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Alzheimer’s Disease and Impaired Bone Microarchitecture, Regeneration and Potential Genetic Links
Alzheimer’s Disease (AD) and osteoporosis are both age-related degenerative diseases. Many studies indicate that these two diseases share common pathogenesis mechanisms. In this review, the osteoporotic phenotype of AD mouse models was discussed, and shared mechanisms such as hormonal imbalance, gen...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963274/ https://www.ncbi.nlm.nih.gov/pubmed/36836731 http://dx.doi.org/10.3390/life13020373 |
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author | Zhang, Min Hu, Shunze Sun, Xuying |
author_facet | Zhang, Min Hu, Shunze Sun, Xuying |
author_sort | Zhang, Min |
collection | PubMed |
description | Alzheimer’s Disease (AD) and osteoporosis are both age-related degenerative diseases. Many studies indicate that these two diseases share common pathogenesis mechanisms. In this review, the osteoporotic phenotype of AD mouse models was discussed, and shared mechanisms such as hormonal imbalance, genetic factors, similar signaling pathways and impaired neurotransmitters were identified. Moreover, the review provides recent data associated with these two diseases. Furthermore, potential therapeutic approaches targeting both diseases were discussed. Thus, we proposed that preventing bone loss should be one of the most important treatment goals in patients with AD; treatment targeting brain disorders is also beneficial for osteoporosis. |
format | Online Article Text |
id | pubmed-9963274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99632742023-02-26 Alzheimer’s Disease and Impaired Bone Microarchitecture, Regeneration and Potential Genetic Links Zhang, Min Hu, Shunze Sun, Xuying Life (Basel) Review Alzheimer’s Disease (AD) and osteoporosis are both age-related degenerative diseases. Many studies indicate that these two diseases share common pathogenesis mechanisms. In this review, the osteoporotic phenotype of AD mouse models was discussed, and shared mechanisms such as hormonal imbalance, genetic factors, similar signaling pathways and impaired neurotransmitters were identified. Moreover, the review provides recent data associated with these two diseases. Furthermore, potential therapeutic approaches targeting both diseases were discussed. Thus, we proposed that preventing bone loss should be one of the most important treatment goals in patients with AD; treatment targeting brain disorders is also beneficial for osteoporosis. MDPI 2023-01-29 /pmc/articles/PMC9963274/ /pubmed/36836731 http://dx.doi.org/10.3390/life13020373 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Zhang, Min Hu, Shunze Sun, Xuying Alzheimer’s Disease and Impaired Bone Microarchitecture, Regeneration and Potential Genetic Links |
title | Alzheimer’s Disease and Impaired Bone Microarchitecture, Regeneration and Potential Genetic Links |
title_full | Alzheimer’s Disease and Impaired Bone Microarchitecture, Regeneration and Potential Genetic Links |
title_fullStr | Alzheimer’s Disease and Impaired Bone Microarchitecture, Regeneration and Potential Genetic Links |
title_full_unstemmed | Alzheimer’s Disease and Impaired Bone Microarchitecture, Regeneration and Potential Genetic Links |
title_short | Alzheimer’s Disease and Impaired Bone Microarchitecture, Regeneration and Potential Genetic Links |
title_sort | alzheimer’s disease and impaired bone microarchitecture, regeneration and potential genetic links |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963274/ https://www.ncbi.nlm.nih.gov/pubmed/36836731 http://dx.doi.org/10.3390/life13020373 |
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