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Choline May Help Cystic Fibrosis Patients

04/09/2007

VANCOUVER— A 14-day intervention found dietary supplementation with choline-related compounds improves a low S-adenosylmethionine to Sadenosylhomocysteine (SAM:SAH) ratio and glutathione balance in juvenile cystic fibrosis patients. The study, conducted by researchers from the University of British Columbia and University of Arkansas for Medical Sciences, randomly assigned children with CF to one of three treatment groups—the first received 2 g/d lecithin;

the second received 2 g/d choline; and the third received 2 g/d choline. The control group was healthy children without CF. Researchers then evaluated plasma homocysteine levels in each group by measuring methionine, adenosine, cysteine, cysteinyl-glycine, glutathione, glutathione disulfide (GSSG), and fatty acids, in addition to testing for SAM:SAH and red blood cell phospholipid concentrations.

They found supplementation with lecithin, choline or betaine resulted in a significant increase in plasma methionine, SAM, SAM:SAH and glutathione:GSSG, and a decrease in SAH. These positive upward swings in the SAM:SAH ratio and methionine levels led researchers to conclude choline and related supplements could benefit juvenile cystic fibrosis patients.

The study was published in the American Journal of Clinical Nutrition (85, 3, 702-708, 2007).


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