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The effect of iron supplement on children with euthyroid goiter: a randomized placebo-controlled clinical trial
BACKGROUND: Endemic goiter is present in most parts of Iran. Iron deficiency adversely affects the physiology of thyroid. The initial steps of thyroid hormone synthesis are catalyzed by thyroperoxidases and are dependent on iron. In many developing countries, children are at high risk of both goiter...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shahid Sadoughi University of Medical Sciences
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173026/ https://www.ncbi.nlm.nih.gov/pubmed/25254085 |
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author | Ordooei, M Akbarzadeh, M Soleimanizad, R Shamsi, F Masoumi Dehshiri, R |
author_facet | Ordooei, M Akbarzadeh, M Soleimanizad, R Shamsi, F Masoumi Dehshiri, R |
author_sort | Ordooei, M |
collection | PubMed |
description | BACKGROUND: Endemic goiter is present in most parts of Iran. Iron deficiency adversely affects the physiology of thyroid. The initial steps of thyroid hormone synthesis are catalyzed by thyroperoxidases and are dependent on iron. In many developing countries, children are at high risk of both goiter and iron deficiency anemia. In addition, iron deficiency may alter central nervous system control of thyroid metabolism; andalso Iron-deficiency anemia decreases plasma concentrations of thyroxine and triiodothyronine. MATERIAL AND METHOD: We conducted a randomized, double-blind,controlled trial in 2-12-y-old children with euthyroid goiter and without iron-deficiency anemia. The children weredivided into two groups: The Patients who were under treatment with ferrous-sulphat and controls .active treatment consisted of iron supplementation was administered orally with a dose of 2 mg/kg day. The duration of active treatment was 12 weeks. RESULTS: In this study 40 children (female: 22, male: 18) were divided into two groups randomly. (20 patients in each group).There were no significant differences at baselines between groups with regard to gender, age and weigh. At the end of the study, the reduction of more than one grade of goiter was significant between iron-treated and placebo groups. In treatment group, 16 patients (80%) had decreased grade of goiter, while in the control group, 3 patients (15%) had grade reduction(P-value<0.001). CONCLUSION: At the end of the study, decrease of more than one grade of goiter had significant differences between iron-treated and control groups. |
format | Online Article Text |
id | pubmed-4173026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Shahid Sadoughi University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-41730262014-09-24 The effect of iron supplement on children with euthyroid goiter: a randomized placebo-controlled clinical trial Ordooei, M Akbarzadeh, M Soleimanizad, R Shamsi, F Masoumi Dehshiri, R Iran J Ped Hematol Oncol Original Article BACKGROUND: Endemic goiter is present in most parts of Iran. Iron deficiency adversely affects the physiology of thyroid. The initial steps of thyroid hormone synthesis are catalyzed by thyroperoxidases and are dependent on iron. In many developing countries, children are at high risk of both goiter and iron deficiency anemia. In addition, iron deficiency may alter central nervous system control of thyroid metabolism; andalso Iron-deficiency anemia decreases plasma concentrations of thyroxine and triiodothyronine. MATERIAL AND METHOD: We conducted a randomized, double-blind,controlled trial in 2-12-y-old children with euthyroid goiter and without iron-deficiency anemia. The children weredivided into two groups: The Patients who were under treatment with ferrous-sulphat and controls .active treatment consisted of iron supplementation was administered orally with a dose of 2 mg/kg day. The duration of active treatment was 12 weeks. RESULTS: In this study 40 children (female: 22, male: 18) were divided into two groups randomly. (20 patients in each group).There were no significant differences at baselines between groups with regard to gender, age and weigh. At the end of the study, the reduction of more than one grade of goiter was significant between iron-treated and placebo groups. In treatment group, 16 patients (80%) had decreased grade of goiter, while in the control group, 3 patients (15%) had grade reduction(P-value<0.001). CONCLUSION: At the end of the study, decrease of more than one grade of goiter had significant differences between iron-treated and control groups. Shahid Sadoughi University of Medical Sciences 2014 2014-07-20 /pmc/articles/PMC4173026/ /pubmed/25254085 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ordooei, M Akbarzadeh, M Soleimanizad, R Shamsi, F Masoumi Dehshiri, R The effect of iron supplement on children with euthyroid goiter: a randomized placebo-controlled clinical trial |
title | The effect of iron supplement on children with euthyroid goiter: a randomized placebo-controlled clinical trial |
title_full | The effect of iron supplement on children with euthyroid goiter: a randomized placebo-controlled clinical trial |
title_fullStr | The effect of iron supplement on children with euthyroid goiter: a randomized placebo-controlled clinical trial |
title_full_unstemmed | The effect of iron supplement on children with euthyroid goiter: a randomized placebo-controlled clinical trial |
title_short | The effect of iron supplement on children with euthyroid goiter: a randomized placebo-controlled clinical trial |
title_sort | effect of iron supplement on children with euthyroid goiter: a randomized placebo-controlled clinical trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173026/ https://www.ncbi.nlm.nih.gov/pubmed/25254085 |
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