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Current versus lifetime depression, APOE variation, and their interaction on cognitive performance in younger and older adults
An interaction effect of depressive symptoms and APOE e4 allele status on cognitive decline has been shown in old age: e4 allele carriers with more depressive symptoms have faster cognitive decline than those with either depression or the e4 allele. We test this interaction effect on four cognitive...
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Published in: | Psychosomatic medicine 2015-06, Vol.77 (5), p.480-492 |
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container_title | Psychosomatic medicine |
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creator | Luciano, Michelle Pujals, Ana Maria Fernández Marioni, Riccardo E Campbell, Archie Hayward, Caroline MacIntyre, Donald J Porteous, David J McIntosh, Andrew M Deary, Ian J |
description | An interaction effect of depressive symptoms and APOE e4 allele status on cognitive decline has been shown in old age: e4 allele carriers with more depressive symptoms have faster cognitive decline than those with either depression or the e4 allele. We test this interaction effect on four cognitive domains, using a clinical depression measure comparing current versus lifetime depression.
14,379 individuals aged 18 to 59 years, and 3944 individuals aged 60 to 94 years from the Generation Scotland: Scottish Family Health Study participated. Linear-mixed models-accounting for participant relatedness and demographic and health indices-tested for effects of depression and APOE on cognitive abilities.
There was no interaction between depression and APOE on cognition (p > .05). Current depression was associated with poorer speed (in both groups) and memory (18- to 59-year-olds); differences ranged from 0.01 to 0.03 standard deviation [SD]. For lifetime depression, cognitive performance was lower for digit symbol in younger adults, but higher for vocabulary in both younger (0.03 SD) and older (0.05 SD) adults. A negative effect of the APOE e4 allele on speed and memory was found in the group 60 years and older (effect sizes of 0.04 SD).
The absence of a depression by APOE interaction on cognitive abilities suggests that these synergistic effects only operate at the level of cognitive decline. This implies that it is those biological pathways especially affected by aging that become compromised further by the combined presence of depression and APOE e4 in an individual. |
doi_str_mv | 10.1097/PSY.0000000000000190 |
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14,379 individuals aged 18 to 59 years, and 3944 individuals aged 60 to 94 years from the Generation Scotland: Scottish Family Health Study participated. Linear-mixed models-accounting for participant relatedness and demographic and health indices-tested for effects of depression and APOE on cognitive abilities.
There was no interaction between depression and APOE on cognition (p > .05). Current depression was associated with poorer speed (in both groups) and memory (18- to 59-year-olds); differences ranged from 0.01 to 0.03 standard deviation [SD]. For lifetime depression, cognitive performance was lower for digit symbol in younger adults, but higher for vocabulary in both younger (0.03 SD) and older (0.05 SD) adults. A negative effect of the APOE e4 allele on speed and memory was found in the group 60 years and older (effect sizes of 0.04 SD).
The absence of a depression by APOE interaction on cognitive abilities suggests that these synergistic effects only operate at the level of cognitive decline. This implies that it is those biological pathways especially affected by aging that become compromised further by the combined presence of depression and APOE e4 in an individual.