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Functional correlates of TSH, fT3 and fT4 in Alzheimer disease: a F-18 FDG PET/CT study

The present study was aimed to investigate the relationships between thyroid stimulating hormone (TSH), freeT3 (fT3) and freeT4 (fT4) and brain glucose consumption as detectable by means of 2-deoxy-2-(F-18) fluoro-D-glucose (F-18 FDG) Positron Emission Tomography/Computed Tomography (PET/CT) in a se...

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Autores principales: Chiaravalloti, Agostino, Ursini, Francesco, Fiorentini, Alessandro, Barbagallo, Gaetano, Martorana, Alessandro, Koch, Giacomo, Tavolozza, Mario, Schillaci, Orazio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524843/
https://www.ncbi.nlm.nih.gov/pubmed/28740088
http://dx.doi.org/10.1038/s41598-017-06138-7
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author Chiaravalloti, Agostino
Ursini, Francesco
Fiorentini, Alessandro
Barbagallo, Gaetano
Martorana, Alessandro
Koch, Giacomo
Tavolozza, Mario
Schillaci, Orazio
author_facet Chiaravalloti, Agostino
Ursini, Francesco
Fiorentini, Alessandro
Barbagallo, Gaetano
Martorana, Alessandro
Koch, Giacomo
Tavolozza, Mario
Schillaci, Orazio
author_sort Chiaravalloti, Agostino
collection PubMed
description The present study was aimed to investigate the relationships between thyroid stimulating hormone (TSH), freeT3 (fT3) and freeT4 (fT4) and brain glucose consumption as detectable by means of 2-deoxy-2-(F-18) fluoro-D-glucose (F-18 FDG) Positron Emission Tomography/Computed Tomography (PET/CT) in a selected population with Alzheimer disease (AD). We evaluated 87 subjects (37 males and 50 females, mean age 70 (±6) years old) with AD. All of them were subjected to TSH, fT3 and fT4 assay and to cerebrospinal fluid amyloid (Aβ1-42) and tau [phosphorylated-tau (p-tau) and total-tau (t-tau)] assay prior PET/CT examination. Values for TSH, fT3 and fT4 were in the normal range. The relationships were evaluated by means of statistical parametric mapping (SPM8) using age, sex, MMSE, scholarship and CSF values of amyloid and tau as covariates. We found a significant positive correlation between TSH values and cortical glucose consumption in a wide portion of the anterior cingulate cortex bilaterally (BA32) and left frontal lobe (BA25) (p FWE-corr <0.001; p FDRcorr <0.000; cluster extent 66950). No significant relationships were found between cortical F-18 FDG uptake and T3 and T4 serum levels. The results of our study suggest that a cortical dysfunction in anterior cingulate and frontal lobes may affect serum values of TSH in AD patients.
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spelling pubmed-55248432017-07-26 Functional correlates of TSH, fT3 and fT4 in Alzheimer disease: a F-18 FDG PET/CT study Chiaravalloti, Agostino Ursini, Francesco Fiorentini, Alessandro Barbagallo, Gaetano Martorana, Alessandro Koch, Giacomo Tavolozza, Mario Schillaci, Orazio Sci Rep Article The present study was aimed to investigate the relationships between thyroid stimulating hormone (TSH), freeT3 (fT3) and freeT4 (fT4) and brain glucose consumption as detectable by means of 2-deoxy-2-(F-18) fluoro-D-glucose (F-18 FDG) Positron Emission Tomography/Computed Tomography (PET/CT) in a selected population with Alzheimer disease (AD). We evaluated 87 subjects (37 males and 50 females, mean age 70 (±6) years old) with AD. All of them were subjected to TSH, fT3 and fT4 assay and to cerebrospinal fluid amyloid (Aβ1-42) and tau [phosphorylated-tau (p-tau) and total-tau (t-tau)] assay prior PET/CT examination. Values for TSH, fT3 and fT4 were in the normal range. The relationships were evaluated by means of statistical parametric mapping (SPM8) using age, sex, MMSE, scholarship and CSF values of amyloid and tau as covariates. We found a significant positive correlation between TSH values and cortical glucose consumption in a wide portion of the anterior cingulate cortex bilaterally (BA32) and left frontal lobe (BA25) (p FWE-corr <0.001; p FDRcorr <0.000; cluster extent 66950). No significant relationships were found between cortical F-18 FDG uptake and T3 and T4 serum levels. The results of our study suggest that a cortical dysfunction in anterior cingulate and frontal lobes may affect serum values of TSH in AD patients. Nature Publishing Group UK 2017-07-24 /pmc/articles/PMC5524843/ /pubmed/28740088 http://dx.doi.org/10.1038/s41598-017-06138-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chiaravalloti, Agostino
Ursini, Francesco
Fiorentini, Alessandro
Barbagallo, Gaetano
Martorana, Alessandro
Koch, Giacomo
Tavolozza, Mario
Schillaci, Orazio
Functional correlates of TSH, fT3 and fT4 in Alzheimer disease: a F-18 FDG PET/CT study
title Functional correlates of TSH, fT3 and fT4 in Alzheimer disease: a F-18 FDG PET/CT study
title_full Functional correlates of TSH, fT3 and fT4 in Alzheimer disease: a F-18 FDG PET/CT study
title_fullStr Functional correlates of TSH, fT3 and fT4 in Alzheimer disease: a F-18 FDG PET/CT study
title_full_unstemmed Functional correlates of TSH, fT3 and fT4 in Alzheimer disease: a F-18 FDG PET/CT study
title_short Functional correlates of TSH, fT3 and fT4 in Alzheimer disease: a F-18 FDG PET/CT study
title_sort functional correlates of tsh, ft3 and ft4 in alzheimer disease: a f-18 fdg pet/ct study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524843/
https://www.ncbi.nlm.nih.gov/pubmed/28740088
http://dx.doi.org/10.1038/s41598-017-06138-7
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