Improved antioxidant and fatty acid status of patients with cystic fibrosis after antioxidant supplementation is linked to improved lung function

被引:81
作者
Wood, LG
Fitzgerald, DA
Lee, AK
Garg, ML [1 ]
机构
[1] Univ Newcastle, Discipline Nutr & Dietet, Fac Hlth, Callaghan, NSW 2308, Australia
[2] Childrens Hosp Westmead, Dept Resp Med, Sydney, NSW, Australia
[3] New Childrens Hosp, Dept Resp Med, Sydney, NSW, Australia
关键词
cystic fibrosis; oxidative stress; antioxidant supplementation; isoprostanes; fatty acids; vitamin E; vitamin C; beta-carotene; glutathione peroxidase; superoxide dismutase;
D O I
10.1093/ajcn/77.1.150
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Oxidative stress, as measured by 8-iso-prostaglandin F-2alpha (8-iso-PGF(2alpha)), and depleted antioxidant defenses were shown in stable cystic fibrosis (CF) patients. The plasma fatty acid status of CF patients was linked to oxidative stress after respiratory exacerbations. Objective: We examined changes in plasma 8-iso-PGF(2alpha), antioxidant defenses, plasma fatty acid status, and clinical markers resulting from short-term antioxidant supplementation. Design: Forty-six CF patients were randomly assigned to either group A [low dose of supplement (10 mg vitamin E and 500 mug vitamin A)] or group B [high dose of supplement (200 mg vitamin E, 300 mg vitamin C, 25 mg beta-carotene, 90 mug Se, and 500 mug vitamin A)]. Plasma concentrations of 8-iso-PGF(2alpha) vitamins E and C, P-carotene, zinc, selenium, and copper; plasma fatty acid composition; erythrocyte glutathione peroxidase (EC 1.11.1.9) and superoxide dismutase (EC 1.15.1.1) activities; lung function; and dietary intake were measured before and after 8 wk of supplementation. Results: Antioxidant defenses in group B improved, whereas those in group A did not: in groups B and A, the mean (+/-SEM) changes (Delta) in vitamin E were 10.6 +/- 1.5 and - 1.9 +/- 0.9 mumol/L, respectively (P < 0.001), Δβ-carotene were 0.1 +/- 0.04 and -0.01 +/- 0.02 μmol/L, respectively (P = 0.007), Δselenium were 0.51 +/- 0.10 and - 0.09 +/- 0.04 μmol/L, respectively (P < 0.001), and Deltaglutathione peroxidase activity were 1.3 +/- 0.3 and -0.3 +/- 0.6 U/g hemoglobin, respectively (P = 0.016). There were no significant differences between the groups in Delta8-iso-PGF(2alpha), Deltavitamin C, Deltafatty acid composition, Deltasuperoxide dismutase activity, Deltalung function, or Deltawhile cell count. Within group B, Deltabeta-carotene correlated with Deltapercentage of forced vital capacity (r = 0.586, P = 0.005), Deltaselenium correlated with Deltapercentage of forced expiratory volume in 1 s (r = 0.440, P = 0.046), and Deltaplasma fatty acid concentrations correlated with Deltapercentage of forced expiratory volume in 1 s (r = 0.583, P = 0.006) and Delta8-iso-PGF(2alpha) (r = 0.538, P = 0.010). Conclusions: Whereas increased beta-carotene, selenium, and fatty acid concentrations are linked to improved lung function, increased plasma fatty acid concentrations are linked to oxidative stress. If oxidative stress is deemed to be important to the clinical outcome of CF patients, means of reducing oxidative stress while maintaining a high-fat, high-energy diet must be investigated.
引用
收藏
页码:150 / 159
页数:10
相关论文
共 61 条
[11]  
Carr SB, 2000, J ROY SOC MED, V93, P14
[12]   In vivo lipid peroxidation and platelet activation in cystic fibrosis [J].
Ciabattoni, G ;
Davì, C ;
Collura, M ;
Iapichino, L ;
Pardo, F ;
Ganci, A ;
Romagnoli, R ;
Maclouf, J ;
Patrono, C .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (04) :1195-1201
[13]   Elevated plasma levels of F2α isoprostane in cystic fibrosis [J].
Collins, CE ;
Quaggiotto, P ;
Wood, L ;
O'Loughlin, EV ;
Henry, RL ;
Garg, ML .
LIPIDS, 1999, 34 (06) :551-556
[14]   VITAMIN STATUS IN TREATED PATIENTS WITH CYSTIC-FIBROSIS [J].
CONGDEN, PJ ;
BRUCE, G ;
ROTHBURN, MM ;
CLARKE, PCN ;
LITTLEWOOD, JM ;
KELLEHER, J ;
LOSOWSKY, MS .
ARCHIVES OF DISEASE IN CHILDHOOD, 1981, 56 (09) :708-714
[15]   A COMPARISON OF SURVIVAL, GROWTH, AND PULMONARY-FUNCTION IN PATIENTS WITH CYSTIC-FIBROSIS IN BOSTON AND TORONTO [J].
COREY, M ;
MCLAUGHLIN, FJ ;
WILLIAMS, M ;
LEVISON, H .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1988, 41 (06) :583-591
[16]   THE KINETICS OF THE AUTOXIDATION OF POLYUNSATURATED FATTY-ACIDS [J].
COSGROVE, JP ;
CHURCH, DF ;
PRYOR, WA .
LIPIDS, 1987, 22 (05) :299-304
[17]  
DANIELS LA, 1984, HUM NUTR-APPL NUTR, V38A, P110
[18]  
DURIE PR, 1989, J ROY SOC MED, V82, P11
[19]   A diet rich in fat and poor in dietary fiber increases the in vitro formation of reactive oxygen species in human feces [J].
Erhardt, JG ;
Lim, SS ;
Bode, JC ;
Bode, C .
JOURNAL OF NUTRITION, 1997, 127 (05) :706-709
[20]   OCCURRENCE AND EFFECTS OF HUMAN VITAMIN-E-DEFICIENCY - STUDY IN PATIENTS WITH CYSTIC-FIBROSIS [J].
FARRELL, PM ;
BIERI, JG ;
FRATANTONI, JF ;
WOOD, RE ;
DISANTAGNESE, PA .
JOURNAL OF CLINICAL INVESTIGATION, 1977, 60 (01) :233-241