Advertisement
Journal Home
Search for

Volume 21, Issue 9, Pages 895-900 (September 2005)


View previous. 2 of 17 View next.

Patients with severe bowel malabsorption do not have changes in iodine status

Anderson Marilere Navarro, M.Nutr.S.aCorresponding Author Informationemail address, Vivian Marques Miguel Suen, Ph.D.a, Isabel Machado Souza, Pharm.G.b, José Eduardo Dutra De Oliveira, Ph.D.a, Julio Sergio Marchini, Ph.D.a

Received 7 November 2004; accepted 5 February 2005. published online 27 June 2005.

Abstract 

Objective

We evaluated the influence of intestinal malabsorption on iodine status in patients who had short gut syndrome and received total parenteral nutrition (group I) compared with control subjects who had eutrophia (group II) and patients who had other illnesses but normal digestive tracts (group III).

Methods

Twenty-seven subjects were studied. Iodine intake was determined by the measurement of iodine in ingested food and in parenteral nutrition solutions. Urinary iodine excretion was measured by the Sandell-Kalthoff reaction. Urinary creatinine, anthropometric, and thyroid hormone functions were also determined.

Results

Daily iodine intakes were 658 ± 125 (mean ± standard deviation), 573 ± 204, and 629 ± 208 μg for groups I, II, and III, respectively. Daily urinary iodine excretion levels were 399 ± 308, 439 ± 192, and 370 ± 268 μg and ratios of urinary iodine (micrograms) to creatinine (grams) were 614 ± 349, 354 ± 142, and 483 ± 292, respectively. There were no statistically significant differences across groups.

Conclusion

In Brazil the iodine provided by food, including iodized salt, has been sufficient to maintain iodine status in patients with short gut syndrome.

a Division of Clinical Nutrition, Department of Clinical Medicine, Medical School of Ribeirão Preto, University of São Paulo, São Paulo, Brazil

b Pediatrics Laboratory, University Hospital, Medical School of Ribeirão Preto, University of São Paulo, Ribeirao Preto, São Paulo, Brazil

Corresponding Author InformationCorresponding author. Tel.: +55-16-602-3187; fax: +55-16-633-6695.

 This study was financed in part by FAPESP process 98/03598-2.

PII: S0899-9007(05)00166-8

doi:10.1016/j.nut.2005.02.006


View previous. 2 of 17 View next.

Advertisement