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Plasma omega-3 PUFA and white matter mediated executive decline in older adults
Cross-sectional studies have identified long chain omega-3 polyunsaturated fatty acids (eicosapentaenoic acid 20:5n-3 and docosahexaenoic acid 22:6n-3 (O3PUFA) in association with fewer white matter lesions and better executive function in older adults. We hypothesized that O3PUFA are associated wit...
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Published in: | Frontiers in aging neuroscience 2013, Vol.5, p.92-92 |
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creator | Bowman, Gene L Dodge, Hiroko H Mattek, Nora Barbey, Aron K Silbert, Lisa C Shinto, Lynne Howieson, Diane B Kaye, Jeffrey A Quinn, Joseph F |
description | Cross-sectional studies have identified long chain omega-3 polyunsaturated fatty acids (eicosapentaenoic acid 20:5n-3 and docosahexaenoic acid 22:6n-3 (O3PUFA) in association with fewer white matter lesions and better executive function in older adults. We hypothesized that O3PUFA are associated with less executive decline over time and that total white matter hyperintensity volume (WMH) mediates this association.
Eighty-six non-demented older adults were followed over 4 years after measurement of plasma O3PUFA with annual evaluations of cognitive function. A subset of these participants also had brain MRI of total WMH available to conduct a formal mediation analysis of a putative relationship between O3PUFA and cognitive function.
Mean age at baseline was 86, 62% were female and 11% carried the APOE4 allele. Each 100 μg/ml increase in plasma O3PUFA associated with 4 s less change in executive decline per year of aging (p = 0.02, fully adjusted model). O3PUFA was not associated with verbal memory or global cognitive changes. The significance of the association between O3PUFA and better executive function was lost once WMH was added to the regression model.
Executive decline with age appears to be a cognitive domain particularly sensitive to plasma O3PUFA in longitudinal examination. O3PUFA may modulate executive functioning by mechanisms underlying the development of WMH, a biologically plausible hypothesis that warrants further investigation. |
doi_str_mv | 10.3389/fnagi.2013.00092 |
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Eighty-six non-demented older adults were followed over 4 years after measurement of plasma O3PUFA with annual evaluations of cognitive function. A subset of these participants also had brain MRI of total WMH available to conduct a formal mediation analysis of a putative relationship between O3PUFA and cognitive function.
Mean age at baseline was 86, 62% were female and 11% carried the APOE4 allele. Each 100 μg/ml increase in plasma O3PUFA associated with 4 s less change in executive decline per year of aging (p = 0.02, fully adjusted model). O3PUFA was not associated with verbal memory or global cognitive changes. The significance of the association between O3PUFA and better executive function was lost once WMH was added to the regression model.
Executive decline with age appears to be a cognitive domain particularly sensitive to plasma O3PUFA in longitudinal examination. O3PUFA may modulate executive functioning by mechanisms underlying the development of WMH, a biologically plausible hypothesis that warrants further investigation.</description><identifier>ISSN: 1663-4365</identifier><identifier>EISSN: 1663-4365</identifier><identifier>DOI: 10.3389/fnagi.2013.00092</identifier><identifier>PMID: 24379780</identifier><language>eng</language><publisher>Switzerland: Frontiers Research Foundation</publisher><subject>Age ; Aging ; Alzheimer's disease ; Apolipoprotein E4 ; Biomarkers ; Blood ; Cognition & reasoning ; Cognitive ability ; cognitive decline ; Dementia ; Diabetes ; Docosahexaenoic acid ; Eicosapentaenoic acid ; Elderly ; Executive Function ; Fatty acids ; Hypertension ; Lipid Metabolism ; longitudinal data analysis ; Magnetic resonance imaging ; MRI ; Neurology ; Neuroscience ; Older people ; Plasma ; Polyunsaturated fatty acids ; Substantia alba</subject><ispartof>Frontiers in aging neuroscience, 2013, Vol.5, p.92-92</ispartof><rights>2013. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2013 Bowman, Dodge, Mattek, Barbey, Silbert, Shinto, Howieson, Kaye and Quinn. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c556t-b7f5ce425568e80b7b3d7d45d1f8b0dd5e69be78c6d9c0f0737da2c248c98dfe3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2301955451/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2301955451?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,25753,27923,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24379780$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bowman, Gene L</creatorcontrib><creatorcontrib>Dodge, Hiroko H</creatorcontrib><creatorcontrib>Mattek, Nora</creatorcontrib><creatorcontrib>Barbey, Aron K</creatorcontrib><creatorcontrib>Silbert, Lisa C</creatorcontrib><creatorcontrib>Shinto, Lynne</creatorcontrib><creatorcontrib>Howieson, Diane B</creatorcontrib><creatorcontrib>Kaye, Jeffrey A</creatorcontrib><creatorcontrib>Quinn, Joseph F</creatorcontrib><title>Plasma omega-3 PUFA and white matter mediated executive decline in older adults</title><title>Frontiers in aging neuroscience</title><addtitle>Front Aging Neurosci</addtitle><description>Cross-sectional studies have identified long chain omega-3 polyunsaturated fatty acids (eicosapentaenoic acid 20:5n-3 and docosahexaenoic acid 22:6n-3 (O3PUFA) in association with fewer white matter lesions and better executive function in older adults. We hypothesized that O3PUFA are associated with less executive decline over time and that total white matter hyperintensity volume (WMH) mediates this association.
