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The role of thyroid hormone in metabolism and metabolic syndrome

Metabolic syndrome (MetS) and thyroid dysfunction are common in clinical practice. The objectives of this review are to discuss some proposed mechanisms by which thyroid dysfunctions may lead to MetS, to describe the bidirectional relationship between thyroid hormones (THs) and adiposity and finally...

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Autores principales: Teixeira, Patrícia de Fátima dos Santos, dos Santos, Patrícia Borges, Pazos-Moura, Carmen Cabanelas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238803/
https://www.ncbi.nlm.nih.gov/pubmed/32489580
http://dx.doi.org/10.1177/2042018820917869
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author Teixeira, Patrícia de Fátima dos Santos
dos Santos, Patrícia Borges
Pazos-Moura, Carmen Cabanelas
author_facet Teixeira, Patrícia de Fátima dos Santos
dos Santos, Patrícia Borges
Pazos-Moura, Carmen Cabanelas
author_sort Teixeira, Patrícia de Fátima dos Santos
collection PubMed
description Metabolic syndrome (MetS) and thyroid dysfunction are common in clinical practice. The objectives of this review are to discuss some proposed mechanisms by which thyroid dysfunctions may lead to MetS, to describe the bidirectional relationship between thyroid hormones (THs) and adiposity and finally, to resume a list of recent studies in humans that evaluated possible associations between thyroid hormone status and MetS or its clinical components. Not solely THs, but also its metabolites regulate metabolic rate, influencing adiposity. The mechanisms enrolled are related to its direct effect on adenosine triphosphate (ATP) utilization, uncoupling synthesis of ATP, mitochondrial biogenesis, and its inotropic and chronotropic effects. THs also act controlling core body temperature, appetite, and sympathetic activity. In a bidirectional way, thyroid function is affected by adiposity. Leptin is one of the hallmarks, but the pro-inflammatory cytokines and also insulin resistance impact thyroid function and perhaps its structure. MetS development and weight gain have been positively associated with thyroid-stimulating hormone (TSH) in several studies. Adverse glucose metabolism may be related to hyperthyroidism, but also to reduction of thyroid function or higher serum TSH, as do abnormal serum triglyceride levels. Hypo- and hyperthyroidism have been related to higher blood pressure (BP), that may be consequence of genomic or nongenomic action of THs on the vasculature and in the heart. In summary, the interaction between THs and components of MetS is complex and not fully understood. More longitudinal studies controlling each of all confounding variables that interact with endpoints or exposure factors are still necessary.
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spelling pubmed-72388032020-06-01 The role of thyroid hormone in metabolism and metabolic syndrome Teixeira, Patrícia de Fátima dos Santos dos Santos, Patrícia Borges Pazos-Moura, Carmen Cabanelas Ther Adv Endocrinol Metab Obesity Complications: Challenges and Clinical Impact Metabolic syndrome (MetS) and thyroid dysfunction are common in clinical practice. The objectives of this review are to discuss some proposed mechanisms by which thyroid dysfunctions may lead to MetS, to describe the bidirectional relationship between thyroid hormones (THs) and adiposity and finally, to resume a list of recent studies in humans that evaluated possible associations between thyroid hormone status and MetS or its clinical components. Not solely THs, but also its metabolites regulate metabolic rate, influencing adiposity. The mechanisms enrolled are related to its direct effect on adenosine triphosphate (ATP) utilization, uncoupling synthesis of ATP, mitochondrial biogenesis, and its inotropic and chronotropic effects. THs also act controlling core body temperature, appetite, and sympathetic activity. In a bidirectional way, thyroid function is affected by adiposity. Leptin is one of the hallmarks, but the pro-inflammatory cytokines and also insulin resistance impact thyroid function and perhaps its structure. MetS development and weight gain have been positively associated with thyroid-stimulating hormone (TSH) in several studies. Adverse glucose metabolism may be related to hyperthyroidism, but also to reduction of thyroid function or higher serum TSH, as do abnormal serum triglyceride levels. Hypo- and hyperthyroidism have been related to higher blood pressure (BP), that may be consequence of genomic or nongenomic action of THs on the vasculature and in the heart. In summary, the interaction between THs and components of MetS is complex and not fully understood. More longitudinal studies controlling each of all confounding variables that interact with endpoints or exposure factors are still necessary. SAGE Publications 2020-05-13 /pmc/articles/PMC7238803/ /pubmed/32489580 http://dx.doi.org/10.1177/2042018820917869 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Obesity Complications: Challenges and Clinical Impact
Teixeira, Patrícia de Fátima dos Santos
dos Santos, Patrícia Borges
Pazos-Moura, Carmen Cabanelas
The role of thyroid hormone in metabolism and metabolic syndrome
title The role of thyroid hormone in metabolism and metabolic syndrome
title_full The role of thyroid hormone in metabolism and metabolic syndrome
title_fullStr The role of thyroid hormone in metabolism and metabolic syndrome
title_full_unstemmed The role of thyroid hormone in metabolism and metabolic syndrome
title_short The role of thyroid hormone in metabolism and metabolic syndrome
title_sort role of thyroid hormone in metabolism and metabolic syndrome
topic Obesity Complications: Challenges and Clinical Impact
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238803/
https://www.ncbi.nlm.nih.gov/pubmed/32489580
http://dx.doi.org/10.1177/2042018820917869
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