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Primary Hypothyroidism and Alzheimer’s Disease: A Tale of Two
Hypothyroidism (HPT) HPT could be a risk factor for the development and progression of Alzheimer’s disease (AD). In addition, progressive neurodegeneration in AD may affect the metabolism of thyroid hormones (THs) in the brain causing local brain HPT. Hence, the present review aimed to clarify the p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477255/ https://www.ncbi.nlm.nih.gov/pubmed/37540395 http://dx.doi.org/10.1007/s10571-023-01392-y |
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author | AlAnazi, Faisal Holil Al-kuraishy, Hayder M. Alexiou, Athanasios Papadakis, Marios Ashour, Mohamed H. Mazhar Alnaaim, Saud A. Elhussieny, Omnya Saad, Hebatallah M. Batiha, Gaber El-Saber |
author_facet | AlAnazi, Faisal Holil Al-kuraishy, Hayder M. Alexiou, Athanasios Papadakis, Marios Ashour, Mohamed H. Mazhar Alnaaim, Saud A. Elhussieny, Omnya Saad, Hebatallah M. Batiha, Gaber El-Saber |
author_sort | AlAnazi, Faisal Holil |
collection | PubMed |
description | Hypothyroidism (HPT) HPT could be a risk factor for the development and progression of Alzheimer’s disease (AD). In addition, progressive neurodegeneration in AD may affect the metabolism of thyroid hormones (THs) in the brain causing local brain HPT. Hence, the present review aimed to clarify the potential association between HPT and AD. HPT promotes the progression of AD by inducing the production of amyloid beta (Aβ) and tau protein phosphorylation with the development of synaptic plasticity and memory dysfunction. Besides, the metabolism of THs is dysregulated in AD due to the accumulation of Aβ and tau protein phosphorylation leading to local brain HPT. Additionally, HPT can affect AD neuropathology through various mechanistic pathways including dysregulation of transthyretin, oxidative stress, ER stress, autophagy dysfunction mitochondrial dysfunction, and inhibition of brain-derived neurotrophic factor. Taken together there is a potential link between HPT and AD, as HPT adversely impacts AD neuropathology and the reverse is also true. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-10477255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-104772552023-09-06 Primary Hypothyroidism and Alzheimer’s Disease: A Tale of Two AlAnazi, Faisal Holil Al-kuraishy, Hayder M. Alexiou, Athanasios Papadakis, Marios Ashour, Mohamed H. Mazhar Alnaaim, Saud A. Elhussieny, Omnya Saad, Hebatallah M. Batiha, Gaber El-Saber Cell Mol Neurobiol Review Paper Hypothyroidism (HPT) HPT could be a risk factor for the development and progression of Alzheimer’s disease (AD). In addition, progressive neurodegeneration in AD may affect the metabolism of thyroid hormones (THs) in the brain causing local brain HPT. Hence, the present review aimed to clarify the potential association between HPT and AD. HPT promotes the progression of AD by inducing the production of amyloid beta (Aβ) and tau protein phosphorylation with the development of synaptic plasticity and memory dysfunction. Besides, the metabolism of THs is dysregulated in AD due to the accumulation of Aβ and tau protein phosphorylation leading to local brain HPT. Additionally, HPT can affect AD neuropathology through various mechanistic pathways including dysregulation of transthyretin, oxidative stress, ER stress, autophagy dysfunction mitochondrial dysfunction, and inhibition of brain-derived neurotrophic factor. Taken together there is a potential link between HPT and AD, as HPT adversely impacts AD neuropathology and the reverse is also true. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2023-08-04 2023 /pmc/articles/PMC10477255/ /pubmed/37540395 http://dx.doi.org/10.1007/s10571-023-01392-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Paper AlAnazi, Faisal Holil Al-kuraishy, Hayder M. Alexiou, Athanasios Papadakis, Marios Ashour, Mohamed H. Mazhar Alnaaim, Saud A. Elhussieny, Omnya Saad, Hebatallah M. Batiha, Gaber El-Saber Primary Hypothyroidism and Alzheimer’s Disease: A Tale of Two |
title | Primary Hypothyroidism and Alzheimer’s Disease: A Tale of Two |
title_full | Primary Hypothyroidism and Alzheimer’s Disease: A Tale of Two |
title_fullStr | Primary Hypothyroidism and Alzheimer’s Disease: A Tale of Two |
title_full_unstemmed | Primary Hypothyroidism and Alzheimer’s Disease: A Tale of Two |
title_short | Primary Hypothyroidism and Alzheimer’s Disease: A Tale of Two |
title_sort | primary hypothyroidism and alzheimer’s disease: a tale of two |
topic | Review Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477255/ https://www.ncbi.nlm.nih.gov/pubmed/37540395 http://dx.doi.org/10.1007/s10571-023-01392-y |
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