Eighty-six non-demented older adults were followed over 4 years after measurement of plasma O3PUFA with annual evaluations of cognitive function. A subset of these participants also had brain MRI of total WMH available to conduct a formal mediation analysis of a putative relationship between O3PUFA and cognitive function.
Mean age at baseline was 86, 62% were female and 11% carried the APOE4 allele. Each 100 μg/ml increase in plasma O3PUFA associated with 4 s less change in executive decline per year of aging (p = 0.02, fully adjusted model). O3PUFA was not associated with verbal memory or global cognitive changes. The significance of the association between O3PUFA and better executive function was lost once WMH was added to the regression model.
Executive decline with age appears to be a cognitive domain particularly sensitive to plasma O3PUFA in longitudinal examination. O3PUFA may modulate executive functioning by mechanisms underlying the development of WMH, a biologically plausible hypothesis that warrants further investigation.</description><subject>Age</subject><subject>Aging</subject><subject>Alzheimer's disease</subject><subject>Apolipoprotein E4</subject><subject>Biomarkers</subject><subject>Blood</subject><subject>Cognition & reasoning</subject><subject>Cognitive ability</subject><subject>cognitive decline</subject><subject>Dementia</subject><subject>Diabetes</subject><subject>Docosahexaenoic acid</subject><subject>Eicosapentaenoic acid</subject><subject>Elderly</subject><subject>Executive Function</subject><subject>Fatty acids</subject><subject>Hypertension</subject><subject>Lipid Metabolism</subject><subject>longitudinal data analysis</subject><subject>Magnetic resonance imaging</subject><subject>MRI</subject><subject>Neurology</subject><subject>Neuroscience</subject><subject>Older people</subject><subject>Plasma</subject><subject>Polyunsaturated fatty acids</subject><subject>Substantia alba</subject><issn>1663-4365</issn><issn>1663-4365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkc1PFDEYhxujEbJy92SaePEyazv9nIsJISIkJHCQc9Np3y7dzEyx7aD-987uAgEPTb-e90nf_hD6SMmaMd19DZPdxHVLKFsTQrr2DTqmUrKGMynevlgfoZNStgtCGCNE6PfoqOVMdUqTY3R9M9gyWpxG2NiG4Zvb81NsJ49_38UKeLS1QsYj-GgreAx_wM01PgD24IY4AY4TToNfGOvnoZYP6F2wQ4GTx3mFbs-__zy7aK6uf1yenV41TghZm14F4YC3y0aDJr3qmVeeC0-D7on3AmTXg9JO-s6RQBRT3rau5dp12gdgK3R58Ppkt-Y-x9HmvybZaPYHKW-MzTW6AQyIAFqBszr0vFNcB9p6R52UDkQvd65vB9f93C-dOphqtsMr6eubKd6ZTXowTEumlrFCXx4FOf2aoVQzxuJgGOwEaS6G8o4o2UrNF_Tzf-g2zXlavsq0jNBOCC7oQpED5XIqJUN4fgwlZhe-2YdvduGbffhLyaeXTTwXPEXN_gGo3avs</recordid><startdate>2013</startdate><enddate>2013</enddate><creator>Bowman, Gene L</creator><creator>Dodge, Hiroko H</creator><creator>Mattek, Nora</creator><creator>Barbey, Aron K</creator><creator>Silbert, Lisa C</creator><creator>Shinto, Lynne</creator><creator>Howieson, Diane B</creator><creator>Kaye, Jeffrey A</creator><creator>Quinn, Joseph F</creator><general>Frontiers Research Foundation</general><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>2013</creationdate><title>Plasma omega-3 PUFA and white matter mediated executive decline in older adults</title><author>Bowman, Gene L ; Dodge, Hiroko H ; Mattek, Nora ; Barbey, Aron K ; Silbert, Lisa C ; Shinto, Lynne ; Howieson, Diane B ; Kaye, Jeffrey A ; Quinn, Joseph F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c556t-b7f5ce425568e80b7b3d7d45d1f8b0dd5e69be78c6d9c0f0737da2c248c98dfe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Age</topic><topic>Aging</topic><topic>Alzheimer's disease</topic><topic>Apolipoprotein E4</topic><topic>Biomarkers</topic><topic>Blood</topic><topic>Cognition & reasoning</topic><topic>Cognitive ability</topic><topic>cognitive decline</topic><topic>Dementia</topic><topic>Diabetes</topic><topic>Docosahexaenoic