</description><identifier>ISSN: 0033-3174</identifier><identifier>EISSN: 1534-7796</identifier><identifier>DOI: 10.1097/PSY.0000000000000190</identifier><identifier>PMID: 26035038</identifier><identifier>CODEN: PSMEAP</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins Ovid Technologies</publisher><subject>Adolescent ; Adult ; Age differences ; Aged ; Aged, 80 and over ; Aging - physiology ; Apolipoprotein E4 - genetics ; Cognition - physiology ; Cognition Disorders - genetics ; Cognition Disorders - physiopathology ; Cognitive ability ; Depressive Disorder - genetics ; Depressive Disorder - physiopathology ; Female ; Gene loci ; Humans ; Male ; Memory ; Mental depression ; Middle Aged ; Psychosomatic medicine ; Scotland ; Time Factors ; Young Adult</subject><ispartof>Psychosomatic medicine, 2015-06, Vol.77 (5), p.480-492</ispartof><rights>Copyright Lippincott Williams & Wilkins Jun 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-f0978279c272c366490754f7627de701d1052edc0f481c08f9e82d601e460f53</citedby><cites>FETCH-LOGICAL-c414t-f0978279c272c366490754f7627de701d1052edc0f481c08f9e82d601e460f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27898,27899,30973</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26035038$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luciano, Michelle</creatorcontrib><creatorcontrib>Pujals, Ana Maria Fernández</creatorcontrib><creatorcontrib>Marioni, Riccardo E</creatorcontrib><creatorcontrib>Campbell, Archie</creatorcontrib><creatorcontrib>Hayward, Caroline</creatorcontrib><creatorcontrib>MacIntyre, Donald J</creatorcontrib><creatorcontrib>Porteous, David J</creatorcontrib><creatorcontrib>McIntosh, Andrew M</creatorcontrib><creatorcontrib>Deary, Ian J</creatorcontrib><creatorcontrib>Generation Scotland Investigators</creatorcontrib><title>Current versus lifetime depression, APOE variation, and their interaction on cognitive performance in younger and older adults</title><title>Psychosomatic medicine</title><addtitle>Psychosom Med</addtitle><description>An interaction effect of depressive symptoms and APOE e4 allele status on cognitive decline has been shown in old age: e4 allele carriers with more depressive symptoms have faster cognitive decline than those with either depression or the e4 allele. We test this interaction effect on four cognitive domains, using a clinical depression measure comparing current versus lifetime depression.
14,379 individuals aged 18 to 59 years, and 3944 individuals aged 60 to 94 years from the Generation Scotland: Scottish Family Health Study participated. Linear-mixed models-accounting for participant relatedness and demographic and health indices-tested for effects of depression and APOE on cognitive abilities.
There was no interaction between depression and APOE on cognition (p > .05). Current depression was associated with poorer speed (in both groups) and memory (18- to 59-year-olds); differences ranged from 0.01 to 0.03 standard deviation [SD]. For lifetime depression, cognitive performance was lower for digit symbol in younger adults, but higher for vocabulary in both younger (0.03 SD) and older (0.05 SD) adults. A negative effect of the APOE e4 allele on speed and memory was found in the group 60 years and older (effect sizes of 0.04 SD).
The absence of a depression by APOE interaction on cognitive abilities suggests that these synergistic effects only operate at the level of cognitive decline. This implies that it is those biological pathways especially affected by aging that become compromised further by the combined presence of depression and APOE e4 in an individual.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age differences</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging - physiology</subject><subject>Apolipoprotein E4 - genetics</subject><subject>Cognition - physiology</subject><subject>Cognition Disorders - genetics</subject><subject>Cognition Disorders - physiopathology</subject><subject>Cognitive ability</subject><subject>Depressive Disorder - genetics</subject><subject>Depressive Disorder - physiopathology</subject><subject>Female</subject><subject>Gene loci</subject><subject>Humans</subject><subject>Male</subject><subject>Memory</subject><subject>Mental depression</subject><subject>Middle Aged</subject><subject>Psychosomatic medicine</subject><subject>Scotland</subject><subject>Time Factors</subject><subject>Young Adult</subject><issn>0033-3174</issn><issn>1534-7796</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>7QJ</sourceid><recordid>eNqFkU1rFTEUhoNY7PXqPxAJuHHRqSeTTDJZlkutQqGFduNqGJOTmjKTXJPMhW787ea2VUo3DYF88LwvHB5CPjA4ZqDVl8urH8fwdDENr8iKdVw0Smn5mqwAOG84U-KQvM35tjJC8_YNOWwl8A54vyJ_NktKGArdYcpLppN3WPyM1OI2Yc4-hiN6cnlxSndj8mO5f4_B0vILfaI-FEyj2X_Tuk28Cb74HdItJhfTPAaDFaJ3cQk3mO6TcbL7m12mkt-RAzdOGd8_nmty_fX0evOtOb84-745OW-MYKI0rg7ct0qbVrWGSyk0qE44JVtlUQGzDLoWrQEnemagdxr71kpgKCS4jq_J54fabYq_F8xlmH02OE1jwLjkgdUOoaQS7GVU9lLrTktZ0U_P0Nu4pFDnqJRmoDivAtZEPFAmxZwTumGb_Dymu4HBsDc5VJPDc5M19vGxfPk5o_0f-qeO_wXUqJiD</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Luciano, Michelle</creator><creator>Pujals, Ana