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Effect of corticosteroids on bronchial responsiveness to methacholine in asthmatic children
Insights
Corticosteroids like prednisone significantly reduce bronchial hyperresponsiveness in children with asthma. This improvement in airway sensitivity is linked to baseline lung function before treatment.
Area of Science:
- Pediatric Pulmonology
- Pharmacology
- Respiratory Medicine
Background:
- Asthma is a chronic respiratory disease characterized by bronchial hyperresponsiveness.
- Corticosteroids are a cornerstone therapy for managing asthma.
- The impact of corticosteroids on bronchial reactivity in pediatric asthma requires further elucidation.
Purpose of the Study:
- To investigate the effects of oral prednisone on nonspecific bronchial reactivity in children with asthma.
- To assess changes in methacholine bronchial challenge test (PD20-FEV1) following corticosteroid administration.
Main Methods:
- 10 atopic asthmatic children (9-15 years) underwent methacholine challenges before and after a week of daily oral prednisone (60 mg/day) or placebo.
- Bronchial sensitivity was quantified using the log dose of methacholine causing a 20% fall in FEV1 (PD20-FEV1).
Main Results:
- Prednisone treatment significantly increased PD20-FEV1 in all subjects, indicating reduced bronchial sensitivity (p < 0.001).
- Baseline FEV1 and FEF25-75 improved in patients with initially lower values after prednisone.
- The reduction in bronchial sensitivity was inversely related to the initial degree of airway obstruction (FEV1).
Conclusions:
- A one-week course of high-dose prednisone effectively reduces bronchial hyperresponsiveness in asthmatic children.
- The degree of improvement in airway sensitivity correlates with baseline lung function, suggesting a greater benefit in more obstructed airways.
Abstract:
To elucidate the effects of corticosteroids on nonspecific bronchial reactivity in asthmatic children, inhaled challenges with methacholine were conducted in 10 atopic asthmatic subjects (9 to 15 yr of age) before and after consecutive week-long trials of daily orally administered placebo and prednisone (60 mg/day). Pharmacologic bronchial sensitivity was evaluated as the log dose of methacholine producing a 20% fall in FEV1 (PD20-FEV1). The week-long trial of placebo had no effect on either baseline lung function or PD20-FEV1. On the other hand, after the 1-wk course of prednisone: (1) both baseline FEV1 and FEF25-75 systematically improved in the patients who initially had (i.e., before prednisone) lower values, and (2) PD20-FEV1 significantly increased (p less than 0.001) in all the subjects studied. The magnitude of increase in PD20-FEV1 after prednisone was significantly inversely related (i.e., inverse hyperbola) to the initial degree of airway obstruction (i.e., FEV1) obtained prior to prednisone treatment. Moreover, whereas 6 of 10 patients only minimally changed their baseline FEV1 after prednisone, collectively for all the subjects, the percent increase in PD20-FEV1 after prednisone was directly related (correlation coefficient, 0.70; p less than 0.05) to the corresponding percent increase in baseline FEV1 after prednisone. These findings demonstrate that after a week-long course of high-dose prednisone therapy: (1) a significant reduction occurs in bronchial sensitivity to inhaled methacholine in the asthmatic child, and (2) the degree of diminution in airway sensitivity to methacholine is inversely related to the patient's baseline status of airway obstruction.
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