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Involvement of inflammation in the medial temporal region in the development of agitation in Alzheimer's disease: an in vivo positron emission tomography study
BACKGROUND: The evaluation of (11)C‐DPA‐713 binding using positron emission tomography for quantifying the translocator protein can be a sensitive approach in determining the level of glial activation induced by neuroinflammation. Herein, we aimed to investigate the relationship between regional (11...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10100091/ https://www.ncbi.nlm.nih.gov/pubmed/36403981 http://dx.doi.org/10.1111/psyg.12915 |
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author | Yasuno, Fumihiko Kimura, Yasuyuki Ogata, Aya Ikenuma, Hiroshi Abe, Junichiro Minami, Hiroyuki Nihashi, Takashi Yokoi, Kastunori Hattori, Saori Shimoda, Nobuyoshi Watanabe, Atsushi Kasuga, Kensaku Ikeuchi, Takeshi Takeda, Akinori Sakurai, Takashi Ito, Kengo Kato, Takashi |
author_facet | Yasuno, Fumihiko Kimura, Yasuyuki Ogata, Aya Ikenuma, Hiroshi Abe, Junichiro Minami, Hiroyuki Nihashi, Takashi Yokoi, Kastunori Hattori, Saori Shimoda, Nobuyoshi Watanabe, Atsushi Kasuga, Kensaku Ikeuchi, Takeshi Takeda, Akinori Sakurai, Takashi Ito, Kengo Kato, Takashi |
author_sort | Yasuno, Fumihiko |
collection | PubMed |
description | BACKGROUND: The evaluation of (11)C‐DPA‐713 binding using positron emission tomography for quantifying the translocator protein can be a sensitive approach in determining the level of glial activation induced by neuroinflammation. Herein, we aimed to investigate the relationship between regional (11)C‐DPA713‐binding potential (BP(ND)) and neuropsychiatric symptoms (NPS) in amyloid‐positive Alzheimer's disease (AD) patients. METHODS: Fifteen AD patients were enrolled in this study. Correlations were evaluated between the (11)C‐DPA713‐BP(ND) and Neuropsychiatric Inventory Questionnaire (NPI‐Q) scores, including scores in its four domains: agitation, psychosis, affective, and apathy. (11)C‐DPA713‐BP(ND) values were compared between groups with and without the neuropsychiatric symptoms for which a relationship was observed in the abovementioned correlation analysis. RESULTS: A positive correlation was found between the severity of agitation and (11)C‐DPA713‐BP(ND) in the Braak 1–3 area, including the amygdala, hippocampal and parahippocampal regions, and lingual and fusiform areas. An increase in the (11)C‐DPA713‐BP(ND) was observed in AD patients with agitation. We did not find any significant effects of possible confounding factors, such as age, duration of illness, education, gender, Mini‐Mental State Examination score, cerebrospinal fluid amyloid β 42/40 ratio, and apolipoprotein E4 positivity, on either the (11)C‐DPA713‐BP(ND) or agitation score. CONCLUSIONS: Neuroinflammation in the medial temporal region and its neighbouring area was shown to be associated with the development of agitation symptoms in AD patients. Our findings extend those of previous studies showing an association between some NPS and inflammation, suggesting that immunologically based interventions for agitation can serve as an alternative treatment for dementia. |
format | Online Article Text |
id | pubmed-10100091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-101000912023-04-14 Involvement of inflammation in the medial temporal region in the development of agitation in Alzheimer's disease: an in vivo positron emission tomography study Yasuno, Fumihiko Kimura, Yasuyuki Ogata, Aya Ikenuma, Hiroshi Abe, Junichiro Minami, Hiroyuki Nihashi, Takashi Yokoi, Kastunori Hattori, Saori Shimoda, Nobuyoshi Watanabe, Atsushi Kasuga, Kensaku Ikeuchi, Takeshi Takeda, Akinori Sakurai, Takashi Ito, Kengo Kato, Takashi Psychogeriatrics Original Articles BACKGROUND: The evaluation of (11)C‐DPA‐713 binding using positron emission tomography for quantifying the translocator protein can be a sensitive approach in determining the level of glial activation induced by neuroinflammation. Herein, we aimed to investigate the relationship between regional (11)C‐DPA713‐binding potential (BP(ND)) and neuropsychiatric symptoms (NPS) in amyloid‐positive Alzheimer's disease (AD) patients. METHODS: Fifteen AD patients were enrolled in this study. Correlations were evaluated between the (11)C‐DPA713‐BP(ND) and Neuropsychiatric Inventory Questionnaire (NPI‐Q) scores, including scores in its four domains: agitation, psychosis, affective, and apathy. (11)C‐DPA713‐BP(ND) values were compared between groups with and without the neuropsychiatric symptoms for which a relationship was observed in the abovementioned correlation analysis. RESULTS: A positive correlation was found between the severity of agitation and (11)C‐DPA713‐BP(ND) in the Braak 1–3 area, including the amygdala, hippocampal and parahippocampal regions, and lingual and fusiform areas. An increase in the (11)C‐DPA713‐BP(ND) was observed in AD patients with agitation. We did not find any significant effects of possible confounding factors, such as age, duration of illness, education, gender, Mini‐Mental State Examination score, cerebrospinal fluid amyloid β 42/40 ratio, and apolipoprotein E4 positivity, on either the (11)C‐DPA713‐BP(ND) or agitation score. CONCLUSIONS: Neuroinflammation in the medial temporal region and its neighbouring area was shown to be associated with the development of agitation symptoms in AD patients. Our findings extend those of previous studies showing an association between some NPS and inflammation, suggesting that immunologically based interventions for agitation can serve as an alternative treatment for dementia. John Wiley & Sons Australia, Ltd 2022-11-20 2023-01 /pmc/articles/PMC10100091/ /pubmed/36403981 http://dx.doi.org/10.1111/psyg.12915 Text en © 2022 The Authors. Psychogeriatrics published by John Wiley & Sons Australia, Ltd on behalf of Japanese Psychogeriatric Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Yasuno, Fumihiko Kimura, Yasuyuki Ogata, Aya Ikenuma, Hiroshi Abe, Junichiro Minami, Hiroyuki Nihashi, Takashi Yokoi, Kastunori Hattori, Saori Shimoda, Nobuyoshi Watanabe, Atsushi Kasuga, Kensaku Ikeuchi, Takeshi Takeda, Akinori Sakurai, Takashi Ito, Kengo Kato, Takashi Involvement of inflammation in the medial temporal region in the development of agitation in Alzheimer's disease: an in vivo positron emission tomography study |
title | Involvement of inflammation in the medial temporal region in the development of agitation in Alzheimer's disease: an in vivo positron emission tomography study |
title_full | Involvement of inflammation in the medial temporal region in the development of agitation in Alzheimer's disease: an in vivo positron emission tomography study |
title_fullStr | Involvement of inflammation in the medial temporal region in the development of agitation in Alzheimer's disease: an in vivo positron emission tomography study |
title_full_unstemmed | Involvement of inflammation in the medial temporal region in the development of agitation in Alzheimer's disease: an in vivo positron emission tomography study |
title_short | Involvement of inflammation in the medial temporal region in the development of agitation in Alzheimer's disease: an in vivo positron emission tomography study |
title_sort | involvement of inflammation in the medial temporal region in the development of agitation in alzheimer's disease: an in vivo positron emission tomography study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10100091/ https://www.ncbi.nlm.nih.gov/pubmed/36403981 http://dx.doi.org/10.1111/psyg.12915 |
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