Department of Internal Medicine, Mashhad Medical Sciences Branch, Islamic Azad University, Mashhad, Iran AND Health Policy Research Centre, Institute of Health, Shiraz University of Medical Sciences, Shiraz, Iran.
3 Department of Internal Medicine, Medical School, Islamic Azad University, Mashhad Branch, Mashhad, Iran.
Iran J Allergy Asthma Immunol. 2023 Feb 20;22(1):1-11. doi: 10.18502/ijaai.v22i1.12000.
The purpose of this study was to evaluate the effect of 8 months of treatment with itraconazole on airway wall thickness in patients with severe persistent asthma. It was a double-blind, randomized, placebo-controlled clinical trial (IRCT20091111002695N9). Seventy-five subjects with severe persistent asthma received itraconazole (100 mg), prednisolone (5 mg), or placebo twice a day for eight months in three treatment groups (n=25 in each group). The primary objective was to improve the right upper lobe apical segmental bronchus (RB1) wall thickness percentage measured by high-resolution computed tomography scan of the lungs. Other morphometric measurements of RB1, asthma control test (ACT) score, presence of wheezing, dyspnea severity, rate of asthma exacerbation, fractional exhaled nitric oxide (FeNO), and expiratory volume in 1 second (FEV1) were set as the secondary outcomes. Wall thickness percentage reduced significantly from 46% to 43.7% from pre- to post-treatment in the itraconazole-treated subjects. Similarly, lumen area and radius increased significantly in both the prednisolone and itraconazole groups. Itraconazole led to a significant improvement in wheezing, dyspnea severity, FEV1, ACT score, and FeNO. Although prednisolone was also effective in improving pulmonary function tests and ACT scores, it was associated with significantly more side effects than itraconazole. Long-term treatment with itraconazole resulted in a significant reduction in bronchial wall thickness and improvements in clinical findings and pulmonary function tests. Thus, itraconazole could be a helpful add-on treatment option for severe persistent asthma patients to achieve better disease control.
本研究旨在评估伊曲康唑治疗 8 个月对重度持续性哮喘患者气道壁厚度的影响。这是一项双盲、随机、安慰剂对照的临床试验(IRCT20091111002695N9)。75 例重度持续性哮喘患者随机分为三组,分别接受伊曲康唑(100mg)、泼尼松(5mg)或安慰剂,每日两次,治疗 8 个月(每组 25 例)。主要终点是改善肺部高分辨率计算机断层扫描测量的右上叶尖段支气管(RB1)壁厚度百分比。其他 RB1 的形态学测量、哮喘控制测试(ACT)评分、哮鸣音、呼吸困难严重程度、哮喘加重率、呼出气一氧化氮(FeNO)和 1 秒呼气量(FEV1)也作为次要结局。与治疗前相比,伊曲康唑治疗组的 RB1 壁厚度百分比从 46%降至治疗后的 43.7%。同样,泼尼松和伊曲康唑组的管腔面积和半径均显著增加。伊曲康唑可显著改善哮鸣音、呼吸困难严重程度、FEV1、ACT 评分和 FeNO。尽管泼尼松也能有效改善肺功能测试和 ACT 评分,但与伊曲康唑相比,它的副作用明显更多。长期伊曲康唑治疗可显著减轻支气管壁厚度,并改善临床和肺功能测试结果。因此,伊曲康唑可能是重度持续性哮喘患者实现更好疾病控制的一种有益的附加治疗选择。