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Volume 25, Issue 11, Pages 1115-1119 (November 2009)


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Ingestion of ferrous sulfate increases ferremia in patients with short bowel syndrome

Fabíola Rainato Gabriel, M.D.Corresponding Author Informationemail address, Vivian M.M. Suen, Ph.D., Julio Sergio Marchini, Ph.D., José Eduardo Dutra de Oliveira, Ph.D.

Received 29 October 2008; accepted 20 January 2009. published online 21 May 2009.

Abstract 

Objective

Because short bowel syndrome is associated with iron deficiency, the objective of the present study was to monitor ferremia after the ingestion of different iron compounds and doses in enterectomized patients.

Methods

This was a randomized, double-blind, cross-over study conducted in 13 patients of both sexes in the metabolic unit of Hospital das Clínicas de Faculdade de Medicina de Ribeirão Preto-Universídade de São Paulo and was divided into two stages. Three different iron compounds, ferrous sulfate (FS), sodium iron ethylenediaminetetra-acetic acid (EDTA), and dehydrated cell fraction (DCF), were studied. The patients were randomly assigned to one of four groups receiving high-dose DCF (120mg) and low-dose DCF (5mg) and the two iron compounds. The subjects (n=7) receiving high-dose DCF participated in 2 test days. All patients receiving the physiologic dose (low-dose DCF, n=6) participated in 3 test days with a 1-mo interval between compounds. After an 8-h fast, blood samples were collected at 0.25, 0.5, 1, and 2h. Serum iron curve and the sum of the area under the curve were calculated and adjusted according to a mixed-effect linear model (P<0.05).

Results

Serum FS levels were higher in the 120-mg group compared with the others (P<0.005). The mean areas under the curve for FS and EDTA at the doses of 120 and 5mg of elemental iron were 238, 224, 177, and 153 μg/dL, respectively. The mean area under the curve for DCF was 165 μg/dL, with no significant difference between groups.

Conclusion

Regardless of dose, FS was the compound that resulted in higher ferremia compared with the other doses and compounds.

Division of Clinical Nutrition, Department of Internal Medicine, Ribeirão Preto School of Medicine, São Paulo University Ribeirao Preto, Sao Paulo, Brazil

Corresponding Author InformationCorresponding author. Tel.: +55-16-3602-3375; fax: +55-16-3633-6695.

PII: S0899-9007(09)00124-5

doi:10.1016/j.nut.2009.01.019


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