Wang Ran, Maidstone Robert, Singh Dave, Ray David, Loudon Andrew S, Simpson Angela, Durrington Hannah Jane
NIHR Manchester Biomedical Research Centre, Manchester, UK.
School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Thorax. 2025 Jul 15;80(8):504-511. doi: 10.1136/thorax-2024-222073.
Asthma demonstrates a robust daily rhythm, with airflow obstruction and airway inflammation peaking overnight. Aligning the timing of drug administration with rhythms in disease (chronotherapy) may improve therapeutic efficacy. We aimed to evaluate the impact of dosage timing for inhaled corticosteroids in asthma.
This is a randomised three-way crossover trial. Participants with mild to moderate atopic asthma were randomised to beclometasone dipropionate: (1) 400 µg once daily between 08:00 and 09:00 (OD); (2) 400 µg once daily between 15:00 and 16:00 (OD); and (3) 200 µg twice daily between 08:00 and 09:00 and between 20:00 and 21:00 (BD) for 28 days, with a 2 week washout period in between treatment periods. Six-hourly spirometry and biomarkers were measured over 24 hours following the run-in period and at the end of each treatment period.
Of 25 participants, 21 completed all regimens. OD was superior in improving 22:00 FEV (median (IQR): +160 (+70, +270) ml) compared with OD (-20 (-80, +230) ml) and BD (+80 (-20, +200) ml). OD resulted in better overnight (22:00 and 04:00) suppression in blood eosinophil counts compared with BD and OD. All regimens improved asthma control and reduced fractional exhaled nitric oxide and serum cortisol levels with no difference among dosing regimens.
OD better suppresses the nocturnal dip in lung function and peak of blood eosinophil counts compared with BD and OD; this was without an increase in adverse events. Future trials are warranted to validate these findings in real-life settings and to determine which population may best benefit from chronotherapy.
哮喘呈现出明显的每日节律,气流阻塞和气道炎症在夜间达到峰值。使药物给药时间与疾病节律(时间疗法)相匹配可能会提高治疗效果。我们旨在评估吸入性糖皮质激素给药时间对哮喘的影响。
这是一项随机三交叉试验。轻度至中度特应性哮喘患者被随机分为倍氯米松二丙酸酯组:(1)每日一次,400µg,于08:00至09:00给药(OD);(2)每日一次,400µg,于15:00至16:00给药(OD);(3)每日两次,200µg,分别于08:00至09:00和20:00至21:00给药(BD),持续28天,各治疗期之间有2周的洗脱期。在导入期结束后以及每个治疗期结束时,在24小时内每6小时进行一次肺活量测定和生物标志物检测。
25名参与者中,21名完成了所有治疗方案。与OD(-20(-80,+230)ml)和BD(+80(-20,+200)ml)相比,OD在改善22:00时的第一秒用力呼气容积(FEV)方面更优(中位数(四分位间距):+160(+70,+270)ml)。与BD和OD相比,OD导致夜间(22:00和04:00)血液嗜酸性粒细胞计数抑制效果更好。所有治疗方案均改善了哮喘控制情况,并降低了呼出一氧化氮分数和血清皮质醇水平,各给药方案之间无差异。
与BD和OD相比,OD能更好地抑制肺功能夜间下降和血液嗜酸性粒细胞计数峰值;且未增加不良事件。未来有必要进行试验,在实际环境中验证这些发现,并确定哪些人群可能从时间疗法中获益最大。