Treating asthma: is there a place for leukotriene receptor antagonists?

Z Diamant*, T van der Molen

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

12 Citations (Scopus)

Abstract

Asthma is a chronic disorder, characterized by airway hyperresponsiveness (AHR), airway inflammation and airway remodelling. Evidence has been provided for a relationship between pathophysiology, airway inflammation and remodelling. Moreover, these asthma features have been shown to respond to anti-inflammatory therapy. According to current guidelines, monitoring of asthma is predominantly based on symptoms and lung function data. However, these parameters appeared as poor indices for asthma control. Alternatively, asthma control relates well to exacerbations and (anamnestic) surrogate biomarkers of airway inflammation. Hence, appropriate treatment of asthma should primarily target the airway inflammation.

According to current guidelines for asthma management, anti-inflammatory therapy with inhaled corticosteroids (ICS) is the cornerstone in the treatment of persistent asthma. To further optimize asthma control, add-on therapy with long-acting beta(2)-agonists (LABA) or leukotriene receptor antagonists (LTRA) should be combined with low to high doses of ICS. White the first combination focuses on optimal control of symptoms and lung function, the second provides a more complete suppression of the airway inflammation.

In this paper we discuss treatment of asthma according to current guidelines versus new insights, addressing practical issues. (c) 2005 Elsevier Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)655-662
Number of pages8
JournalRespiratory Medicine
Volume99
Issue number6
DOIs
Publication statusPublished - Jun-2005

Keywords

  • leukotriene receptor antagonists
  • airway inflammation
  • asthma
  • RANDOMIZED CONTROLLED-TRIAL
  • DOSE INHALED BUDESONIDE
  • AIRWAY INFLAMMATION
  • PERSISTENT ASTHMA
  • DOUBLE-BLIND
  • MONTELUKAST
  • SALMETEROL
  • EXACERBATIONS
  • HYPERRESPONSIVENESS
  • FLUTICASONE

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