Medial temporal lobe atrophy is independently associated with behavioural and psychological symptoms in Alzheimer's disease
Aim Evidence describing the contribution of cerebral white matter disease and medial temporal atrophy (MTA) to behavioural and psychological symptoms of dementia (BPSD) has been conflicting. The aim of this study was to assess the relationship of white matter hyperintensities (WMH) and MTA observed...
Gespeichert in:
Veröffentlicht in: | Psychogeriatrics 2019-01, Vol.19 (1), p.46-54 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 54 |
---|---|
container_issue | 1 |
container_start_page | 46 |
container_title | Psychogeriatrics |
container_volume | 19 |
creator | García‐Alberca, José María Florido, Mercedes Cáceres, Marta Sánchez‐Toro, Alicia Lara, José Pablo García‐Casares, Natalia |
description | Aim
Evidence describing the contribution of cerebral white matter disease and medial temporal atrophy (MTA) to behavioural and psychological symptoms of dementia (BPSD) has been conflicting. The aim of this study was to assess the relationship of white matter hyperintensities (WMH) and MTA observed on magnetic resonance imaging with BPSD among patients with Alzheimer's disease.
Methods
In a cross‐sectional study of a prospective cohort of patients attending a memory clinic, 46 patients with probable Alzheimer's disease (mean age: 72.38 ± 7.05 years) were studied. Sociodemographic, cognitive, and BPSD data were collected. BPSD were assessed using the Neuropsychiatric Inventory. Magnetic resonance imaging, WMH, and MTA were rated using the Scheltens scales for the assessment of signal hyperintensities and atrophy of medial temporal lobes. For multivariate analysis, two binary logistic regression analyses were carried out, with presence or absence of each BPSD as the dependent variable and with WMH or MTA as the predictor variable. Results of the logistic regression were analyzed to see if the significance of the WMH or MTA score was maintained in a model that factored in other possible confounding variables identified in univariate analysis.
Results
The results of binary logistic regression analysis showed that in models that accounted for confounding variables, increased total MTA was significantly associated with apathy (odds ratio = 1.605, adjusted P = 0.042) and disinhibition (odds ratio = 0.607, adjusted P = 0.042). WMH measures did not significantly predict any BPSD item.
Conclusions
These findings indicate that MTA potentially contributes to the aetiology of BPSD, and they provide evidence to support the hypothesis that Alzheimer's disease pathology itself can contribute to BPSD. |
doi_str_mv | 10.1111/psyg.12363 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2084914262</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2084914262</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4173-91e6c335191085f2da86b0395626731e75bfb4fa40039e8d4a9e09fcb86a10a53</originalsourceid><addsrcrecordid>eNp9kUtLxDAUhYMoOo5u_AEScKEI1TzatF0Ogy9QFNSFq5C2tzZD2tSm41D982ac0YULs0guly-Hc-9B6ICSM-rPeeuG1zPKuOAbaETDOA0STuimr3koAh4RsoN2nZsRwsKI8220wwlJQhrHI_R5B4VWBvdQt7bzhbEZYNV3tq0GrB3WTQEt-KvpzYCVczbXqocCL3Rf4Qwq9a7tfPlTNQX2VvLKGvuqc99xQ932tl6K4In5qEDX0B07XGgHysEe2iqVcbC_fsfo-fLiaXod3N5f3Uwnt0HuPfIgpSByziOaUpJEJStUIjLC00gwEXMKcZSVWViqkPgmJEWoUiBpmWeJUJSoiI_RyUq37ezbHFwva-1yMEY1YOdOMr-MlIZMMI8e_UFnfrjGu5OMipQKznjsqdMVlXfWuQ5K2Xa6Vt0gKZHLSOQyEvkdiYcP15LzrIbiF_3JwAN0BSy0geEfKfnw-HK1Ev0CWVCX8g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2169163237</pqid></control><display><type>article</type><title>Medial temporal lobe atrophy is independently associated with behavioural and psychological symptoms in Alzheimer's disease</title><source>Wiley Online Library All Journals</source><creator>García‐Alberca, José María ; Florido, Mercedes ; Cáceres, Marta ; Sánchez‐Toro, Alicia ; Lara, José Pablo ; García‐Casares, Natalia</creator><creatorcontrib>García‐Alberca, José María ; Florido, Mercedes ; Cáceres, Marta ; Sánchez‐Toro, Alicia ; Lara, José Pablo ; García‐Casares, Natalia</creatorcontrib><description>Aim
Evidence describing the contribution of cerebral white matter disease and medial temporal atrophy (MTA) to behavioural and psychological symptoms of dementia (BPSD) has been conflicting. The aim of this study was to assess the relationship of white matter hyperintensities (WMH) and MTA observed on magnetic resonance imaging with BPSD among patients with Alzheimer's disease.
