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Risk factors for short term thyroid dysfunction after hematopoietic stem cell transplantation in children

PURPOSE: The purpose of this study was to evaluate short-term thyroid dysfunction and related risk factors in pediatric patients who underwent hematopoietic stem cell transplantation (HSCT) during childhood. METHODS: We studied 166 patients (100 boys and 66 girls) who underwent HSCT at the Catholic...

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Autores principales: Jung, You Jin, Jeon, Yeon Jin, Cho, Won Kyoung, Lee, Jae Wook, Chung, Nack-Gyun, Jung, Min Ho, Cho, Bin, Suh, Byung-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728449/
https://www.ncbi.nlm.nih.gov/pubmed/23908670
http://dx.doi.org/10.3345/kjp.2013.56.7.298
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author Jung, You Jin
Jeon, Yeon Jin
Cho, Won Kyoung
Lee, Jae Wook
Chung, Nack-Gyun
Jung, Min Ho
Cho, Bin
Suh, Byung-Kyu
author_facet Jung, You Jin
Jeon, Yeon Jin
Cho, Won Kyoung
Lee, Jae Wook
Chung, Nack-Gyun
Jung, Min Ho
Cho, Bin
Suh, Byung-Kyu
author_sort Jung, You Jin
collection PubMed
description PURPOSE: The purpose of this study was to evaluate short-term thyroid dysfunction and related risk factors in pediatric patients who underwent hematopoietic stem cell transplantation (HSCT) during childhood. METHODS: We studied 166 patients (100 boys and 66 girls) who underwent HSCT at the Catholic HSCT Center from January 2004 through December 2009. The mean age at HSCT was 10.0±4.8 years. Thyroid function of the patients was tested before and during 3 months of HSCT. RESULTS: Out of 166 patients, 165 (99.4%) underwent allotransplantation. Acute graft-versus-host disease (GVHD, grades II to IV) developed in 76 patients. Conditioning regimens before HSCT include total body irradiation (n=57), busulfan (n=80), and reduced intensity (n=29). Forty-five (27.1%) had thyroid dysfunction during 3 months after HSCT (29 euthyroid sick syndrome [ESS], 6 subclinical hyperthyroidism, 4 subclinical hypothyroidism, 3 hypothyroxinemia, 2 overt hyperthyroidism, and 1 high T(4) syndrome). In a univariate logistic regression analysis, age at HSCT (P=0.002) and acute GVHD (P=0.009) had statistically significant relationships with thyroid dysfunction during 3 months after HSCT. Also, in a univariate logistic regression analysis, ESS (P=0.014) showed a strong statistically significant association with mortality. CONCLUSION: In our study 27.1% patients experienced thyroid dysfunction during 3 months after HSCT. Increase in age and acute GVHD may be risk factors for thyroid dysfunction during 3 months after HSCT. There was a significant association between ESS and mortality.
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spelling pubmed-37284492013-08-01 Risk factors for short term thyroid dysfunction after hematopoietic stem cell transplantation in children Jung, You Jin Jeon, Yeon Jin Cho, Won Kyoung Lee, Jae Wook Chung, Nack-Gyun Jung, Min Ho Cho, Bin Suh, Byung-Kyu Korean J Pediatr Original Article PURPOSE: The purpose of this study was to evaluate short-term thyroid dysfunction and related risk factors in pediatric patients who underwent hematopoietic stem cell transplantation (HSCT) during childhood. METHODS: We studied 166 patients (100 boys and 66 girls) who underwent HSCT at the Catholic HSCT Center from January 2004 through December 2009. The mean age at HSCT was 10.0±4.8 years. Thyroid function of the patients was tested before and during 3 months of HSCT. RESULTS: Out of 166 patients, 165 (99.4%) underwent allotransplantation. Acute graft-versus-host disease (GVHD, grades II to IV) developed in 76 patients. Conditioning regimens before HSCT include total body irradiation (n=57), busulfan (n=80), and reduced intensity (n=29). Forty-five (27.1%) had thyroid dysfunction during 3 months after HSCT (29 euthyroid sick syndrome [ESS], 6 subclinical hyperthyroidism, 4 subclinical hypothyroidism, 3 hypothyroxinemia, 2 overt hyperthyroidism, and 1 high T(4) syndrome). In a univariate logistic regression analysis, age at HSCT (P=0.002) and acute GVHD (P=0.009) had statistically significant relationships with thyroid dysfunction during 3 months after HSCT. Also, in a univariate logistic regression analysis, ESS (P=0.014) showed a strong statistically significant association with mortality. CONCLUSION: In our study 27.1% patients experienced thyroid dysfunction during 3 months after HSCT. Increase in age and acute GVHD may be risk factors for thyroid dysfunction during 3 months after HSCT. There was a significant association between ESS and mortality. The Korean Pediatric Society 2013-07 2013-07-19 /pmc/articles/PMC3728449/ /pubmed/23908670 http://dx.doi.org/10.3345/kjp.2013.56.7.298 Text en Copyright © 2013 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jung, You Jin
Jeon, Yeon Jin
Cho, Won Kyoung
Lee, Jae Wook
Chung, Nack-Gyun
Jung, Min Ho
Cho, Bin
Suh, Byung-Kyu
Risk factors for short term thyroid dysfunction after hematopoietic stem cell transplantation in children
title Risk factors for short term thyroid dysfunction after hematopoietic stem cell transplantation in children
title_full Risk factors for short term thyroid dysfunction after hematopoietic stem cell transplantation in children
title_fullStr Risk factors for short term thyroid dysfunction after hematopoietic stem cell transplantation in children
title_full_unstemmed Risk factors for short term thyroid dysfunction after hematopoietic stem cell transplantation in children
title_short Risk factors for short term thyroid dysfunction after hematopoietic stem cell transplantation in children
title_sort risk factors for short term thyroid dysfunction after hematopoietic stem cell transplantation in children
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728449/
https://www.ncbi.nlm.nih.gov/pubmed/23908670
http://dx.doi.org/10.3345/kjp.2013.56.7.298
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