Literature DB >> 3136639

Short-term nutritional supplementation during management of pulmonary exacerbations in cystic fibrosis: a controlled study, including effects of protein turnover.

R W Shepherd1, T L Holt, G Cleghorn, L C Ward, A Isles, P Francis.   

Abstract

Effects of nutritional supplements on minimizing weight loss and abnormalities of protein turnover during pulmonary exacerbations in cystic fibrosis (CF) were studied by controlled trial. Patients received pulmonary therapy and either standard diet (n = 10) or adjunctive enteral supplements (n = 12). Initial protein turnover, measured by [15N]glycine kinetics, showed alterations of protein synthesis (P Syn) and catabolism (P Cat), which correlated with the degree of underweight, and negligible net protein deposition (P Dep). With treatment both groups had significant increases in mean body weight and forced expiratory volume in 1 s, expressed as percent predicted value for height (FEV1) by 3 wk, but a significant correlation between initial underweight and subsequent weight gain was observed only in supplemented patients. Mean P Syn and P Dep increased significantly (p less than 0.001) only in the supplemented group. Pulmonary exacerbations in CF have important adverse effects on body-protein metabolism, similar to changes in protein-energy malnutrition and infection. These effects are reversed by short-term nutritional support. Strategic nutritional intervention should thus be considered in management, especially in malnourished patients.

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Year:  1988        PMID: 3136639     DOI: 10.1093/ajcn/48.2.235

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


  13 in total

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3.  Free 25-Hydroxyvitamin D Concentrations in Cystic Fibrosis.

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4.  Nutritional impact of antipseudomonas intravenous antibiotic courses in cystic fibrosis.

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Review 5.  Nutrition support in hospitalised adults at nutritional risk.

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6.  Influence of gender and interleukin-10 deficiency on the inflammatory response during lung infection with Pseudomonas aeruginosa in mice.

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7.  Long-term survival and nutritional data in patients with cystic fibrosis treated in a Danish centre.

Authors:  M Nir; S Lanng; H K Johansen; C Koch
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8.  Dietary essential amino acids are highly anabolic in pediatric patients with cystic fibrosis.

Authors:  Mariëlle P K J Engelen; Gulnur Com; Robert R Wolfe; Nicolaas E P Deutz
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9.  Variations in asthma hospitalizations and deaths in New York City.

Authors:  W Carr; L Zeitel; K Weiss
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Review 10.  Exacerbations in cystic fibrosis: 2 . prevention.

Authors:  Scott C Bell; Philip J Robinson
Journal:  Thorax       Date:  2007-08       Impact factor: 9.139

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