Exhaled ethane, a marker of lipid peroxidation, is elevated in chronic obstructive pulmonary disease

被引:211
|
作者
Paredi, P
Kharitonov, SA
Leak, D
Ward, S
Cramer, D
Barnes, PJ
机构
[1] Natl Heart & Lung Inst, Dept Thorac Med, Imperial Coll, Sch Med, London SW3 6LY, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Biochem, London, England
[3] Royal Brompton Hosp, Lung Funct Unit, London SW3 6LY, England
关键词
D O I
10.1164/ajrccm.162.2.9909025
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Ethane is a product of lipid peroxidation and can be measured in the exhaled air as an index of oxidative stress. Oxidant/antioxidant imbalance is important in the pathogenesis of chronic obstructive pulmonary disease (COPD). Therefore, we measured exhaled ethane in 22 patients with COPD (mean age +/- SEM, 59 +/- 8 yr; 19 male) and compared it with other noninvasive markers of oxidative stress and inflammation such as carbon monoxide (CO), measured electrochemically, and nitric oxide (NO), measured by chemiluminescence. Exhaled ethane was collected during a flow and pressure-controlled exhalation into a reservoir, discarding dead space air contaminated with ambient air. A sample of the collected expired air was analyzed by chromatography. Compared with normal subjects (n = 14; eight men; age, 33 +/- 2.8 yr), patients with COPD not on steroid treatment (n = 12; FEV1, 58 +/- 6%) had elevated levels of exhaled ethane (2.77 +/- 0.25 and 0.88 +/- 0.09 ppb, respectively, p < 0.05), CO (5.96 +/- 0.50 and 2.8 +/- 0.25 ppm, p < 0.05) and NO (11.86 +/- 0.53 and 6.77 +/- 0.50 ppb, p < 0.05) levels. Ethane was correlated to FEV1 (r = -0.67, p < 0.05). Patients receiving steroid treatment (n = 10; FEV1, 56 +/- 2%) had lower levels of ethane (0.48 +/- 0.05 ppb) than did steroid-treated patients, whereas CO (5.99 +/- 0.63 ppm) and NO (9.11 +/- 0.53 ppb) levels were similar in the two treatment groups. Exhaled ethane is elevated, correlates with FEV1, and is significantly lower in patients treated with steroids, so it may be complementary to the use of NO and CO in assessing and monitoring oxidative stress in COPD.
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收藏
页码:369 / 373
页数:5
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