Lombardi Carlo, Berti Alvise, Cottini Marcello, Roca Elena, Ventura Laura
Departmental Unit of Allergology, Immunology and Pulmonary Diseases, Fondazione Poliambulanza, Brescia, Italy.
Center for Medical Sciences (CISMed), Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.
ERJ Open Res. 2023 Oct 2;9(5). doi: 10.1183/23120541.00114-2023. eCollection 2023 Sep.
Severe asthma limits exercise to avoid respiratory symptoms. The objective of the present study was to investigate the role of the 6-min walk test (6MWT) in severe asthma.
Consecutive patients with severe eosinophilic asthma were enrolled. A 6MWT was performed before and after 12 months. Inhaled therapy dose, oral corticosteroids dose, pulmonary function tests, eosinophil blood count, fractional exhaled nitric oxide (), Asthma Control Test (ACT) score and responses to the Asthma Quality of Life Questionnaire (AQLQ) were also recorded.
Of the 22 patients enrolled, 13 were treated with mepolizumab 100 mg every 4 weeks in addition to conventional therapy and nine with conventional therapy only. The majority of the patients were treated with high-dose inhaled corticosteroids/long-acting β-agonists/long-acting muscarinic receptor antagonists, while approximately half were on continuous oral corticosteroids. After 12 months, the mepolizumab group only showed a significant improvement in pulmonary function tests (percentage forced expiratory volume in 1 s and percentage forced expiratory flow at 25-75% forced vital capacity (FEF), both p<0.001; percentage forced vital capacity, p<0.01) and clinical laboratory parameters (eosinophil count, measured at a flow rate of 50 mL·s, ACT and AQLQ, p<0.001). No significant changes in the proportion of patients using continuous oral corticosteroids and high-dose inhaled corticosteroids/long-acting β-agonists/long-acting muscarinic receptor antagonists were observed in either group (p>0.05). By paired comparisons, statistically significant improvements of the mean 6-min walk distance (6MWD) were observed in the mepolizumab (p<0.001) and conventional therapy (p<0.01) groups, while no improvement was seen in dyspnoea Borg scale, heart rate, percentage oxygen saturation or systolic and diastolic blood pressure. 6MWD showed significant direct correlations with ACT (r=0.5998, p<0.001), AQLQ (r=0.3978, p=0.009) and FEF (r=0.3589, p=0.017).
The 6MWT could complement severe asthma assessment and be relevant in evaluating the objective response to treatment, including biological therapies like mepolizumab.
重度哮喘患者会限制运动以避免出现呼吸道症状。本研究的目的是调查6分钟步行试验(6MWT)在重度哮喘中的作用。
纳入连续性重度嗜酸性粒细胞性哮喘患者。在12个月前后分别进行一次6MWT。同时记录吸入治疗剂量、口服糖皮质激素剂量、肺功能测试、嗜酸性粒细胞计数、呼出一氧化氮分数()、哮喘控制测试(ACT)评分以及哮喘生活质量问卷(AQLQ)的反应情况。
纳入的22例患者中,13例在接受常规治疗的基础上每4周接受100mg美泊利单抗治疗,9例仅接受常规治疗。大多数患者接受高剂量吸入性糖皮质激素/长效β受体激动剂/长效毒蕈碱受体拮抗剂治疗,约一半患者持续口服糖皮质激素。12个月后,美泊利单抗组仅在肺功能测试(第1秒用力呼气容积百分比和用力肺活量25%-75%时的用力呼气流量百分比(FEF),均p<0.001;用力肺活量百分比,p<0.01)和临床实验室参数(嗜酸性粒细胞计数、在50mL·s流速下测量的、ACT和AQLQ,p<0.001)方面有显著改善。两组中使用持续口服糖皮质激素以及高剂量吸入性糖皮质激素/长效β受体激动剂/长效毒蕈碱受体拮抗剂的患者比例均无显著变化(p>0.05)。通过配对比较,美泊利单抗组(p<0.001)和常规治疗组(p<0.01)的平均6分钟步行距离(6MWD)有统计学意义的显著改善,而呼吸困难Borg量表、心率、血氧饱和度百分比或收缩压和舒张压均无改善。6MWD与ACT(r=0.5998,p<0.001)、AQLQ(r=0.3978,p=0.009)和FEF(r=0.3589,p=0.017)呈显著正相关。
6MWT可补充重度哮喘评估,并有助于评估包括美泊利单抗等生物疗法在内的治疗客观反应。