4.7 Article

Breast-milk iodine concentration declines over the first 6 mo postpartum in iodine-deficient women

Journal

AMERICAN JOURNAL OF CLINICAL NUTRITION
Volume 92, Issue 4, Pages 849-856

Publisher

OXFORD UNIV PRESS
DOI: 10.3945/ajcn.2010.29630

Keywords

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Funding

  1. Otago Research Grant
  2. Laurenson's Fund

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Background: Little is known about the iodine status of lactating mothers and their infants during the first 6 mo postpartum or, if deficient, the amount of supplemental iodine required to improve status. Objective: The objective was to determine maternal and infant iodine status and the breast-milk iodine concentration (BMIC) over the first 6 mo of breastfeeding. Design: A randomized, double-blind, placebo-controlled supplementation trial was conducted in lactating women who received placebo (n = 56), 75 mu g I/d (n = 27), or 150 mu g I/d (n = 26) after their infants' birth until 24 wk postpartum. Maternal and infant urine samples and breast-milk samples were collected at 1, 2, 4, 8, 12, 16, 20, and 24 wk. Maternal serum thyrotropin and free thyroxine concentrations were measured at 24 wk. Results: Over 24 wk, the median urinary iodine concentration (UIC) of unsupplemented women and their infants ranged from 20 to 41 mu/L and 34 to 49 mu g/L, respectively, which indicated iodine deficiency (ie, UIC < 100 mu g/L). Mean maternal UIC was 2.1-2.4 times higher in supplemented than in unsupplemented women (P < 0.001) but did not differ significantly between the 2 supplemented groups. BMIC in the placebo group decreased by 40% over 24 wk (P < 0.001) and was 1.3 times and 1.7 times higher in women supplemented with 75 mu g I/d (P = 0.030) and 150 mu g I/d (P < 0.001), respectively, than in unsupplemented women. Thyrotropin and free thyroxine did not differ significantly between groups. Conclusion: BMIC decreased in the first 6 mo in these iodine-deficient lactating women; supplementation with 75 or 150 mu g I/d increased the BMIC but was insufficient to ensure adequate iodine status in women or their infants. The study was registered with the Australian New Zealand Clinical Trials Registry as ACTRN12605000345684. Am J Clin Nutr 2010;92:849-56.

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