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Cognitive Change during the Life Course and Leukocyte Telomere Length in Late Middle-Aged Men
Cognitive skills are known to decline through the lifespan with large individual differences. The molecular mechanisms for this decline are incompletely understood. Although leukocyte telomere length provides an index of cellular age that predicts the incidence of age-related diseases, it is unclear...
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Published in: | Frontiers in aging neuroscience 2016-12, Vol.8, p.300-300 |
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description | Cognitive skills are known to decline through the lifespan with large individual differences. The molecular mechanisms for this decline are incompletely understood. Although leukocyte telomere length provides an index of cellular age that predicts the incidence of age-related diseases, it is unclear whether there is an association between cognitive decline and leukocyte telomere length.
To examine the association between changes in cognitive function during adult life and leukocyte telomere length after adjusting for confounding factors such as education, mental health and life style.
Two groups of men with negative (
= 97) and positive (
= 93) change in cognitive performance were selected from a birth cohort of 1985 Danish men born in 1953. Cognitive performance of each individual was assessed at age ~20 and 56 years. Leukocyte telomere length at age ~58 was measured using qPCR. Linear regression models were used to investigate the association between cognitive function and leukocyte telomere length.
Men with negative change in cognitive performance during adult life had significantly shorter mean leukocyte telomere length than men with positive change in cognitive performance (unadjusted difference β = -0.09, 95% CI -0.16 to -0.02,
= 0.02). This association remained significant after adjusting for smoking, alcohol consumption, leisure time activity, body mass index (BMI) and cholesterol (adjusted difference β = -0.09, 95% CI -0.17 to -0.01,
= 0.02) but was non-significant after adjusting for smoking, alcohol consumption, leisure time activity, BMI, cholesterol, current cognitive function, depression and education (adjusted difference β = -0.07, 95% CI -0.16 to -0.01,
= 0.08).
Preclinical cognitive changes may be associated with leukocyte telomere length. |
doi_str_mv | 10.3389/fnagi.2016.00300 |
format | article |
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To examine the association between changes in cognitive function during adult life and leukocyte telomere length after adjusting for confounding factors such as education, mental health and life style.
Two groups of men with negative (
= 97) and positive (
= 93) change in cognitive performance were selected from a birth cohort of 1985 Danish men born in 1953. Cognitive performance of each individual was assessed at age ~20 and 56 years. Leukocyte telomere length at age ~58 was measured using qPCR. Linear regression models were used to investigate the association between cognitive function and leukocyte telomere length.
Men with negative change in cognitive performance during adult life had significantly shorter mean leukocyte telomere length than men with positive change in cognitive performance (unadjusted difference β = -0.09, 95% CI -0.16 to -0.02,
= 0.02). This association remained significant after adjusting for smoking, alcohol consumption, leisure time activity, body mass index (BMI) and cholesterol (adjusted difference β = -0.09, 95% CI -0.17 to -0.01,
= 0.02) but was non-significant after adjusting for smoking, alcohol consumption, leisure time activity, BMI, cholesterol, current cognitive function, depression and education (adjusted difference β = -0.07, 95% CI -0.16 to -0.01,
= 0.08).
Preclinical cognitive changes may be associated with leukocyte telomere length.</description><identifier>ISSN: 1663-4365</identifier><identifier>EISSN: 1663-4365</identifier><identifier>DOI: 10.3389/fnagi.2016.00300</identifier><identifier>PMID: 28018213</identifier><language>eng</language><publisher>Switzerland: Frontiers Research Foundation</publisher><subject>Adults ; Age ; Aging ; Alcohol ; Alzheimer's disease ; Birth cohort study ; Body mass index ; Cholesterol ; Cognitive ability ; Cognitive Function ; Cohort analysis ; Dementia ; Health care ; Inflammation ; Life span ; Mental disorders ; Mental Health ; Molecular modelling ; Neuroscience ; Oxidative stress ; Public health ; Regression analysis ; Schizophrenia ; Smoking ; telomere length</subject><ispartof>Frontiers in aging neuroscience, 2016-12, Vol.8, p.300-300</ispartof><rights>2016. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2016 Rask, Bendix, Harbo, Fagerlund, Mortensen, Lauritzen and Osler. 2016 Rask, Bendix, Harbo, Fagerlund, Mortensen, Lauritzen and Osler</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-a409da5a6c51e5f7f7f8ea6f33cbfcdfe50d4ac76ac1b31c226057d8f30068123</citedby><cites>FETCH-LOGICAL-c490t-a409da5a6c51e5f7f7f8ea6f33cbfcdfe50d4ac76ac1b31c226057d8f30068123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2301486325/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2301486325?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28018213$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rask, Lene</creatorcontrib><creatorcontrib>Bendix, Laila</creatorcontrib><creatorcontrib>Harbo, Maria</creatorcontrib><creatorcontrib>Fagerlund, Birgitte</creatorcontrib><creatorcontrib>Mortensen, Erik L</creatorcontrib><creatorcontrib>Lauritzen, Martin J</creatorcontrib><creatorcontrib>Osler, Merete</creatorcontrib><title>Cognitive Change during the Life Course and Leukocyte Telomere Length in Late Middle-Aged Men</title><title>Frontiers in aging neuroscience</title><addtitle>Front Aging Neurosci</addtitle><description>Cognitive skills are known to decline through the lifespan with large individual differences. The molecular mechanisms for this decline are incompletely understood. Although leukocyte telomere length provides an index of cellular age that predicts the incidence of age-related diseases, it is unclear whether there is an association between cognitive decline and leukocyte telomere length.
