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Choline-related supplements improve abnormal plasma methionine-homocysteine metabolites and glutathione status in children with cystic fibrosis
Author(s) -
Sheila M. Innis,
A. George F. Davidson,
Stepan Melynk,
S. Jill James
Publication year - 2007
Publication title -
american journal of clinical nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.608
H-Index - 336
eISSN - 1938-3207
pISSN - 0002-9165
DOI - 10.1093/ajcn/85.3.702
Subject(s) - choline , homocysteine , methionine , glutathione , betaine , glutathione disulfide , chemistry , endocrinology , medicine , phosphatidylcholine , lecithin , phosphatidylethanolamine , phospholipid , biochemistry , biology , amino acid , membrane , enzyme
Liver triacylglycerol accumulation and oxidative stress are common in cystic fibrosis (CF) and also occur in choline deficiency. Previously, we showed an association between elevated plasma homocysteine, reduced ratios of S-adenosylmethionine to S-adenosylhomocysteine (SAM:SAH) and of phosphatidylcholine to phosphatidylethanolamine, and phospholipid malabsorption in children with CF.

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