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...

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Veröffentlicht in:Psychogeriatrics 2019-01, Vol.19 (1), p.46-54
Hauptverfasser: García‐Alberca, José María, Florido, Mercedes, Cáceres, Marta, Sánchez‐Toro, Alicia, Lara, José Pablo, García‐Casares, Natalia
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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
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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 &amp; 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 &amp; 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 &amp; Sons Australia, Ltd</pub><pmid>30084177</pmid><doi>10.1111/psyg.12363</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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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
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