To examine the association between changes in cognitive function during adult life and leukocyte telomere length after adjusting for confounding factors such as education, mental health and life style.
Two groups of men with negative (
= 97) and positive (
= 93) change in cognitive performance were selected from a birth cohort of 1985 Danish men born in 1953. Cognitive performance of each individual was assessed at age ~20 and 56 years. Leukocyte telomere length at age ~58 was measured using qPCR. Linear regression models were used to investigate the association between cognitive function and leukocyte telomere length.
Men with negative change in cognitive performance during adult life had significantly shorter mean leukocyte telomere length than men with positive change in cognitive performance (unadjusted difference β = -0.09, 95% CI -0.16 to -0.02,
= 0.02). This association remained significant after adjusting for smoking, alcohol consumption, leisure time activity, body mass index (BMI) and cholesterol (adjusted difference β = -0.09, 95% CI -0.17 to -0.01,
= 0.02) but was non-significant after adjusting for smoking, alcohol consumption, leisure time activity, BMI, cholesterol, current cognitive function, depression and education (adjusted difference β = -0.07, 95% CI -0.16 to -0.01,
= 0.08).
Preclinical cognitive changes may be associated with leukocyte telomere length.</description><subject>Adults</subject><subject>Age</subject><subject>Aging</subject><subject>Alcohol</subject><subject>Alzheimer's disease</subject><subject>Birth cohort study</subject><subject>Body mass index</subject><subject>Cholesterol</subject><subject>Cognitive ability</subject><subject>Cognitive Function</subject><subject>Cohort analysis</subject><subject>Dementia</subject><subject>Health care</subject><subject>Inflammation</subject><subject>Life span</subject><subject>Mental disorders</subject><subject>Mental Health</subject><subject>Molecular modelling</subject><subject>Neuroscience</subject><subject>Oxidative stress</subject><subject>Public health</subject><subject>Regression analysis</subject><subject>Schizophrenia</subject><subject>Smoking</subject><subject>telomere length</subject><issn>1663-4365</issn><issn>1663-4365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk1r3DAQhk1paUKae0_F0Esv3krWh-VLISxpG3DIJT0WMZZGXm29Uirbgfz7anfTkEQ6SIyeeZkZvUXxkZIVY6r96gIMflUTKleEMELeFKdUSlZxJsXbZ_eT4nyatiQvlimh3hcntSJU1ZSdFr_XcQh-9vdYrjcQBiztknwYynmDZeddDsclTVhCsGWHy59oHmYsb3GMO0wZwTDMm9KHsoMcv_bWjlhdDGjLawwfincOxgnPH8-z4tf3y9v1z6q7-XG1vugqw1syV8BJa0GANIKicE3eCkE6xkzvjHUoiOVgGgmG9oyaupZENFa53I9UtGZnxdVR10bY6rvkd5AedASvD4GYBg1p9mZEzdFITlsnOKG8B6tU65hh0EDTN87wrPXtqHW39Du0BsOcYHwh-vIl-I0e4r0WlAslaBb48iiQ4t8Fp1nv_GRwHCFgXCZNlWCMty3fo59fods87ZBHpWuW61OS1SJT5EiZFKcpoXsqhhK9t4I-WEHvraAPVsgpn5438ZTw_-PZP_akr6A</recordid><startdate>20161209</startdate><enddate>20161209</enddate><creator>Rask, Lene</creator><creator>Bendix, Laila</creator><creator>Harbo, Maria</creator><creator>Fagerlund, Birgitte</creator><creator>Mortensen, Erik L</creator><creator>Lauritzen, Martin J</creator><creator>Osler, Merete</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>20161209</creationdate><title>Cognitive Change during the Life Course and Leukocyte Telomere Length in Late Middle-Aged Men</title><author>Rask, Lene ; Bendix, Laila ; Harbo, Maria ; Fagerlund, Birgitte ; Mortensen, Erik L ; Lauritzen, Martin J ; Osler, Merete</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-a409da5a6c51e5f7f7f8ea6f33cbfcdfe50d4ac76ac1b31c226057d8f30068123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adults</topic><topic>Age</topic><topic>Aging</topic><topic>Alcohol</topic><topic>Alzheimer's disease</topic><topic>Birth cohort study</topic><topic>Body mass index</topic><topic>Cholesterol</topic><topic>Cognitive ability</topic><topic>Cognitive Function</topic><topic>Cohort analysis</topic><topic>Dementia</topic><topic>Health care</topic><topic>Inflammation</topic><topic>Life span</topic><topic>Mental disorders</topic><topic>Mental