Sestini P, Refini R M, Pieroni M G, Vaghi A, Robuschi M, Bianco S
Institute of Respiratory Diseases, University of Siena, Italy.
J Allergy Clin Immunol. 1997 Jul;100(1):71-7. doi: 10.1016/s0091-6749(97)70197-0.
Conflicting results have been reported on the effect of non-steroidal antiinflammatory drugs on allergen-induced asthmatic responses. The aim of this study was to investigate the effect of inhaled lysine acetylsalicylate (LASA) on the early and late allergen-induced responses. We studied 16 patients with mild, stable asthma who had an early asthmatic response and 10 patients with a dual (early and late) response. Each patient underwent two challenges with a single dose of allergen assessed in a preliminary test, after inhalation of either 720 mg of LASA in 4 ml of saline solution or placebo, according to a randomized, double-blind protocol. Allergen-induced hyperreactivity to methacholine was measured in six patients from each of the early and the dual response groups 2 hours and 24 hours after the challenge, respectively. In the patients with early response, the maximum fall in FEV1 after challenge was 24% +/- 1% after inhalation of placebo and 14% +/- 2% after inhalation of LASA (p < 0.005). No protection was observed in four patients who received the drug orally instead of by inhalation. In the patients with a dual response, the maximum FEV1 decrease during the early response was 27% +/- 2% after placebo and 21% +/- 2% after LASA (p < 0.025). During the late response (between 3 and 8 hours), the maximum decrease in FEV1 was 28% +/- 4% after placebo and 16% +/- 4% after LASA (p < 0.005). In both groups allergen challenge caused a significant reduction in methacholine PD20 after treatment with placebo but not with LASA. Without allergen challenge, LASA had no effect on methacoline reactivity. We conclude that inhaled LASA significantly reduces both the early and the late asthmatic response to allergen challenge and that it prevents the allergen-induced airway hyperresponsiveness that follows these responses.
关于非甾体抗炎药对变应原诱导的哮喘反应的影响,已有相互矛盾的研究结果报道。本研究旨在探讨吸入赖氨酸乙酰水杨酸酯(LASA)对变应原诱导的早期和晚期反应的影响。我们研究了16例有早期哮喘反应的轻度、稳定哮喘患者和10例有双重(早期和晚期)反应的患者。根据随机、双盲方案,每位患者在初步试验中用单剂量变应原进行两次激发试验,分别吸入4ml盐溶液中720mg的LASA或安慰剂。在激发试验后2小时和24小时,分别对早期反应组和双重反应组的6例患者测定变应原诱导的对乙酰甲胆碱的高反应性。在有早期反应的患者中,激发试验后吸入安慰剂后FEV1的最大下降为24%±1%,吸入LASA后为14%±2%(p<0.005)。4例口服而非吸入该药物的患者未观察到保护作用。在有双重反应的患者中,早期反应期间FEV1的最大下降在吸入安慰剂后为27%±2%,吸入LASA后为21%±2%(p<0.025)。在晚期反应期间(3至8小时),FEV1的最大下降在吸入安慰剂后为28%±4%,吸入LASA后为16%±4%(p<0.005)。在两组中,变应原激发试验在使用安慰剂治疗后导致乙酰甲胆碱PD20显著降低,但使用LASA后未降低。在没有变应原激发试验的情况下,LASA对乙酰甲胆碱反应性没有影响。我们得出结论,吸入LASA可显著降低对变应原激发试验的早期和晚期哮喘反应,并可预防这些反应后出现的变应原诱导的气道高反应性。