TY - JOUR
T1 - Characterization of within-subject responses to fluticasone and montelukast in childhood asthma
AU - Szefler, Stanley J.
AU - Phillips, Brenda R.
AU - Martinez, Fernando D.
AU - Chinchilli, Vernon M.
AU - Lemanske, Robert F.
AU - Strunk, Robert C.
AU - Zeiger, Robert S.
AU - Larsen, Gary
AU - Spahn, Joseph D.
AU - Bacharier, Leonard B.
AU - Bloomberg, Gordon R.
AU - Guilbert, Theresa W.
AU - Heldt, Gregory
AU - Morgan, Wayne J.
AU - Moss, Mark H.
AU - Sorkness, Christine A.
AU - Taussig, Lynn M.
N1 - Funding Information:
Supported by grants 5U10HL064287, 5U10HL064288, 5U10HL064295, 5U10HL064307, 5U10HL064305, and 5U10HL064313 from the National Heart, Lung, and Blood Institute. This study was carried out in part in the General Clinical Research Centers at Washington University School of Medicine (M01 RR00036) and National Jewish Medical and Research Center (M01 RR00051).
PY - 2005/2
Y1 - 2005/2
N2 - Background: Responses to inhaled corticosteroids (ICSs) and leukotriene receptor antagonists (LTRAs) vary among asthmatic patients. Objective: We sought to determine whether responses to ICSs and LTRAs are concordant for individuals or whether asthmatic patients who do not respond to one medication respond to the other. Methods: Children 6 to 17 years of age with mild-to-moderate persistent asthma were randomized to one of 2 crossover sequences, including 8 weeks of an ICS, fluticasone propionate (100 μg twice daily), and 8 weeks of an LTRA, montelukast (5-10 mg nightly depending on age), in a multicenter, double-masked, 18-week trial. Response was assessed on the basis of improvement in FEV1 and assessed for relationships to baseline asthma phenotype-associated biomarkers. Results: Defining response as improvement in FEV1 of 7.5% or greater, 17% of 126 participants responded to both medications, 23% responded to fluticasone alone, 5% responded to montelukast alone, and 55% responded to neither medication. Compared with those who responded to neither medication, favorable response to fluticasone alone was associated with higher levels of exhaled nitric oxide, total eosinophil counts, levels of serum IgE, and levels of serum eosinophil cationic protein and lower levels of methacholine PC20 and pulmonary function; favorable response to montelukast alone was associated with younger age and shorter disease duration. Greater differential response to fluticasone over montelukast was associated with higher bronchodilator use, bronchodilator response, exhaled nitric oxide levels, and eosinophil cationic protein levels and lower methacholine PC20 and pulmonary function values. Conclusions: Response to fluticasone and montelukast vary considerably. Children with low pulmonary function or high levels of markers associated with allergic inflammation should receive ICS therapy. Other children could receive either ICSs or LTRAs.
AB - Background: Responses to inhaled corticosteroids (ICSs) and leukotriene receptor antagonists (LTRAs) vary among asthmatic patients. Objective: We sought to determine whether responses to ICSs and LTRAs are concordant for individuals or whether asthmatic patients who do not respond to one medication respond to the other. Methods: Children 6 to 17 years of age with mild-to-moderate persistent asthma were randomized to one of 2 crossover sequences, including 8 weeks of an ICS, fluticasone propionate (100 μg twice daily), and 8 weeks of an LTRA, montelukast (5-10 mg nightly depending on age), in a multicenter, double-masked, 18-week trial. Response was assessed on the basis of improvement in FEV1 and assessed for relationships to baseline asthma phenotype-associated biomarkers. Results: Defining response as improvement in FEV1 of 7.5% or greater, 17% of 126 participants responded to both medications, 23% responded to fluticasone alone, 5% responded to montelukast alone, and 55% responded to neither medication. Compared with those who responded to neither medication, favorable response to fluticasone alone was associated with higher levels of exhaled nitric oxide, total eosinophil counts, levels of serum IgE, and levels of serum eosinophil cationic protein and lower levels of methacholine PC20 and pulmonary function; favorable response to montelukast alone was associated with younger age and shorter disease duration. Greater differential response to fluticasone over montelukast was associated with higher bronchodilator use, bronchodilator response, exhaled nitric oxide levels, and eosinophil cationic protein levels and lower methacholine PC20 and pulmonary function values. Conclusions: Response to fluticasone and montelukast vary considerably. Children with low pulmonary function or high levels of markers associated with allergic inflammation should receive ICS therapy. Other children could receive either ICSs or LTRAs.
KW - Asthma
KW - Biomarkers
KW - Exhaled nitric oxide
KW - Fluticasone propionate
KW - Inhaled corticosteroids
KW - Montelukast
KW - Pulmonary response
UR - http://www.scopus.com/inward/record.url?scp=13444254245&partnerID=8YFLogxK
U2 - 10.1016/j.jaci.2004.11.014
DO - 10.1016/j.jaci.2004.11.014
M3 - Article
C2 - 15696076
AN - SCOPUS:13444254245
SN - 0091-6749
VL - 115
SP - 233
EP - 242
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 2
ER -