Methods
In a cross‐sectional study of a prospective cohort of patients attending a memory clinic, 46 patients with probable Alzheimer's disease (mean age: 72.38 ± 7.05 years) were studied. Sociodemographic, cognitive, and BPSD data were collected. BPSD were assessed using the Neuropsychiatric Inventory. Magnetic resonance imaging, WMH, and MTA were rated using the Scheltens scales for the assessment of signal hyperintensities and atrophy of medial temporal lobes. For multivariate analysis, two binary logistic regression analyses were carried out, with presence or absence of each BPSD as the dependent variable and with WMH or MTA as the predictor variable. Results of the logistic regression were analyzed to see if the significance of the WMH or MTA score was maintained in a model that factored in other possible confounding variables identified in univariate analysis.
Results
The results of binary logistic regression analysis showed that in models that accounted for confounding variables, increased total MTA was significantly associated with apathy (odds ratio = 1.605, adjusted P = 0.042) and disinhibition (odds ratio = 0.607, adjusted P = 0.042). WMH measures did not significantly predict any BPSD item.
Conclusions
These findings indicate that MTA potentially contributes to the aetiology of BPSD, and they provide evidence to support the hypothesis that Alzheimer's disease pathology itself can contribute to BPSD.</description><identifier>ISSN: 1346-3500</identifier><identifier>EISSN: 1479-8301</identifier><identifier>DOI: 10.1111/psyg.12363</identifier><identifier>PMID: 30084177</identifier><language>eng</language><publisher>Melbourne: John Wiley & Sons Australia, Ltd</publisher><subject>Alzheimer's disease ; Atrophy ; behavioural and psychological symptoms of dementia ; Cognitive ability ; Dementia disorders ; Emotional behavior ; Magnetic resonance imaging ; medial temporal lobe atrophy ; Memory ; Multivariate analysis ; Neurodegenerative diseases ; NMR ; Nuclear magnetic resonance ; Regression analysis ; Substantia alba ; Temporal lobe ; white matter hyperintensities</subject><ispartof>Psychogeriatrics, 2019-01, Vol.19 (1), p.46-54</ispartof><rights>2018 Japanese Psychogeriatric Society</rights><rights>2018 Japanese Psychogeriatric Society.</rights><rights>2019 Japanese Psychogeriatric Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4173-91e6c335191085f2da86b0395626731e75bfb4fa40039e8d4a9e09fcb86a10a53</citedby><cites>FETCH-LOGICAL-c4173-91e6c335191085f2da86b0395626731e75bfb4fa40039e8d4a9e09fcb86a10a53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fpsyg.12363$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fpsyg.12363$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30084177$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>García‐Alberca, José María</creatorcontrib><creatorcontrib>Florido, Mercedes</creatorcontrib><creatorcontrib>Cáceres, Marta</creatorcontrib><creatorcontrib>Sánchez‐Toro, Alicia</creatorcontrib><creatorcontrib>Lara, José Pablo</creatorcontrib><creatorcontrib>García‐Casares, Natalia</creatorcontrib><title>Medial temporal lobe atrophy is independently associated with behavioural and psychological symptoms in Alzheimer's disease</title><title>Psychogeriatrics</title><addtitle>Psychogeriatrics</addtitle><description>Aim
Evidence describing the contribution of cerebral white matter disease and medial temporal atrophy (MTA) to behavioural and psychological symptoms of dementia (BPSD) has been conflicting. The aim of this study was to assess the relationship of white matter hyperintensities (WMH) and MTA observed on magnetic resonance imaging with BPSD among patients with Alzheimer's disease.
