Benefits from adding the 5-lipoxygenase inhibitor zileuton to conventional therapy in aspirin-intolerant asthmatics

被引:275
作者
Dahlén, B [1 ]
Nizankowska, E
Szczeklik, A
Zetterström, O
Bochenek, G
Kumlin, M
Mastalerz, L
Pinis, G
Swanson, LJ
Boodhoo, TI
Wright, S
Dubé, LM
Dahlén, SE
机构
[1] Karolinska Inst, Karolinska Hosp, Dept Med, Div Resp Med, SE-17176 Stockholm, Sweden
[2] Karolinska Inst, Natl Inst Environm Med, Stockholm, Sweden
[3] Jagiellonian Univ, Dept Med, Sch Med, Cracow, Poland
[4] Abbott Labs, Immunosci Venture, Chicago, IL USA
关键词
D O I
10.1164/ajrccm.157.4.9707089
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
From bronchoprovocation studies and investigations of the acute effects of drugs that inhibit leukotrienes (LT), the hypothesis has emerged that leukotrienes are important mediators of airway obstruction and other symptoms in aspirin-intolerant asthma (AIA). However, it has yet not been shown if subjects with AIA respond favorably to clinical treatment with leukotriene inhibitors. Therefore, in a double-blind placebo-controlled crossover study, we examined the effects of 6 wk of treatment with the leukotriene-pathway inhibitor zileuton (600 mg, four times daily) in 40 patients with well-characterized AIA. The treatment was added to existing therapy, which included medium to high doses of inhaled (average daily dose 1,030 mu g of beclomethasone or budesonide) or oral glucocorticosteroids (4 to 25 mg/d) for all but one of the patients. On top of this treated baseline, there were no significant effects of adding placebo, indicating that their asthma was kept relatively stable. However, there was an acute and chronic improvement in pulmonary function after treatment with zileuton, expressed both as increased FEV1 from baseline compared with placebo, and higher morning and evening peak expiratory flow rate (PEFR) values on zileuton treatment compared with placebo. The improvements occurred despite lower use of rescue bronchodilator with zileuton. Zileuton also diminished nasal dysfunction, which is one of the cardinal signs of AIA. There was a remarkable return of smell, less rhinorrhea, and a trend for less stuffiness and higher nasal inspiratory flow during treatment with zileuton. Zileuton caused a small but distinct reduction of bronchial hyperresponsiveness to histamine and inhibited aspirin-induced bronchoconstriction. Zileuton inhibited urinary excretion of LTE4 but did not change airway reactivity to inhaled LTD4, supporting that zileuton specifically inhibited leukotriene biosynthesis. The findings indicate that leukotrienes are important mediators of persistent airway obstruction and chronic nasal dysfunction in AIA. The study also suggests that addition of a leukotriene pathway inhibitor such as zileuton may bring about greater control of asthma than what is achieved by treatment with medium to high doses of glucocorticosteroids alone.
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页码:1187 / 1194
页数:8
相关论文
共 35 条
[1]   AIRWAY RESPONSIVENESS TO HISTAMINE AND LEUKOTRIENE-E4 IN SUBJECTS WITH ASPIRIN-INDUCED ASTHMA [J].
ARM, JP ;
OHICKEY, SP ;
SPUR, BW ;
LEE, TH .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 140 (01) :148-153
[2]   EFFECT OF LEUKOTRIENE D4 ON NASAL MUCOSAL BLOOD-FLOW, NASAL AIRWAY-RESISTANCE AND NASAL SECRETION IN HUMANS [J].
BISGAARD, H ;
OLSSON, P ;
BENDE, M .
CLINICAL ALLERGY, 1986, 16 (04) :289-297
[3]   URINARY LEUKOTRIENE-E4 CONCENTRATIONS INCREASE AFTER ASPIRIN CHALLENGE IN ASPIRIN-SENSITIVE ASTHMATIC SUBJECTS [J].
CHRISTIE, PE ;
TAGARI, P ;
FORDHUTCHINSON, AW ;
CHARLESSON, S ;
CHEE, P ;
ARM, JP ;
LEE, TH .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1991, 143 (05) :1025-1029
[4]   THE POTENT AND SELECTIVE SULFIDOPEPTIDE LEUKOTRIENE ANTAGONIST, SK-AND-F-104353, INHIBITS ASPIRIN-INDUCED ASTHMA [J].
CHRISTIE, PE ;
SMITH, CM ;
LEE, TH .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1991, 144 (04) :957-958
[5]  
DAHLEN B, 1993, EUR RESPIR J, V6, P1018
[6]   EFFECT OF THE LEUKOTRIENE RECEPTOR ANTAGONIST MK-0679 ON BASE-LINE PULMONARY-FUNCTION IN ASPIRIN-SENSITIVE ASTHMATIC SUBJECTS [J].
DAHLEN, B ;
MARGOLSKEE, DJ ;
ZETTERSTROM, O ;
DAHLEN, SE .
THORAX, 1993, 48 (12) :1205-1210
[7]   The effect of inhaled leukotriene D-4 and methacholine on sputum cell differentials in asthma [J].
Diamant, Z ;
Hiltermann, JT ;
vanRensen, EL ;
Callenbach, PM ;
VeselicCharvat, M ;
vanderVeen, H ;
Sont, JK ;
Sterk, PJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 155 (04) :1247-1253
[8]   EFFECT OF ORAL PREDNISONE ON AIRWAY INFLAMMATORY MEDIATORS IN ATOPIC ASTHMA [J].
DWORSKI, R ;
FITZGERALD, GA ;
OATES, JA ;
SHELLER, JR ;
WORKMAN, R ;
PRAKASH, C .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 149 (04) :953-959
[9]   DIRECT EVIDENCE FOR A ROLE OF THE MAST-CELL IN THE NASAL RESPONSE TO ASPIRIN IN ASPIRIN-SENSITIVE ASTHMA [J].
FISCHER, AR ;
ROSENBERG, MA ;
LILLY, CM ;
CALLERY, JC ;
RUBIN, P ;
COHN, J ;
WHITE, MV ;
IGARASHI, Y ;
KALINER, MA ;
DRAZEN, JM ;
ISRAEL, E .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1994, 94 (06) :1046-1056
[10]   ADDED SALMETEROL VERSUS HIGHER-DOSE CORTICOSTEROID IN ASTHMA PATIENTS WITH SYMPTOMS ON EXISTING INHALED CORTICOSTEROID [J].
GREENING, AP ;
IND, PW ;
NORTHFIELD, M ;
SHAW, G .
LANCET, 1994, 344 (8917) :219-224