Asthma Clinical Trial
Official title:
The Effect of Theophylline in Patients With Allergic Rhinitis
Allergic rhinitis and asthma are common respiratory diseases, which often coexist. The prevalence of allergic rhinitis in subjects with asthma is up to 80%, and the prevalence of asthma is 3-5 times greater in subjects with rhinitis than healthy controls. The mechanisms of the allergen response in both diseases are parallel to each other, with similar mediator and cellular responses to similar allergens. These observations have led to the suggestion that both diseases are different expressions of one airway disease.We wish to evaluate the effect of low dose theophylline in patients with asthma, given its effects as subtherapeutic concentrations and the propensity to develop adverse events at higher doses.
The disease modifying treatments for asthma and rhinitis mirror each other. The first line
therapy being the topical corticosteroids, for which there is good evidence of superiority
over other therapies. They work by altering the transcription of genes involved in the
inflammatory process, thereby favourably influencing the synthesis of inflammatory proteins
and cytokines. They have been shown to reduce the numbers of inflammatory cells and their
inflammatory action. Other disease modifying therapies such as anti-IgE antibodies improve
allergic symptoms in both asthma and rhinitis. Theophylline has been used for many years as
a treatment for asthma but has not been used to help patients with rhinitis.
Theophylline has been considered a weak bronchodilator for many years. However relatively
recently, it was shown to have anti-inflammatory effects in patients with asthma. It reduces
eosinophil counts and eosinophilic cationic protein (ECP) concentration in induced sputum of
asthmatic patients. The combination of low dose theophylline has greater effects on lung
function and asthma severity than high dose inhaled corticosteroids.
Aubier el al have shown, using a nasal allergen challenge model of rhinitis, that 3 weeks
treatment with slow release oral theophylline reduced the increase in the concentration of
eosinophilic cationic protein (ECP) and the percentage of eosinophils in nasal lavage
following the challenge. Furthermore there was a significant reduction in nasal symptoms in
those patients treated with theophylline. However theophylline has not previously been
evaluated as a therapeutic option in patients with chronic rhinitis in the clinic setting.
Cigarette smoking is a major cause of morbidity in patients with asthma and has been shown
to be independently associated with impaired quality of life in asthmatic children. Recent
evidence suggests that patients with asthma who smoke are relatively resistant to inhaled or
oral corticosteroid therapy, with larger doses being required for clinical benefit. The
actual mechanism for this observation is unknown however one hypothesis is that smoking has
an effect on histone deacetylase. It is known that theophylline can active histone
deacetylase and therefore improve the efficacy of corticosteroids.
Theophylline causes significant adverse effects at high doses. Unfortunately the
bronchodilator effect occurs at doses very close to those causing adverse effects. This low
therapeutic index for bronchodilation means that therapeutic monitoring is required. However
the anti-inflammatory effect of theophylline and the effect of theophylline on histone
deacetylase activity occurs at concentrations lower therapeutic level for bronchodilation.
Why have we chosen a dose of 200mg twice daily? In the study by Evans et al which compared
low dose inhaled budesonide plus theophylline to high dose inhaled budesonide, greater
effects with the theophylline combination were seen in terms of pulmonary function and
hyperresponsiveness at serum concentrations of theophylline that were sub therapeutic
(8.7mg/ml). Anti-inflammatory effects are seen in patients with chronic obstructive
pulmonary disease at theophylline concentrations that are subtherapeutic. There have been
studies in patients with asthma that have shown anti-inflammatory effects at in patients
with asthma at doses of 250mg twice daily and 200mg twice daily. We wish therefore to
evaluate the effect of low dose theophylline in patients with asthma, given its effects as
subtherapeutic concentrations and the propensity to develop adverse events at higher doses.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
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