Recent advances in the management of asthma using leukotriene modifiers.

Asthma is a chronic inflammatory disease of the airways that affects approximately 100 million people worldwide. In order to reduce symptoms, improve pulmonary function, and decrease morbidity, current treatment guidelines emphasize the importance of controlling the underlying inflammation in patients with asthma. Leukotrienes are leukocyte-generated lipid mediators that promote airway inflammation. Recognition of the importance of leukotrienes in the pathogenesis of asthma has led to the development of leukotriene modifiers, the first new class of drugs for the treatment of asthma to become available in 25 years. Controlled clinical trials with the four currently used leukotriene modifiers (montelukast, zafirlukast, and zileuton in the US and pranlukast in Japan) have established their efficacy in improving pulmonary function, reducing symptoms, decreasing night-time awakenings, and decreasing the need for rescue medications. They exert anti-inflammatory effects that attenuate cellular infiltration and bronchial hyperresponsiveness and complement the anti-inflammatory properties of inhaled corticosteroids. In patients with moderate and severe asthma, they permit tapering of the corticosteroid dose. In patients with exercise-induced asthma, leukotriene modifiers limit the decline in and quicken the recovery of pulmonary functions without the tolerance issues seen with chronic long-acting beta(2)-adrenoceptor agonist use. In patients with aspirin (acetylsalicylic acid)-induced asthma, they improve pulmonary function and shift the dose response curve to the right, reducing the patient's response to aspirin. In patients with seasonal allergic rhinitis, with or without concomitant asthma, they improve nasal, eye, and throat symptoms as well as quality of life. Leukotriene modifiers are generally safe and well tolerated with adverse effect profiles similar to that of placebo. The one safety issue raised with leukotriene modifiers, Churg-Strauss Syndrome, appears to be the unmasking of an already present syndrome that is manifested when the leukotriene modifiers permit corticosteroid doses to be reduced. Although current treatment guidelines recommend their use in patients with mild persistent asthma, these guidelines were developed just as leukotriene modifiers were coming to the market, before much of the clinical efficacy data were published. Because asthma is a heterogeneous disease, the different asthma phenotypes respond differently to therapies; consequently asthma therapy needs to be individualized. Leukotriene modifiers increase the therapeutic options for patients with asthma and, based on recent data, it is expected that future guidelines will describe expanded uses for these agents in clinical circumstances where these drugs are effective.

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