Background The 2022 Global Initiative for Asthma guidelines emphasise the inhaled long-acting beta(2)-agonist formoterol as part of the first treatment step, and therefore formoterol use among athletes will probably increase. However, prolonged supratherapeutic use of inhaled beta(2)-agonists impairs training outcomes in moderately trained men. We investigated whether inhaled formoterol, at therapeutic doses, imposes detrimental effects in endurance-trained individuals of both sexes.Methods 51 endurance-trained participants (31 male, 20 female; mean +/- SD maximal oxygen consumption ((V) over dot (O2max)) 62 +/- 6 mL center dot min(-1)center dot kg bw(-1) and 52 +/- 5 mL center dot min(-1)center dot kg bw(-1), respectively) inhaled formoterol (24 mu g; n=26) or placebo (n=25) twice daily for 6 weeks. At baseline and follow-up, we assessed (V) over dot (O2max) and incremental exercise performance during a bike-ergometer ramp-test; body composition by dual-energy X-ray absorptiometry; muscle oxidative capacity by high-resolution mitochondrial respirometry, enzymatic activity assays and immunoblotting; intravascular volumes by carbon monoxide rebreathing; and cardiac left ventricle mass and function by echocardiography.Results Compared to placebo, formoterol increased lean body mass by 0.7 kg (95% CI 0.2-1.2 kg; treatmentxtrial p=0.022), but decreased (V) over dot(O2max) by 5% (treatmentxtrial p=0.013) and incremental exercise performance by 3% (treatmentxtrial p<0.001). In addition, formoterol lowered muscle citrate synthase activity by 15% (treatmentxtrial p=0.063), mitochondrial complex II and III content (treatmentxtrial p=0.028 and p=0.007, respectively), and maximal mitochondrial respiration through complexes I and I+II by 14% and 16% (treatmentxtrial p=0.044 and p=0.017, respectively). No apparent changes were observed in cardiac parameters and intravascular blood volumes. All effects were sex-independent.Conclusion Our findings demonstrate that inhaled therapeutic doses of formoterol impair aerobic exercise capacity in endurance-trained individuals, which is in part related to impaired muscle mitochondrial oxidative capacity. Thus, if low-dose formoterol fails to control respiratory symptoms in asthmatic athletes, physicians may consider alternative treatment options.

Inhaled formoterol impairs aerobic exercise capacity in endurance-trained individuals: a randomised controlled trial

Di Credico, Andrea;Hostrup, Morten
2023-01-01

Abstract

Background The 2022 Global Initiative for Asthma guidelines emphasise the inhaled long-acting beta(2)-agonist formoterol as part of the first treatment step, and therefore formoterol use among athletes will probably increase. However, prolonged supratherapeutic use of inhaled beta(2)-agonists impairs training outcomes in moderately trained men. We investigated whether inhaled formoterol, at therapeutic doses, imposes detrimental effects in endurance-trained individuals of both sexes.Methods 51 endurance-trained participants (31 male, 20 female; mean +/- SD maximal oxygen consumption ((V) over dot (O2max)) 62 +/- 6 mL center dot min(-1)center dot kg bw(-1) and 52 +/- 5 mL center dot min(-1)center dot kg bw(-1), respectively) inhaled formoterol (24 mu g; n=26) or placebo (n=25) twice daily for 6 weeks. At baseline and follow-up, we assessed (V) over dot (O2max) and incremental exercise performance during a bike-ergometer ramp-test; body composition by dual-energy X-ray absorptiometry; muscle oxidative capacity by high-resolution mitochondrial respirometry, enzymatic activity assays and immunoblotting; intravascular volumes by carbon monoxide rebreathing; and cardiac left ventricle mass and function by echocardiography.Results Compared to placebo, formoterol increased lean body mass by 0.7 kg (95% CI 0.2-1.2 kg; treatmentxtrial p=0.022), but decreased (V) over dot(O2max) by 5% (treatmentxtrial p=0.013) and incremental exercise performance by 3% (treatmentxtrial p<0.001). In addition, formoterol lowered muscle citrate synthase activity by 15% (treatmentxtrial p=0.063), mitochondrial complex II and III content (treatmentxtrial p=0.028 and p=0.007, respectively), and maximal mitochondrial respiration through complexes I and I+II by 14% and 16% (treatmentxtrial p=0.044 and p=0.017, respectively). No apparent changes were observed in cardiac parameters and intravascular blood volumes. All effects were sex-independent.Conclusion Our findings demonstrate that inhaled therapeutic doses of formoterol impair aerobic exercise capacity in endurance-trained individuals, which is in part related to impaired muscle mitochondrial oxidative capacity. Thus, if low-dose formoterol fails to control respiratory symptoms in asthmatic athletes, physicians may consider alternative treatment options.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11564/842736
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