Controlled trial of copper supplementation during the recovery from marasmus
Author
dc.contributor.author
Castillo Durán, Carlos
Author
dc.contributor.author
Fisberg, M.
Author
dc.contributor.author
Valenzuela, A.
Author
dc.contributor.author
Castillo Durán, Carla Andrea
Author
dc.contributor.author
Egaña, J. I.
Author
dc.contributor.author
Uauy Dagach-Imbarack, Ricardo
Admission date
dc.date.accessioned
2019-01-29T14:20:45Z
Available date
dc.date.available
2019-01-29T14:20:45Z
Publication date
dc.date.issued
1983
Cita de ítem
dc.identifier.citation
American Journal of Clinical Nutrition, Volumen 37, Issue 6, 2018, Pages 898-903
Identifier
dc.identifier.issn
00029165
Identifier
dc.identifier.other
10.1093/ajcn/37.6.898
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/160500
Abstract
dc.description.abstract
To evaluate copper nutritional status and the effect of a Cu supplement during recuperation, 27 marasmic infants were selected on admission to the nutrition recovery center at the Instituto de Nutricion y Tecnologia de los Alimentos. Thirteen infants received 80 μg/kg/day of copper supplement as sulphate and the remaining a placebo. They were paired by birth weight, age, and sex. Anthropometric indices, complete blood count, ceruloplasmin, and Cu were measured on admission and at monthly intervals. Superoxide dismutase activity was measured in hypocupremic infants and was found to be low. The mean ± SE Cu levels on admission were 127 ± 10 μg/dl for the supplemented group and 137 ± 10 μg/dl for the control. We found an increase in plasma Cu to 159 and 162 μg/dl on days 30 and 60 in the supplement group, and a significant decrease after day 30 in the placebo group. The ceruloplasmin levels followed this trend. Hypocupremia was found in 30% of the placebo group and none in the supplement