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A 10‐year prevalence of congenital hypothyroidism in Khorramabad (Urban Western Iran)

BACKGROUND: Congenital hypothyroidism in infants is the cause of mental retardation in children, it can be detected in patient and treated at a relatively cheap rate, preventing patient retard. This study aimed to determine the prevalence of congenital hypothyroidism among Khorramabad children. METH...

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Autores principales: Taee, Nadereh, Faraji Goodarzi, Mojgan, Safdari, Mohammad, Bajelan, Amir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687863/
https://www.ncbi.nlm.nih.gov/pubmed/31215165
http://dx.doi.org/10.1002/mgg3.817
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author Taee, Nadereh
Faraji Goodarzi, Mojgan
Safdari, Mohammad
Bajelan, Amir
author_facet Taee, Nadereh
Faraji Goodarzi, Mojgan
Safdari, Mohammad
Bajelan, Amir
author_sort Taee, Nadereh
collection PubMed
description BACKGROUND: Congenital hypothyroidism in infants is the cause of mental retardation in children, it can be detected in patient and treated at a relatively cheap rate, preventing patient retard. This study aimed to determine the prevalence of congenital hypothyroidism among Khorramabad children. METHODS: In the present study, we identified all patients who had received levothyroxine prescriptions during the study period (2007–2017). Using this as a congenital hypothyroidism surrogate marker, we considered the congenital hypothyroidism prevalence in children above 3 years. RESULTS: Of 574 patients who had received levothyroxine during the neonatal period up to 3 years, the results of one‐variable logistic regression analysis showed that the chance of temporary disease in children with small thyroid ultrasonography was 62% less, than for those without problems, and this difference was significant. The chance of temporary disease in children who had other cases was 87% less than those without problems, and this difference was statistically significant. CONCLUSION: The overall prevalence of congenital hypothyroidism in young patients up to 3 years is 0.143%, these values are at least twice those of previous estimates. This proposes an elevation in autoimmune thyroid disease, which is similitude to the rising prevalence of diabetes type 1, which possibly indicates a rising incidence of autoimmunity in youth.
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spelling pubmed-66878632019-08-14 A 10‐year prevalence of congenital hypothyroidism in Khorramabad (Urban Western Iran) Taee, Nadereh Faraji Goodarzi, Mojgan Safdari, Mohammad Bajelan, Amir Mol Genet Genomic Med Original Articles BACKGROUND: Congenital hypothyroidism in infants is the cause of mental retardation in children, it can be detected in patient and treated at a relatively cheap rate, preventing patient retard. This study aimed to determine the prevalence of congenital hypothyroidism among Khorramabad children. METHODS: In the present study, we identified all patients who had received levothyroxine prescriptions during the study period (2007–2017). Using this as a congenital hypothyroidism surrogate marker, we considered the congenital hypothyroidism prevalence in children above 3 years. RESULTS: Of 574 patients who had received levothyroxine during the neonatal period up to 3 years, the results of one‐variable logistic regression analysis showed that the chance of temporary disease in children with small thyroid ultrasonography was 62% less, than for those without problems, and this difference was significant. The chance of temporary disease in children who had other cases was 87% less than those without problems, and this difference was statistically significant. CONCLUSION: The overall prevalence of congenital hypothyroidism in young patients up to 3 years is 0.143%, these values are at least twice those of previous estimates. This proposes an elevation in autoimmune thyroid disease, which is similitude to the rising prevalence of diabetes type 1, which possibly indicates a rising incidence of autoimmunity in youth. John Wiley and Sons Inc. 2019-06-18 /pmc/articles/PMC6687863/ /pubmed/31215165 http://dx.doi.org/10.1002/mgg3.817 Text en © 2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Taee, Nadereh
Faraji Goodarzi, Mojgan
Safdari, Mohammad
Bajelan, Amir
A 10‐year prevalence of congenital hypothyroidism in Khorramabad (Urban Western Iran)
title A 10‐year prevalence of congenital hypothyroidism in Khorramabad (Urban Western Iran)
title_full A 10‐year prevalence of congenital hypothyroidism in Khorramabad (Urban Western Iran)
title_fullStr A 10‐year prevalence of congenital hypothyroidism in Khorramabad (Urban Western Iran)
title_full_unstemmed A 10‐year prevalence of congenital hypothyroidism in Khorramabad (Urban Western Iran)
title_short A 10‐year prevalence of congenital hypothyroidism in Khorramabad (Urban Western Iran)
title_sort 10‐year prevalence of congenital hypothyroidism in khorramabad (urban western iran)
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687863/
https://www.ncbi.nlm.nih.gov/pubmed/31215165
http://dx.doi.org/10.1002/mgg3.817
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