A randomized, double-blind trial of the effect of treatment with formoterol on clinical and inflammatory parameters of asthma in children

Ann Allergy Asthma Immunol. 2002 Jul;89(1):67-73. doi: 10.1016/S1081-1206(10)61913-8.

Abstract

Background: In addition to their bronchodilating effect, long-acting inhaled beta-agonists have recently been shown to have some anti-inflammatory properties.

Objective: The purpose of this study was to evaluate the effect of formoterol on inflammatory mediators in children.

Methods: In this double-blind, randomized, placebo-controlled trial, 34 children, aged 6 to 18 years, with moderate atopic asthma, were randomly allocated to receive formoterol or matching placebo for 4 weeks. The primary endpoint of this study was to determine changes in serum levels of inflammatory markers after treatment with formoterol; secondary endpoints included clinical efficacy and bronchial hyperreactivity. The following parameters were measured: symptom score, forced expiratory volume in 1 second (FEV1), provocative concentration of histamine causing a 20% fall in FEV1 (PC20) for histamine and peripheral blood eosinophil count, serum levels of eosinophil cationic protein (ECP), soluble receptor of interleukin-2 (sIL-2R), level of interleukin-4 (IL-4), level of soluble intercellular adhesion molecule-1 (ICAM-1), and immunoglobulin E (IgE) level before and after treatment.

Results: Compared with placebo, treatment with formoterol significantly improved lung function. The mean value of FEV1 changed from 74% of predicted value before treatment to 80% of predicted value after treatment (P < 0.001). The mean concentration of eosinophil blood count before and after treatment was 379 and 310 cells/mm3 (P = 0.035); ECP was 93 and 83 mcg/L; and serum IL-4 was 0.13 and 0.11 pg/mL (P = 0.001). There was no significant difference between formoterol and placebo recipients in PC20H, and serum concentration of sIL-2R, sICAM-1, or IgE after treatment. The group that received formoterol showed improvement in pulmonary function as measured by FEV1 (P < 0.001), and PC20H (P = 0.04) after 4 weeks of treatment. These patients also showed improvement of clinical symptoms (P < 0.001). Serum marker measurements in the formoterol group showed decreased concentrations of eosinophil blood count, ECP, and IL-4, but there was no difference in before and after measurements of sIL-2R, sICAM-1, and IgE.

Conclusions: These results indicate that formoterol has measurable anti-inflammatory properties and can diminish asthma symptoms and bronchial hyperreactivity.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Adrenergic beta-Agonists / therapeutic use*
  • Asthma / drug therapy*
  • Blood Proteins / analysis
  • Bronchodilator Agents / therapeutic use*
  • Child
  • Double-Blind Method
  • Eosinophil Granule Proteins
  • Ethanolamines / therapeutic use*
  • Female
  • Formoterol Fumarate
  • Humans
  • Interleukin-4 / blood
  • Male
  • Receptors, Interleukin-2 / analysis
  • Ribonucleases*

Substances

  • Adrenergic beta-Agonists
  • Blood Proteins
  • Bronchodilator Agents
  • Eosinophil Granule Proteins
  • Ethanolamines
  • Receptors, Interleukin-2
  • Interleukin-4
  • Ribonucleases
  • Formoterol Fumarate