Asthma Clinical Trial
Official title:
The Effect of Dietary Supplementation With Encapsulated Fish Oil on Mannitol-induced Airway Sensitivity and Inflammation in Persons With Asthma
We wish to investigate the effects of 3 weeks of orally administered fish oil supplements on the airway sensitivity (provoking dose to cause a 15% fall in FEV1, PD15) to inhaled mannitol (AridolTM). Mannitol, an osmotic stimulus has been demonstrated as a useful model for exercise-induced asthma. We also wish to investigate if there is any associated improvement associated with selected markers of airway inflammation that can be measured in the sputum, blood, urine and exhaled breath condensate. Oral fish oil supplements have recently been demonstrated to be effective inhibitors of exercise-induced asthma, in association with an inhibition of markers of inflammation, over a 3 week treatment period. This finding has important implications in the treatment of asthma as this is a faster and more effective improvement than what is seen with inhaled corticosteroids on exercise-induced asthma. This observation requires validation and further investigation. We wish to study this in two patient groups; (a) steroid naïve asthmatics taking beta2 agonist when required and (b) asthmatics taking regular inhaled corticosteroids < 1000 mcg/day.
Asthma is a chronic inflammatory disorder of the airways characterized by recurrent episodes
of dyspnea, wheeze and chest tightness and is associated with variable airway obstruction.
Exercise-induced bronchoconstriction (EIB) is a feature specific to asthma. Exercise testing
protocols have been developed to identify the presence of asthma as well as to assess asthma
therapy. Airway narrowing following exercise in persons with asthma is thought to result
from dry air hyperpnoea-induced dehydration of the airway surface, leading to the release of
mediators from inflammatory cells residing in the airway. Regular treatment with inhaled
corticosteroids inhibits the airway response to exercise by decreasing the number of
inflammatory cells and thus the source of bronchoconstricting mediators. Therefore, a
decrease in the source of mediator may be the reason for this eventual inhibition of the
airway response to exercise.
It has recently been demonstrated that fish oil supplementation in capsule form, taken daily
over three weeks, provides significant protection against EIB. This protection appears to be
of equal or greater efficacy than inhaled corticosteroids treatment over a similar period.
This may have positive implications in the treatment of asthma as inhaled corticosteroids
are known to have some unwanted side effects. Fish oil supplementation in the high doses
given in previous studies have not demonstrated any side effects and may lead to an
alternative treatment, or a decrease in the dose of inhaled steroids required in the
treatment of asthma.
A new bronchial provocation test using inhaled mannitol, derived from the mechanism of EIB,
has been recently developed and is now registered in Australia and the European Union.
Mannitol causes airway narrowing in a similar manner to exercise in persons with asthma and
is effective in identifying responsiveness to inhaled corticosteroids. We wish to use
inhaled mannitol as a model for EIB in an effort to further investigate the use of fish oil
supplementation in the treatment of asthma. Our hypothesis is that daily orally administered
encapsulated fish oil will attenuate the airway response to mannitol over a 3-week treatment
period. We also wish to measure associated markers of inflammation in the blood, urine,
sputum and exhaled condensate as well as monitor clinical outcomes such as symptoms and
daily beta2 agonist use.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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