Nasser S M, Patel M, Bell G S, Lee T H
Department of Allergy and Allied Respiratory Disorders, Guy's Hospital, London, United Kingdom.
Am J Respir Crit Care Med. 1995 May;151(5):1326-30. doi: 10.1164/ajrccm.151.5.7735581.
Patients with aspirin sensitive asthma (ASA) can be desensitized to aspirin but the mechanisms by which this happens are unknown. To test the hypothesis that there may be a reduction in aspirin-induced leukotriene release following aspirin desensitization, we studied nine patients with ASA, 37 +/- 2.3 yr of age (mean +/- SEM) with a baseline FEV1 of 94 +/- 3.5%. Urinary leukotriene E4 (LTE4) and FEV1 were measured before and after ingestion of a threshold dose of aspirin leading to a 15% decrease in FEV1, and then at intervals following desensitization, when a maintenance dose of 600 mg aspirin was ingested. Prior to desensitization, the maximum decrease in FEV1 following ingestion of a threshold dose of aspirin was 15.3 +/- 3.9%, and urinary LTE4 rose from a baseline value of 235 +/- 79.4 pg/mg creatinine to 1,714 +/- 783 pg/mg creatinine at 3 h. Immediately after acute desensitization, which was performed over several days, 600 mg aspirin provoked a maximum decrease in FEV1 of only 3.3 +/- 2.4%, and urinary LTE4 increased from a baseline of 645 +/- 223 pg/mg creatinine to 1,256 +/- 456 pg/mg creatinine. Following ingestion of 600 mg aspirin for 9 +/- 3.2 mo (n = 5; chronic desensitization), urinary LTE4 rose from a basal level of 432 +/- 127 pg/mg creatinine to 749 +/- 257 pg/mg creatinine at 3 h after 600 mg aspirin, and this was accompanied by a maximum decrease in FEV1 of 7.4 +/- 4.5%. Although there was significantly less aspirin-induced LTE4 excretion after acute desensitization, substantial amounts of LTE4 were still produced without any significant change in lung function.(ABSTRACT TRUNCATED AT 250 WORDS)
阿司匹林敏感性哮喘(ASA)患者可对阿司匹林进行脱敏,但脱敏发生的机制尚不清楚。为了验证阿司匹林脱敏后阿司匹林诱导的白三烯释放可能减少这一假说,我们研究了9例ASA患者,年龄37±2.3岁(均值±标准误),基线第一秒用力呼气量(FEV1)为94±3.5%。在摄入导致FEV1下降15%的阈值剂量阿司匹林之前和之后,以及在脱敏后间隔摄入600mg阿司匹林维持剂量时,测量尿白三烯E4(LTE4)和FEV1。在脱敏前,摄入阈值剂量阿司匹林后FEV1的最大下降为15.3±3.9%,尿LTE4在3小时时从基线值235±79.4pg/mg肌酐升至1714±783pg/mg肌酐。在数天内完成急性脱敏后,600mg阿司匹林引起的FEV1最大下降仅为3.3±2.4%,尿LTE4从基线值645±223pg/mg肌酐增至1256±456pg/mg肌酐。在摄入600mg阿司匹林9±3.2个月(n = 5;慢性脱敏)后,600mg阿司匹林摄入3小时时尿LTE4从基础水平432±127pg/mg肌酐升至749±257pg/mg肌酐,同时FEV1最大下降7.4±4.5%。虽然急性脱敏后阿司匹林诱导的LTE4排泄明显减少,但仍产生大量LTE4,且肺功能无明显变化。(摘要截断于250字)