Effect of suplatast tosilate, a Th2 cytokine inhibitor, on steroid-dependent asthma: a double-blind randomised study
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Tamaoki, J
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Tokyo Womens Med Univ, Sch Med, Dept Med 1, Shinjuku Ku, Tokyo 1628666, JapanTokyo Womens Med Univ, Sch Med, Dept Med 1, Shinjuku Ku, Tokyo 1628666, Japan
Tamaoki, J
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Kondo, M
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Kondo, M
Sakai, N
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Sakai, N
Aoshiba, K
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Aoshiba, K
Tagaya, E
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Tagaya, E
Nakata, J
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Nakata, J
Isono, K
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Isono, K
Nagai, A
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Nagai, A
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[1] Tokyo Womens Med Univ, Sch Med, Dept Med 1, Shinjuku Ku, Tokyo 1628666, Japan
[2] Seirei Hamamatsu Gen Hosp, Dept Internal Med, Hamamatsu, Shizuoka, Japan
[3] Kureha Gen Hosp, Dept Med, Fukushima, Japan
[4] Nagashio Hosp, Dept Med, Tokyo, Japan
[5] Kurihashi Saiseikai Hosp, Dept Pulm Med, Kurihashi, Saitama, Japan
Background Th2 cytokines play an important part in the pathogenesis of asthma. Our aim was to study the effect of suplatast tosilate, a selective Th2 cytokine inhibitor, on asthma control and asthma exacerbations during reduction of inhaled corticosteroid dose in patients with steroid-dependent asthma. Methods 85 patients with moderate to severe asthma taking high doses (greater than or equal to 1500 mu g per day) of inhaled beclometasone dipropionate, were assigned suplatast tosilate (100 mg three times daily) or placebo for 8 weeks in a double-blind, randomised, parallel-group, multicentre trial. During the first 4 weeks, other medications remained unchanged (add-on phase); during the next 4 weeks, the doses of beclometasone were halved (steroid-reduction phase). Main outcome measures were pulmonary function, asthma symptoms, and use of beta(2)-agonists. Findings Data were available from 77 patients. During the add-on phase, suplatast tosilate treatment, compared with placebo, was associated with higher forced expiratory volume in 1 s (mean difference between groups for changes from baseline at week 4, 0.20 L [95% CI 0.16-0.24], p=0.043), morning peak expiratory flow (18.6 L/min [14.1-23.1], p=0.037), and less diurnal variation in peak expiratory flow rate, asthma symptom scores (7.1[6.6-7.6], p=0.029), and serum concentrations of eosinophil cationic protein and IgE. In the steroid-reduction phase, pulmonary function, asthma symptoms, and use of beta(2)-agonist deteriorated significantly more in the placebo group than in the suplatast group. Interpretation Treatment with a Th2 cytokine inhibitor in steroid-dependent asthma improves pulmonary function and symptom control, and allows a decrease in dose of inhaled corticosteroid without significant side-effects. Some improvements in pharmacokinetics are, however, needed.