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Neuropsychiatric Disturbances in Alzheimer’s Disease: What Have We Learned from Neuropathological Studies?
Neuropsychiatric symptoms (NPS) are an integral part of the dementia syndrome and were therefore recently included in the core diagnostic criteria of dementia. The near universal prevalence of NPS in Alzheimer’s disease (AD), combined with their disabling effects on patients and caregivers, is contr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070416/ https://www.ncbi.nlm.nih.gov/pubmed/27137218 http://dx.doi.org/10.2174/1567205013666160502123607 |
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author | Van Dam, Debby Vermeiren, Yannick Dekker, Alain D. Naudé, Petrus J.W. De Deyn, Peter P. |
author_facet | Van Dam, Debby Vermeiren, Yannick Dekker, Alain D. Naudé, Petrus J.W. De Deyn, Peter P. |
author_sort | Van Dam, Debby |
collection | PubMed |
description | Neuropsychiatric symptoms (NPS) are an integral part of the dementia syndrome and were therefore recently included in the core diagnostic criteria of dementia. The near universal prevalence of NPS in Alzheimer’s disease (AD), combined with their disabling effects on patients and caregivers, is contrasted by the fact that few effective and safe treatments exist, which is in part to be attributed to our incomplete understanding of the neurobiology of NPS. In this review, we describe the pathological alterations typical for AD, including spreading and evolution of burden, effect on the molecular and cellular integrity, functional consequences and atrophy of NPS-relevant brain regions and circuits in correlation with specific NPS assessments. It is thereby clearly established that NPS are fundamental expressions of the underlying neurodegenerative brain disease and not simply reflect the patients’ secondary response to their illness. Neuropathological studies, moreover, include a majority of end-stage patient samples, which may not correctly represent the pathophysiological environment responsible for particular NPS that may already be present in an early stage, or even prior to AD diagnosis. The burdensome nature and high prevalence of NPS, in combination with the absence of effective and safe pharmacotherapies, provide a strong incentive to continue neuropathological and neurochemical, as well as imaging and other relevant approaches to further improve our apprehension of the neurobiology of NPS. |
format | Online Article Text |
id | pubmed-5070416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-50704162016-11-14 Neuropsychiatric Disturbances in Alzheimer’s Disease: What Have We Learned from Neuropathological Studies? Van Dam, Debby Vermeiren, Yannick Dekker, Alain D. Naudé, Petrus J.W. De Deyn, Peter P. Curr Alzheimer Res Article Neuropsychiatric symptoms (NPS) are an integral part of the dementia syndrome and were therefore recently included in the core diagnostic criteria of dementia. The near universal prevalence of NPS in Alzheimer’s disease (AD), combined with their disabling effects on patients and caregivers, is contrasted by the fact that few effective and safe treatments exist, which is in part to be attributed to our incomplete understanding of the neurobiology of NPS. In this review, we describe the pathological alterations typical for AD, including spreading and evolution of burden, effect on the molecular and cellular integrity, functional consequences and atrophy of NPS-relevant brain regions and circuits in correlation with specific NPS assessments. It is thereby clearly established that NPS are fundamental expressions of the underlying neurodegenerative brain disease and not simply reflect the patients’ secondary response to their illness. Neuropathological studies, moreover, include a majority of end-stage patient samples, which may not correctly represent the pathophysiological environment responsible for particular NPS that may already be present in an early stage, or even prior to AD diagnosis. The burdensome nature and high prevalence of NPS, in combination with the absence of effective and safe pharmacotherapies, provide a strong incentive to continue neuropathological and neurochemical, as well as imaging and other relevant approaches to further improve our apprehension of the neurobiology of NPS. Bentham Science Publishers 2016-10 2016-10 /pmc/articles/PMC5070416/ /pubmed/27137218 http://dx.doi.org/10.2174/1567205013666160502123607 Text en © 2016 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) ( https://creativecommons.org/licenses/by-nc/4.0/legalcode ), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Van Dam, Debby Vermeiren, Yannick Dekker, Alain D. Naudé, Petrus J.W. De Deyn, Peter P. Neuropsychiatric Disturbances in Alzheimer’s Disease: What Have We Learned from Neuropathological Studies? |
title | Neuropsychiatric Disturbances in Alzheimer’s Disease: What Have We Learned from Neuropathological Studies? |
title_full | Neuropsychiatric Disturbances in Alzheimer’s Disease: What Have We Learned from Neuropathological Studies? |
title_fullStr | Neuropsychiatric Disturbances in Alzheimer’s Disease: What Have We Learned from Neuropathological Studies? |
title_full_unstemmed | Neuropsychiatric Disturbances in Alzheimer’s Disease: What Have We Learned from Neuropathological Studies? |
title_short | Neuropsychiatric Disturbances in Alzheimer’s Disease: What Have We Learned from Neuropathological Studies? |
title_sort | neuropsychiatric disturbances in alzheimer’s disease: what have we learned from neuropathological studies? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070416/ https://www.ncbi.nlm.nih.gov/pubmed/27137218 http://dx.doi.org/10.2174/1567205013666160502123607 |
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