Methods
In a cross‐sectional study of a prospective cohort of patients attending a memory clinic, 46 patients with probable Alzheimer's disease (mean age: 72.38 ± 7.05 years) were studied. Sociodemographic, cognitive, and BPSD data were collected. BPSD were assessed using the Neuropsychiatric Inventory. Magnetic resonance imaging, WMH, and MTA were rated using the Scheltens scales for the assessment of signal hyperintensities and atrophy of medial temporal lobes. For multivariate analysis, two binary logistic regression analyses were carried out, with presence or absence of each BPSD as the dependent variable and with WMH or MTA as the predictor variable. Results of the logistic regression were analyzed to see if the significance of the WMH or MTA score was maintained in a model that factored in other possible confounding variables identified in univariate analysis.
Results
The results of binary logistic regression analysis showed that in models that accounted for confounding variables, increased total MTA was significantly associated with apathy (odds ratio = 1.605, adjusted P = 0.042) and disinhibition (odds ratio = 0.607, adjusted P = 0.042). WMH measures did not significantly predict any BPSD item.
Conclusions
These findings indicate that MTA potentially contributes to the aetiology of BPSD, and they provide evidence to support the hypothesis that Alzheimer's disease pathology itself can contribute to BPSD.</description><subject>Alzheimer's disease</subject><subject>Atrophy</subject><subject>behavioural and psychological symptoms of dementia</subject><subject>Cognitive ability</subject><subject>Dementia disorders</subject><subject>Emotional behavior</subject><subject>Magnetic resonance imaging</subject><subject>medial temporal lobe atrophy</subject><subject>Memory</subject><subject>Multivariate analysis</subject><subject>Neurodegenerative diseases</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Regression analysis</subject><subject>Substantia alba</subject><subject>Temporal lobe</subject><subject>white matter hyperintensities</subject><issn>1346-3500</issn><issn>1479-8301</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kUtLxDAUhYMoOo5u_AEScKEI1TzatF0Ogy9QFNSFq5C2tzZD2tSm41D982ac0YULs0guly-Hc-9B6ICSM-rPeeuG1zPKuOAbaETDOA0STuimr3koAh4RsoN2nZsRwsKI8220wwlJQhrHI_R5B4VWBvdQt7bzhbEZYNV3tq0GrB3WTQEt-KvpzYCVczbXqocCL3Rf4Qwq9a7tfPlTNQX2VvLKGvuqc99xQ932tl6K4In5qEDX0B07XGgHysEe2iqVcbC_fsfo-fLiaXod3N5f3Uwnt0HuPfIgpSByziOaUpJEJStUIjLC00gwEXMKcZSVWViqkPgmJEWoUiBpmWeJUJSoiI_RyUq37ezbHFwva-1yMEY1YOdOMr-MlIZMMI8e_UFnfrjGu5OMipQKznjsqdMVlXfWuQ5K2Xa6Vt0gKZHLSOQyEvkdiYcP15LzrIbiF_3JwAN0BSy0geEfKfnw-HK1Ev0CWVCX8g</recordid><startdate>201901</startdate><enddate>201901</enddate><creator>García‐Alberca, José María</creator><creator>Florido, Mercedes</creator><creator>Cáceres, Marta</creator><creator>Sánchez‐Toro, Alicia</creator><creator>Lara, José Pablo</creator><creator>García‐Casares, Natalia</creator><general>John Wiley & Sons Australia, Ltd</general><general>Blackwell Publishing Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>201901</creationdate><title>Medial temporal lobe atrophy is independently associated with behavioural and psychological symptoms in Alzheimer's disease</title><author>García‐Alberca, José María ; Florido, Mercedes ; Cáceres, Marta ; Sánchez‐Toro, Alicia ; Lara, José Pablo ; García‐Casares, Natalia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4173-91e6c335191085f2da86b0395626731e75bfb4fa40039e8d4a9e09fcb86a10a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Alzheimer's disease</topic><topic>Atrophy</topic><topic>behavioural and psychological symptoms of dementia</topic><topic>Cognitive ability</topic><topic>Dementia disorders</topic><topic>Emotional behavior</topic><topic>Magnetic resonance imaging</topic><topic>medial temporal lobe atrophy</topic><topic>Memory</topic><topic>Multivariate analysis</topic><topic>Neurodegenerative diseases</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Regression analysis</topic><topic>Substantia alba</topic><topic>Temporal lobe</topic><topic>white matter hyperintensities</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>García‐Alberca, José