Antileukotrienes in the treatment of asthma

被引:94
作者
OByrne, PM [1 ]
Israel, E [1 ]
Drazen, JM [1 ]
机构
[1] HARVARD UNIV,SCH MED,BOSTON,MA
关键词
D O I
10.7326/0003-4819-127-6-199709150-00009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: To review the activity in clinical models, the efficacy, and the safety of antileukotrienes as a new class of antiasthma treatment. Data Sources: English-language trials identified from the archival literature, including the MEDLINE database, through 1996; bibliographic references; and textbooks. Study Selection: Reports from placebo-controlled, double-blind, randomized trials were selected. Data Extraction: Study designs and results were extracted from the clinical trial reports. Statistical evaluation of combined results was not attempted. Data Synthesis: The various classes of antileukotrienes have shown activity in clinical models of asthma, including exercise-induced, cold air hyperventilation-induced, allergen-induced, and aspirin-induced bronchoconstriction. In addition, the antileukotrienes partially reverse spontaneous bronchoconstriction in asthmatic persons, an effect additive to that of inhaled beta(2)-agonists. Clinical trials of the antileukotrienes have shown clinical benefit, as measured by reductions in asthma symptom scores, improvements in air flow obstruction, and reductions in the rescue use of inhaled beta(2)-agonists. Some, but not all, of the antileukotrienes have been shown to cause liver microsomal activation with increases in hepatic aminotransferase levels. Conclusions: Antileukotrienes are an important new therapy for asthma. Inhibition of leukotriene synthesis or action has a beneficial effect in the treatment of both induced and spontaneous asthma. These results show that leukotrienes are important mediators of the asthmatic response. In addition, encouraging results have been obtained from clinical trials of antileukotrienes; however, these results do not yet provide guidelines for the optimal clinical use of antileukotrienes in asthma treatment. Such recommendations await the results of further studies.
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页码:472 / 480
页数:9
相关论文
共 109 条
[1]   Prolonged protection against exercise-induced bronchoconstriction by the leukotriene D-4-receptor antagonist cinalukast [J].
Adelroth, E ;
Inman, MD ;
Summers, E ;
Pace, D ;
Modi, M ;
OByrne, PM .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1997, 99 (02) :210-215
[2]   EVALUATION OF PHARMACOTHERAPY FOR EXERCISE-INDUCED ASTHMA [J].
ANDERSON, S ;
SEALE, JP ;
FERRIS, L ;
SCHOEFFEL, R ;
LINDSAY, DA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1979, 64 (06) :612-624
[3]  
ANDERSON SD, 1985, CHEST, V87, P191
[4]   BRONCHIAL RESPONSIVENESS TO INHALED HISTAMINE AND EXERCISE [J].
ANDERTON, RC ;
CUFF, MT ;
FRITH, PA ;
COCKCROFT, DW ;
MORSE, JLC ;
JONES, NL ;
HARGREAVE, FE .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1979, 63 (05) :315-320
[5]  
BALCAREK JM, 1988, J BIOL CHEM, V263, P13937
[6]   CELLULAR EVENTS IN THE BRONCHI IN MILD ASTHMA AND AFTER BRONCHIAL PROVOCATION [J].
BEASLEY, R ;
ROCHE, WR ;
ROBERTS, JA ;
HOLGATE, ST .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 139 (03) :806-817
[7]   THE EFFECT OF AN INHALED LEUKOTRIENE ANTAGONIST, L-648,051, ON EARLY AND LATE ASTHMATIC REACTIONS AND SUBSEQUENT INCREASE IN AIRWAY RESPONSIVENESS IN MAN [J].
BEL, EH ;
TIMMERS, MC ;
DIJKMAN, JH ;
STAHL, EG ;
STERK, PJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1990, 85 (06) :1067-1075
[8]   THE RELEASE OF HISTAMINE AND FORMATION OF A SLOW-REACTING SUBSTANCE (SRS-A) DURING ANAPHYLACTIC SHOCK [J].
BROCKLEHURST, WE .
JOURNAL OF PHYSIOLOGY-LONDON, 1960, 151 (03) :416-435
[9]  
CARTER GW, 1991, J PHARMACOL EXP THER, V256, P929
[10]   ALLERGEN-INDUCED INCREASE IN BRONCHIAL RESPONSIVENESS TO HISTAMINE - RELATIONSHIP TO THE LATE ASTHMATIC RESPONSE AND CHANGE IN AIRWAY CALIBER [J].
CARTIER, A ;
THOMSON, NC ;
FRITH, PA ;
ROBERTS, R ;
HARGREAVE, FE .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1982, 70 (03) :170-177