CORRECTION article

Front. Nutr., 27 February 2024

Sec. Clinical Nutrition

Volume 11 - 2024 | https://doi.org/10.3389/fnut.2024.1376599

Corrigendum: Safe and effective delivery of supplemental iron to healthy adults: a two-phase, randomized, double-blind trial – the safe iron study

  • 1. Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, United States

  • 2. Department of Molecular Biology and Microbiology, Tufts University, Boston, MA, United States

  • 3. Department of Developmental, Molecular and Chemical Biology, Tufts University, Boston, MA, United States

  • 4. Department of Pathology, University of Cambridge, Cambridge, United Kingdom

  • 5. Department of Food Science and Human Nutrition, Iowa State University, Ames, IA, United States

In the published article, there was an error. The error involved an inconsistency between our abstract and discussion regarding the observed effects of one treatment on some secondary outcomes, GI symptoms.

A correction has been made to Abstract, subsection Results.

This section previously stated:

“Supplementation with any form of iron did not affect any primary endpoint. In Phase I, the frequency of gastrointestinal symptoms associated with FS was unaffected by dosing with MNP or weekly administration; but participants taking IHAT more frequently reported abdominal pain (27%, p < 0.008) and nausea (4%, p = 0.009) than those taking FS, while those taking ASP more frequently reported nausea (8%, p = 0.009). Surprisingly, only 9% of participants taking IHAT at 120 mg Fe/day (Phase II) reported abdominal pain and no other group reported that symptom.”

The corrected section appears below:

“Supplementation with any form of iron did not affect any primary endpoint. Regarding secondary endpoints, in Phase I participants taking IHAT more frequently reported abdominal pain (27%, p = 0.008) than other iron forms; those taking the weekly FS dose more frequently reported nausea (20%, P = 0.009) than the other forms and modes of administration. In phase II, no such differences were observed.”

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Statements

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Summary

Keywords

iron, ferrous sulfate, malarial infectivity, bacterial proliferation, gut inflammation, IHAT, fungal iron

Citation

Lewis ED, Ortega EF, Dao MC, Barger K, Mason JB, Leong JM, Osburne MS, Magoun L, Nepveux V FJ, Chishti AH, Schwake C, Quynh A, Gilhooly CH, Petty G, Guo W, Matuszek G, Pereira D, Reddy M, Wang J, Wu D, Meydani SN and Combs Jr. GF (2024) Corrigendum: Safe and effective delivery of supplemental iron to healthy adults: a two-phase, randomized, double-blind trial – the safe iron study. Front. Nutr. 11:1376599. doi: 10.3389/fnut.2024.1376599

Received

25 January 2024

Accepted

12 February 2024

Published

27 February 2024

Volume

11 - 2024

Edited and reviewed by

Johannes le Coutre, University of New South Wales, Australia

Updates

Copyright

*Correspondence: Simin N. Meydani

†Present addresses: Erin D. Lewis, KGK Science, Inc., London, Ontario, ON, Canada

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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