García-Marcos Luis, Schuster Antje, Pérez-Yarza Eduardo G
Department of Pediatrics, University of Murcia and Pediatric Research Unit, Cartagena, Spain.
Drug Saf. 2003;26(7):483-518. doi: 10.2165/00002018-200326070-00004.
Antileukotrienes are a relatively new class of anti-asthma drugs that either block leukotriene synthesis (5-lipoxygenase inhibitors) like zileuton, or antagonise the most relevant of their receptors (the cysteinyl leukotriene 1 receptor [CysLT1]) like montelukast, zafirlukast or pranlukast. Hence, their major effect is an anti-inflammatory one. With the exception of pranlukast, the other antileukotrienes have been studied and marketed in the US and Europe for long enough to establish that they are useful drugs in the management of asthma. Their effects, significantly better than placebo, seem more pronounced in subjective measurements (i.e. symptoms scores or quality-of-life tests) than in objective parameters (i.e. forced expiratory volume in 1 second or peak expiratory flow rate). Also, there is some evidence that these drugs work better in some subsets of patients with certain genetic polymorphisms - probably related to their leukotriene metabolism - or patients with certain asthma characteristics. There are a small number of comparative studies only, and with regard to long-term asthma control differences between the agents have not been evaluated. Nevertheless, their overall effect appears comparable with sodium cromoglycate (cromolyn sodium) or theophylline, but significantly less than low-dose inhaled corticosteroids. Antileukotrienes have been shown to have a degree of corticosteroid-sparing effect, but salmeterol appears to perform better as an add-on drug. Montelukast is probably the most useful antileukotriene for continuous treatment of exercise-induced asthma, performing as well as salmeterol without inducing any tolerance. All antileukotrienes are taken orally; their frequency of administration is quite different ranging from four times daily (zileuton) to once daily (montelukast). Antileukotrienes are well tolerated drugs, even though zileuton intake has been related to transitional liver enzyme elevations in some cases. Also Churg-Strauss syndrome (a systemic vasculitis), has been described in small numbers of patients taking CysLT1 antagonists. It is quite probable that this disease appears as a consequence of an 'unmasking' effect when corticosteroid dosages are reduced in patients with severe asthma once CysLT1 antagonists are introduced, but more data are needed to definitely establish the mechanism behind this effect. Overall, however, the benefits of antileukotrienes in the treatment of asthma greatly outweigh their risks.
抗白三烯药物是一类相对较新的抗哮喘药物,它们要么像齐留通那样阻断白三烯合成(5-脂氧合酶抑制剂),要么像孟鲁司特、扎鲁司特或普仑司特那样拮抗其最相关的受体(半胱氨酰白三烯1受体 [CysLT1])。因此,它们的主要作用是抗炎。除普仑司特外,其他抗白三烯药物在美国和欧洲已进行了足够长时间的研究和销售,足以证明它们是治疗哮喘的有效药物。它们的效果明显优于安慰剂,在主观测量(即症状评分或生活质量测试)中似乎比在客观参数(即一秒用力呼气量或呼气峰值流速)中更显著。此外,有一些证据表明,这些药物在某些具有特定基因多态性的患者亚组中效果更好——可能与他们的白三烯代谢有关——或者在某些具有特定哮喘特征的患者中效果更好。仅有少量比较研究,且尚未评估这些药物在长期哮喘控制方面的差异。然而,它们的总体效果似乎与色甘酸钠(色甘酸二钠)或茶碱相当,但明显低于低剂量吸入性糖皮质激素。已证明抗白三烯药物具有一定程度的糖皮质激素节省作用,但沙美特罗作为附加药物似乎表现更好。孟鲁司特可能是连续治疗运动诱发性哮喘最有用的抗白三烯药物,其效果与沙美特罗相当,且不会产生任何耐受性。所有抗白三烯药物均口服给药;它们的给药频率差异很大,从每日四次(齐留通)到每日一次(孟鲁司特)。抗白三烯药物耐受性良好,尽管在某些情况下服用齐留通与转氨酶短暂升高有关。此外,在少数服用CysLT1拮抗剂的患者中也出现了Churg-Strauss综合征(一种系统性血管炎)。很可能这种疾病是在重度哮喘患者引入CysLT1拮抗剂后,当糖皮质激素剂量减少时由于“暴露”效应而出现的,但需要更多数据来明确确定这种效应背后的机制。然而,总体而言,抗白三烯药物在治疗哮喘方面的益处远大于其风险。