Birmingham Regional Severe Asthma Service, Heartlands Hospital and University of Birmingham, Birmingham, England.
Respiratory Department, James Cook University Hospital, Middlesbrough, England.
Ann Allergy Asthma Immunol. 2017 Apr;118(4):445-451. doi: 10.1016/j.anai.2017.02.004.
Bronchial airway inflammation is the hallmark of asthma, which may be driven by an imbalance between oxidative stress and antioxidant defenses. Antioxidants deficiency may play a role, but this has remained unconfirmed.
To evaluate the oxidative stress burden and antioxidants defenses in patients with increasing asthma severity.
This prospective case-control study compared fractional exhaled nitric oxide (FeNO), exhaled breath condensate nitrite/nitrate (EBC-NOx), spirometry, and serum vitamins and trace elements among patients with and without asthma.
Sixty participants were recruited (30 with severe asthma number; 23 women [76.7%]; mean age, 41.4 years; mean forced expiratory volume in 1 second [FEV], 2.2 L [72.2% predicted]; mean inhaled corticosteroid dosage, 2,540 μg/d; 18/30 [60%] receiving maintenance oral corticosteroids; 15 with mild asthma; all corticosteroids naïve; 9 women [60%]; mean age, 34.6 years; mean FEV, 3.48 L [100.5% predicted]; 15 healthy controls; 12 women [80%]; mean age, 37.6 years; and mean FEV, 3.53 L [111.7% predicted]). The mean FeNO levels increased significantly with increasing asthma severity (P = .01), but the EBC-NOx levels did not change significantly (P = .90). Paradoxically, vitamin A and vitamin E increased with increased disease severity, with vitamin E levels increasing significantly (P = .07 and P < .001, respectively). There was no significant difference between groups in the levels of copper (P = .37), zinc (P = .97), or selenium (P = .90).
FeNO but not EBC-NOx is increased significantly with asthma severity with no evidence of vitamins or trace elements deficiency in severe asthma. Impaired oxidative stress defenses in severe asthma may be driven by factors other than vitamins or trace elements deficiency.
支气管气道炎症是哮喘的标志,其可能由氧化应激与抗氧化防御之间的失衡驱动。抗氧化剂缺乏可能起作用,但这一点尚未得到证实。
评估哮喘严重程度增加的患者的氧化应激负担和抗氧化防御能力。
这项前瞻性病例对照研究比较了呼出气一氧化氮分数(FeNO)、呼气冷凝液亚硝酸盐/硝酸盐(EBC-NOx)、肺量计检查以及哮喘患者和非哮喘患者的血清维生素和微量元素。
共招募了 60 名参与者(30 名严重哮喘患者;23 名女性[76.7%];平均年龄 41.4 岁;平均 1 秒用力呼气量(FEV1)2.2 L[72.2%预计值];平均吸入皮质类固醇剂量 2540 μg/d;18/30 名[60%]患者接受维持口服皮质类固醇治疗;15 名轻度哮喘患者;均未使用皮质类固醇;9 名女性[60%];平均年龄 34.6 岁;平均 FEV1 3.48 L[100.5%预计值];15 名健康对照者;12 名女性[80%];平均年龄 37.6 岁;平均 FEV1 3.53 L[111.7%预计值])。随着哮喘严重程度的增加,FeNO 水平显著升高(P=0.01),但 EBC-NOx 水平没有显著变化(P=0.90)。矛盾的是,随着疾病严重程度的增加,维生素 A 和维生素 E 水平增加,维生素 E 水平显著增加(P=0.07 和 P<0.001)。各组之间铜(P=0.37)、锌(P=0.97)或硒(P=0.90)的水平无显著差异。
随着哮喘严重程度的增加,FeNO 显著升高,但严重哮喘中没有证据表明存在维生素或微量元素缺乏。严重哮喘中氧化应激防御受损的原因可能不是维生素或微量元素缺乏。