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Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease

The major product secreted by the thyroid is thyroxine (T4), whereas most of the biologically active triiodothyronine (T3) derives from the peripheral conversion of T4 into T3. The deiodinase enzymes are involved in activation and inactivation of thyroid hormones (THs). Type 1 and type 2 deiodinase...

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Autores principales: Luongo, Cristina, Trivisano, Luigi, Alfano, Fausta, Salvatore, Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3761349/
https://www.ncbi.nlm.nih.gov/pubmed/24027558
http://dx.doi.org/10.3389/fendo.2013.00115
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author Luongo, Cristina
Trivisano, Luigi
Alfano, Fausta
Salvatore, Domenico
author_facet Luongo, Cristina
Trivisano, Luigi
Alfano, Fausta
Salvatore, Domenico
author_sort Luongo, Cristina
collection PubMed
description The major product secreted by the thyroid is thyroxine (T4), whereas most of the biologically active triiodothyronine (T3) derives from the peripheral conversion of T4 into T3. The deiodinase enzymes are involved in activation and inactivation of thyroid hormones (THs). Type 1 and type 2 deiodinase (D1 and D2) convert T4 into T3 whereas D3 degrades T4 and T3 into inactive metabolites and is thus the major physiological TH inactivator. The hypothalamic-pituitary-thyroid axis maintains circulating TH levels constant, while the deiodinases tissue-specifically regulate intracellular thyroid status by controlling TH action in a precise spatio-temporal fashion. Here we review the data related to the recent identification of a paraneoplastic syndrome called “consumptive hypothyroidism,” which exemplifies how deiodinases alter substantially the concentration of TH in blood. This syndrome results from the aberrant uncontrolled expression of D3 that can induce a severe form of hypothyroidism by inactivating T4 and T3 in defined tumor tissue. This rare TH insufficiency generally affects patients in the first years of life, and has distinct features in terms of diagnosis, treatment, and prognosis with respect to other forms of hypothyroidism.
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spelling pubmed-37613492013-09-11 Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease Luongo, Cristina Trivisano, Luigi Alfano, Fausta Salvatore, Domenico Front Endocrinol (Lausanne) Endocrinology The major product secreted by the thyroid is thyroxine (T4), whereas most of the biologically active triiodothyronine (T3) derives from the peripheral conversion of T4 into T3. The deiodinase enzymes are involved in activation and inactivation of thyroid hormones (THs). Type 1 and type 2 deiodinase (D1 and D2) convert T4 into T3 whereas D3 degrades T4 and T3 into inactive metabolites and is thus the major physiological TH inactivator. The hypothalamic-pituitary-thyroid axis maintains circulating TH levels constant, while the deiodinases tissue-specifically regulate intracellular thyroid status by controlling TH action in a precise spatio-temporal fashion. Here we review the data related to the recent identification of a paraneoplastic syndrome called “consumptive hypothyroidism,” which exemplifies how deiodinases alter substantially the concentration of TH in blood. This syndrome results from the aberrant uncontrolled expression of D3 that can induce a severe form of hypothyroidism by inactivating T4 and T3 in defined tumor tissue. This rare TH insufficiency generally affects patients in the first years of life, and has distinct features in terms of diagnosis, treatment, and prognosis with respect to other forms of hypothyroidism. Frontiers Media S.A. 2013-09-04 /pmc/articles/PMC3761349/ /pubmed/24027558 http://dx.doi.org/10.3389/fendo.2013.00115 Text en Copyright © 2013 Luongo, Trivisano, Alfano and Salvatore. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Luongo, Cristina
Trivisano, Luigi
Alfano, Fausta
Salvatore, Domenico
Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease
title Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease
title_full Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease
title_fullStr Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease
title_full_unstemmed Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease
title_short Type 3 Deiodinase and Consumptive Hypothyroidism: A Common Mechanism for a Rare Disease
title_sort type 3 deiodinase and consumptive hypothyroidism: a common mechanism for a rare disease
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3761349/
https://www.ncbi.nlm.nih.gov/pubmed/24027558
http://dx.doi.org/10.3389/fendo.2013.00115
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