Effect of Montelukast on the Airway Remodeling
Information source: Chinese Academy of Medical Sciences
Information obtained from ClinicalTrials.gov on October 19, 2009 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Asthma
Intervention: leukotriene receptor antagonist (montelukast) (Drug); placebo (Drug)
Phase: Phase 4
Status: Not yet recruiting
Sponsored by: Chinese Academy of Medical Sciences Official(s) and/or principal investigator(s): Jinming Gao, M.D., Ph.D., Principal Investigator, Affiliation: Peking Union Medical College Hospital
Overall contact: Jinming Gao, M.D., Ph.D., Phone: 86-10-6529-5035, Email: gjinming@yahoo.com
Summary
The distal lung contributes to asthmatic airway remodeling which is observed from early
onset of the disease. Cysteinyl leukotrienes (CysLT) play important role in the pathogenesis
of airway remodeling and antileukotrienes work to exert a certain degree of
anti-inflammatory effect. The cysteinyl leukotriene antagonist Montelukast has been in vivo
shown to significantly inhibit ovalbumin induced airway smooth muscle hyperplasia and
subepithelial fibrosis in sensitized mice. This study aims to evaluate if Montelukast could
reverse airway remodeling in asthma patients by a non-invasive approach-HRCT.
Clinical Details
Official title: Effect of Montelukast on the Airway Remodeling in Asthma Patients: Physiological-Radiological Correlation
Study design: Treatment, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Efficacy Study
Primary outcome: Montelukast can improve lung function including proximal and distal airways and reverse airway remodeling in moderate to severe patients with asthma.
Secondary outcome: Montelukast can bring additional benefit for lung function improvement in moderate to severe patients with asthma
Detailed description:
Accumulated data have suggested that the distal lung, which includes airways of < 2mm in
diameter and lung parenchyma, contribute to asthma pathogenesis and symptoms. In addition to
persisting inflammation, distal lung undergoes remodeling, as demonstrated by the reduced
elastic fiber content and abnormal alveolar attachments, with the latter thought to result
in a loss of elastic recoil and a reduction in FEV1. 0. Furthermore, recent studies have
shown that airway remodeling is observed from early onset of the disease and may, therefore,
be characteristic of asthma. Amounting evidence has revealed that airway remodeling of
asthmatic airways accounts for a large component of airway hyperresponsiveness (AHR) and
excessive airway narrowing.
Since remodeling processes occur in parallel to, or may even be obligatory for, the
establishment of persistent inflammation, the pathogenesis of airway remodeling and the
implications of therapeutic interventions that are designed to diminish airway remodeling
remain important areas of both research and clinic. Inhale corticosteroid (ICS) is mainstay
for the treatment of asthma, however, ICS provides very little benefit for airway
remodeling.
Cysteinyl leukotrienes (CysLT) play important role in the pathogenesis of airway remodeling
and antileukotrienes work to exert a certain degree of anti-inflammatory effect. The
cysteinyl leukotriene antagonist Montelukast, for example, has been in vivo shown to
significantly inhibit ovalbumin induced airway smooth muscle hyperplasia and subepithelial
fibrosis in sensitized mice. Montelukast, a systemically delivered leukotriene receptor
antagonist, has been strongly recommended to treat asthma by several guidelines. Clinically,
the systemically acting oral agent montelukast has been shown to improve proximal and distal
lung physiology. In particular, improvements in distal lung function correlate with
improvements in asthma symptoms. The in vivo experiments performed in rodent animal
challenged by OVA have shown that Montelukast can reverse airway remodeling, as well as
inhibit inflammation.
To determine the occurrence of airway remodeling in human being, bronchial biopsy samples
obtained with a bronchoscope are subjected to histological examination. However, bronchial
biopsy is invasive and causes considerable pain, while assessment of the peripheral small
airways and of changes in the deep submucosal tissue and airway smooth muscle in large
airways is technically difficult. This technique does not allow the longitudinal analysis
of airway wall dimensions.