Health</topic><topic>Molecular modelling</topic><topic>Neuroscience</topic><topic>Oxidative stress</topic><topic>Public health</topic><topic>Regression analysis</topic><topic>Schizophrenia</topic><topic>Smoking</topic><topic>telomere length</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rask, Lene</creatorcontrib><creatorcontrib>Bendix, Laila</creatorcontrib><creatorcontrib>Harbo, Maria</creatorcontrib><creatorcontrib>Fagerlund, Birgitte</creatorcontrib><creatorcontrib>Mortensen, Erik L</creatorcontrib><creatorcontrib>Lauritzen, Martin J</creatorcontrib><creatorcontrib>Osler, Merete</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest 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 UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: 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>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>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>Open Access: 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>Rask, Lene</au><au>Bendix, Laila</au><au>Harbo, Maria</au><au>Fagerlund, Birgitte</au><au>Mortensen, Erik L</au><au>Lauritzen, Martin J</au><au>Osler, Merete</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cognitive Change during the Life Course and Leukocyte Telomere Length in Late Middle-Aged Men</atitle><jtitle>Frontiers in aging neuroscience</jtitle><addtitle>Front Aging Neurosci</addtitle><date>2016-12-09</date><risdate>2016</risdate><volume>8</volume><spage>300</spage><epage>300</epage><pages>300-300</pages><issn>1663-4365</issn><eissn>1663-4365</eissn><abstract>Cognitive skills are known to decline through the lifespan with large individual differences. The molecular mechanisms for this decline are incompletely understood. Although leukocyte telomere length provides an index of cellular age that predicts the incidence of age-related diseases, it is unclear whether there is an association between cognitive decline and leukocyte telomere length.
To examine the association between changes in cognitive function during adult life and leukocyte telomere length after adjusting for confounding factors such as education, mental health and life style.
Two groups of men with negative (
= 97) and positive (
= 93) change in cognitive performance were selected from a birth cohort of 1985 Danish men born in 1953. Cognitive performance of each individual was assessed at age ~20 and 56 years. Leukocyte telomere length at age ~58 was measured using qPCR. Linear regression models were used to investigate the association between cognitive function and leukocyte telomere length.
Men with negative change in cognitive performance during adult life had significantly shorter mean leukocyte telomere length than men with positive change in cognitive performance (unadjusted difference β = -0.09, 95% CI -0.16 to -0.02,
= 0.02). This association remained significant after adjusting for smoking, alcohol consumption, leisure time activity, body mass index (BMI) and cholesterol (adjusted difference β = -0.09, 95% CI -0.17 to -0.01,
= 0.02) but was non-significant after adjusting for smoking, alcohol consumption, leisure time activity, BMI, cholesterol, current cognitive function, depression and education (adjusted difference β = -0.07, 95% CI -0.16 to -0.01,
= 0.08).
Preclinical cognitive changes may be associated with leukocyte telomere length.</abstract><cop>Switzerland</cop><pub>Frontiers Research Foundation</pub><pmid>28018213</pmid><doi>10.3389/fnagi.2016.00300</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adults Age Aging Alcohol Alzheimer's disease Birth cohort study Body mass index Cholesterol Cognitive ability Cognitive Function Cohort analysis Dementia Health care Inflammation Life span Mental disorders Mental Health Molecular modelling Neuroscience Oxidative stress Public health Regression analysis Schizophrenia Smoking telomere length |
title | Cognitive Change during the Life Course and Leukocyte Telomere Length in Late Middle-Aged Men |
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