María</creatorcontrib><creatorcontrib>Florido, Mercedes</creatorcontrib><creatorcontrib>Cáceres, Marta</creatorcontrib><creatorcontrib>Sánchez‐Toro, Alicia</creatorcontrib><creatorcontrib>Lara, José Pablo</creatorcontrib><creatorcontrib>García‐Casares, Natalia</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Psychogeriatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>García‐Alberca, José María</au><au>Florido, Mercedes</au><au>Cáceres, Marta</au><au>Sánchez‐Toro, Alicia</au><au>Lara, José Pablo</au><au>García‐Casares, Natalia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Medial temporal lobe atrophy is independently associated with behavioural and psychological symptoms in Alzheimer's disease</atitle><jtitle>Psychogeriatrics</jtitle><addtitle>Psychogeriatrics</addtitle><date>2019-01</date><risdate>2019</risdate><volume>19</volume><issue>1</issue><spage>46</spage><epage>54</epage><pages>46-54</pages><issn>1346-3500</issn><eissn>1479-8301</eissn><abstract>Aim
Evidence describing the contribution of cerebral white matter disease and medial temporal atrophy (MTA) to behavioural and psychological symptoms of dementia (BPSD) has been conflicting. The aim of this study was to assess the relationship of white matter hyperintensities (WMH) and MTA observed on magnetic resonance imaging with BPSD among patients with Alzheimer's disease.
Methods
In a cross‐sectional study of a prospective cohort of patients attending a memory clinic, 46 patients with probable Alzheimer's disease (mean age: 72.38 ± 7.05 years) were studied. Sociodemographic, cognitive, and BPSD data were collected. BPSD were assessed using the Neuropsychiatric Inventory. Magnetic resonance imaging, WMH, and MTA were rated using the Scheltens scales for the assessment of signal hyperintensities and atrophy of medial temporal lobes. For multivariate analysis, two binary logistic regression analyses were carried out, with presence or absence of each BPSD as the dependent variable and with WMH or MTA as the predictor variable. Results of the logistic regression were analyzed to see if the significance of the WMH or MTA score was maintained in a model that factored in other possible confounding variables identified in univariate analysis.
Results
The results of binary logistic regression analysis showed that in models that accounted for confounding variables, increased total MTA was significantly associated with apathy (odds ratio = 1.605, adjusted P = 0.042) and disinhibition (odds ratio = 0.607, adjusted P = 0.042). WMH measures did not significantly predict any BPSD item.
Conclusions
These findings indicate that MTA potentially contributes to the aetiology of BPSD, and they provide evidence to support the hypothesis that Alzheimer's disease pathology itself can contribute to BPSD.</abstract><cop>Melbourne</cop><pub>John Wiley & Sons Australia, Ltd</pub><pmid>30084177</pmid><doi>10.1111/psyg.12363</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1346-3500 |
ispartof | Psychogeriatrics, 2019-01, Vol.19 (1), p.46-54 |
issn | 1346-3500 1479-8301 |
language | eng |
recordid | cdi_proquest_miscellaneous_2084914262 |
source | Wiley Online Library All Journals |
subjects | Alzheimer's disease Atrophy behavioural and psychological symptoms of dementia Cognitive ability Dementia disorders Emotional behavior Magnetic resonance imaging medial temporal lobe atrophy Memory Multivariate analysis Neurodegenerative diseases NMR Nuclear magnetic resonance Regression analysis Substantia alba Temporal lobe white matter hyperintensities |
title | Medial temporal lobe atrophy is independently associated with behavioural and psychological symptoms in Alzheimer's disease |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T21%3A37%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Medial%20temporal%20lobe%20atrophy%20is%20independently%20associated%20with%20behavioural%20and%20psychological%20symptoms%20in%20Alzheimer's%20disease&rft.jtitle=Psychogeriatrics&rft.au=Garc%C3%ADa%E2%80%90Alberca,%20Jos%C3%A9%20Mar%C3%ADa&rft.date=2019-01&rft.volume=19&rft.issue=1&rft.spage=46&rft.epage=54&rft.pages=46-54&rft.issn=1346-3500&rft.eissn=1479-8301&rft_id=info:doi/10.1111/psyg.12363&rft_dat=%3Cproquest_cross%3E2084914262%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2169163237&rft_id=info:pmid/30084177&rfr_iscdi=true |