Noninvasive evaluation of airways by means of imaging with high-resolution computed
tomography (HRCT) has therefore been tried as an alternative procedure, and was found to
have the potential to evaluate airways in patients with obstructive pulmonary disease. The
measurement of airway wall thickness by HRCT in patients with asthma has been demonstrated
to correlate with the severity of asthma. Computed tomographic imaging of the airways by
HRCT has been widely applied to investigate the alterations in the structure of the airways
termed airway remodeling in patients with airway obstructive diseases (see references 1-4).
So far to our knowledge, there is no study aiming to evaluate if Montelukast could reverse
airway remodeling in asthma patients by HRCT.
Our encouraging preliminary data performed in 4 patients with moderate to severe asthma
according to GINA definition who received oral Montelukast for 3 months demonstrate with or
without combination of ICS+LABA that there were significant improvements in airway wall
thickness and air trapping evaluated by measurement of HRCT and lung function in patients
with oral Montelukast as compared with those without oral Montelukast. We adopted WA% and
WA/BSA to reflect the degree of airway thickness as published methods. We found that the
patients who received oral montelukast for 3 months experienced improvements in airway
remodeling. WA/BSA and WA% significantly decreased compared to the baseline.
The purpose of the proposal presented is to further examine, in a relatively large number of
patients, that Montelukast can improve the structural changes in the large airways and air
trapping by means of HRCT, and their relationship with pulmonary function in patients in
moderate to severe asthma.
Eligibility
Minimum age: 16 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- forced expiratory volume in one second (FEV1) is at 60-80% predicted or less than
60% predicted
- clinical diagnosis of moderate-to-severe asthma.
Exclusion Criteria:
- intravenous, oral or intramuscular steroids used within 1 months
- Anti-leukotrienes, cromolyn sodium or nedocromil used within 2 months
- Theophylline or beta-adrenergic blockers used within 1 month
- Tobacco Used within the past year or cumulative smoking history > 5 pack-yrs
- Respiratory infection or an influenza vaccination Within 3 weeks
- Pregnant or lactating females
- Patient has a history of an anaphylactic allergic reaction related to administration
of either a marketed or investigational drug
Locations and Contacts
Jinming Gao, M.D., Ph.D., Phone: 86-10-6529-5035, Email: gjinming@yahoo.com
Peking Union Medical College Hospital, Beijing 100730, China
Additional Information
this website provides the updated information on the this study
Related publications: Henderson WR Jr, Chiang GK, Tien YT, Chi EY. Reversal of allergen-induced airway remodeling by CysLT1 receptor blockade. Am J Respir Crit Care Med. 2006 Apr 1;173(7):718-28. Epub 2005 Dec 30. Gono H, Fujimoto K, Kawakami S, Kubo K. Evaluation of airway wall thickness and air trapping by HRCT in asymptomatic asthma. Eur Respir J. 2003 Dec;22(6):965-71. Mitsunobu F, Ashida K, Hosaki Y, Tsugeno H, Okamoto M, Nishida N, Nagata T, Takata S, Tanizaki Y. Decreased computed tomographic lung density during exacerbation of asthma. Eur Respir J. 2003 Jul;22(1):106-12. Zeidler MR, Kleerup EC, Goldin JG, Kim HJ, Truong DA, Simmons MD, Sayre JW, Liu W, Elashoff R, Tashkin DP. Montelukast improves regional air-trapping due to small airways obstruction in asthma. Eur Respir J. 2006 Feb;27(2):307-15. King GG, Müller NL, Paré PD. Evaluation of airways in obstructive pulmonary disease using high-resolution computed tomography. Am J Respir Crit Care Med. 1999 Mar;159(3):992-1004. Review. No abstract available.
Starting date: October 2008
Ending date: April 2011
Last updated: June 16, 2008
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