acid</topic><topic>Eicosapentaenoic acid</topic><topic>Elderly</topic><topic>Executive Function</topic><topic>Fatty acids</topic><topic>Hypertension</topic><topic>Lipid Metabolism</topic><topic>longitudinal data analysis</topic><topic>Magnetic resonance imaging</topic><topic>MRI</topic><topic>Neurology</topic><topic>Neuroscience</topic><topic>Older people</topic><topic>Plasma</topic><topic>Polyunsaturated fatty acids</topic><topic>Substantia alba</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bowman, Gene L</creatorcontrib><creatorcontrib>Dodge, Hiroko H</creatorcontrib><creatorcontrib>Mattek, Nora</creatorcontrib><creatorcontrib>Barbey, Aron K</creatorcontrib><creatorcontrib>Silbert, Lisa C</creatorcontrib><creatorcontrib>Shinto, Lynne</creatorcontrib><creatorcontrib>Howieson, Diane B</creatorcontrib><creatorcontrib>Kaye, Jeffrey A</creatorcontrib><creatorcontrib>Quinn, Joseph F</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in aging neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bowman, Gene L</au><au>Dodge, Hiroko H</au><au>Mattek, Nora</au><au>Barbey, Aron K</au><au>Silbert, Lisa C</au><au>Shinto, Lynne</au><au>Howieson, Diane B</au><au>Kaye, Jeffrey A</au><au>Quinn, Joseph F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma omega-3 PUFA and white matter mediated executive decline in older adults</atitle><jtitle>Frontiers in aging neuroscience</jtitle><addtitle>Front Aging Neurosci</addtitle><date>2013</date><risdate>2013</risdate><volume>5</volume><spage>92</spage><epage>92</epage><pages>92-92</pages><issn>1663-4365</issn><eissn>1663-4365</eissn><abstract>Cross-sectional studies have identified long chain omega-3 polyunsaturated fatty acids (eicosapentaenoic acid 20:5n-3 and docosahexaenoic acid 22:6n-3 (O3PUFA) in association with fewer white matter lesions and better executive function in older adults. We hypothesized that O3PUFA are associated with less executive decline over time and that total white matter hyperintensity volume (WMH) mediates this association.
Eighty-six non-demented older adults were followed over 4 years after measurement of plasma O3PUFA with annual evaluations of cognitive function. A subset of these participants also had brain MRI of total WMH available to conduct a formal mediation analysis of a putative relationship between O3PUFA and cognitive function.
Mean age at baseline was 86, 62% were female and 11% carried the APOE4 allele. Each 100 μg/ml increase in plasma O3PUFA associated with 4 s less change in executive decline per year of aging (p = 0.02, fully adjusted model). O3PUFA was not associated with verbal memory or global cognitive changes. The significance of the association between O3PUFA and better executive function was lost once WMH was added to the regression model.
Executive decline with age appears to be a cognitive domain particularly sensitive to plasma O3PUFA in longitudinal examination. O3PUFA may modulate executive functioning by mechanisms underlying the development of WMH, a biologically plausible hypothesis that warrants further investigation.</abstract><cop>Switzerland</cop><pub>Frontiers Research Foundation</pub><pmid>24379780</pmid><doi>10.3389/fnagi.2013.00092</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Age Aging Alzheimer's disease Apolipoprotein E4 Biomarkers Blood Cognition & reasoning Cognitive ability cognitive decline Dementia Diabetes Docosahexaenoic acid Eicosapentaenoic acid Elderly Executive Function Fatty acids Hypertension Lipid Metabolism longitudinal data analysis Magnetic resonance imaging MRI Neurology Neuroscience Older people Plasma Polyunsaturated fatty acids Substantia alba |
title | Plasma omega-3 PUFA and white matter mediated executive decline in older adults |
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