A pilot study on the safety and efficacy of a novel antioxidant rich formulation in patients with cystic fibrosis

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• 作者：Konstantinos A. Papas ; Marci K. Sontag ; Churee Pardee ; Ronald J. Sokol ; Scott D. Sagel ; Frank J. Accurso ; Jeffrey S. Wagener
• 关键词：Cystic fibrosis ; Antioxidant ; Malabsorption ; Beta-carotene ; Inflammatory markers ; Coenzyme Q10 ; Gamma-tocopherol ; Induced sputum ; Pancretic insufficiency
• 刊名：Journal of Cystic Fibrosis
• 出版年：2008
• 出版时间：January 2008
• 年：2008
• 卷：7
• 期：1
• 页码：60-67
• 全文大小：318 K

文摘

Pancreatic insufficiency and a diminished bile acid pool cause malabsorption of important essential nutrients and other dietary components in cystic fibrosis (CF). Of particular significance is the malabsorption of fat-soluble antioxidants such as carotenoids, tocopherols and coenzyme Q<sub>10sub> (CoQ<sub>10sub>). Despite supplementation, CF patients are often deficient in these compounds, resulting in increased oxidative stress, which may contribute to adverse health effects. This pilot study was designed to evaluate the safety of a novel micellar formulation (CF-1) of fat-soluble nutrients and antioxidants and to determine its efficacy in improving plasma levels of these compounds and reducing inflammatory markers in induced sputum.

ss=""h4"">Methods

Ten CF subjects, ages 8 to 45 years old, were given orally 10 ml of the CF-1 formulation daily for 56 days after a 21-day washout period in which subjects stopped supplemental vitamin use except for a standard multivitamin. Plasma obtained at − 3, 0 (baseline), 1, 2, 4, and 8 weeks was assayed for β-carotene, γ-tocopherol, retinol, and CoQ<sub>10sub> as well as for safety parameters (comprehensive metabolic panel and complete blood count). In addition, pulmonary function was measured and induced sputum was assayed for markers of inflammation and quantitative bacterial counts both prior and during dosing.

ss=""h4"">Results

No serious adverse effects, laboratory abnormalities or elevated nutrient levels (above normal) were identified as related to CF-1. Supplementation with CF-1 significantly increased β-carotene levels at all dosing time points when compared to screening and baseline. In addition, γ-tocopherol and CoQ<sub>10sub> significantly increased from baseline in all subjects. Induced sputum myeloperoxidase significantly decreased and there was a trend toward decreases in PMN elastase and total cell counts with CF-1. There was a significant inverse correlation between the antioxidant levels and induced sputum changes in IL-8 and total neutrophils. Lung function and sputum bacterial counts were unchanged.

ss=""h4"">Conclusion

The novel CF-1 formulation safely and effectively increased plasma levels of important fat-soluble nutrients and antioxidants. In addition, improvements in antioxidant plasma levels were associated with reductions in airway inflammation in CF patients.