Maria Fernández</creator><creator>Marioni, Riccardo E</creator><creator>Campbell, Archie</creator><creator>Hayward, Caroline</creator><creator>MacIntyre, Donald J</creator><creator>Porteous, David J</creator><creator>McIntosh, Andrew M</creator><creator>Deary, Ian J</creator><general>Lippincott Williams & Wilkins Ovid Technologies</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20150601</creationdate><title>Current versus lifetime depression, APOE variation, and their interaction on cognitive performance in younger and older adults</title><author>Luciano, Michelle ; Pujals, Ana Maria Fernández ; Marioni, Riccardo E ; Campbell, Archie ; Hayward, Caroline ; MacIntyre, Donald J ; Porteous, David J ; McIntosh, Andrew M ; Deary, Ian J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-f0978279c272c366490754f7627de701d1052edc0f481c08f9e82d601e460f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age differences</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aging - physiology</topic><topic>Apolipoprotein E4 - genetics</topic><topic>Cognition - physiology</topic><topic>Cognition Disorders - genetics</topic><topic>Cognition Disorders - physiopathology</topic><topic>Cognitive ability</topic><topic>Depressive Disorder - genetics</topic><topic>Depressive Disorder - physiopathology</topic><topic>Female</topic><topic>Gene loci</topic><topic>Humans</topic><topic>Male</topic><topic>Memory</topic><topic>Mental depression</topic><topic>Middle Aged</topic><topic>Psychosomatic medicine</topic><topic>Scotland</topic><topic>Time Factors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luciano, Michelle</creatorcontrib><creatorcontrib>Pujals, Ana Maria Fernández</creatorcontrib><creatorcontrib>Marioni, Riccardo E</creatorcontrib><creatorcontrib>Campbell, Archie</creatorcontrib><creatorcontrib>Hayward, Caroline</creatorcontrib><creatorcontrib>MacIntyre, Donald J</creatorcontrib><creatorcontrib>Porteous, David J</creatorcontrib><creatorcontrib>McIntosh, Andrew M</creatorcontrib><creatorcontrib>Deary, Ian J</creatorcontrib><creatorcontrib>Generation Scotland Investigators</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Psychosomatic medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luciano, Michelle</au><au>Pujals, Ana Maria Fernández</au><au>Marioni, Riccardo E</au><au>Campbell, Archie</au><au>Hayward, Caroline</au><au>MacIntyre, Donald J</au><au>Porteous, David J</au><au>McIntosh, Andrew M</au><au>Deary, Ian J</au><aucorp>Generation Scotland Investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Current versus lifetime depression, APOE variation, and their interaction on cognitive performance in younger and older adults</atitle><jtitle>Psychosomatic medicine</jtitle><addtitle>Psychosom Med</addtitle><date>2015-06-01</date><risdate>2015</risdate><volume>77</volume><issue>5</issue><spage>480</spage><epage>492</epage><pages>480-492</pages><issn>0033-3174</issn><eissn>1534-7796</eissn><coden>PSMEAP</coden><abstract>An interaction effect of depressive symptoms and APOE e4 allele status on cognitive decline has been shown in old age: e4 allele carriers with more depressive symptoms have faster cognitive decline than those with either depression or the e4 allele. We test this interaction effect on four cognitive domains, using a clinical depression measure comparing current versus lifetime depression.
14,379 individuals aged 18 to 59 years, and 3944 individuals aged 60 to 94 years from the Generation Scotland: Scottish Family Health Study participated. Linear-mixed models-accounting for participant relatedness and demographic and health indices-tested for effects of depression and APOE on cognitive abilities.
There was no interaction between depression and APOE on cognition (p > .05). Current depression was associated with poorer speed (in both groups) and memory (18- to 59-year-olds); differences ranged from 0.01 to 0.03 standard deviation [SD]. For lifetime depression, cognitive performance was lower for digit symbol in younger adults, but higher for vocabulary in both younger (0.03 SD) and older (0.05 SD) adults. A negative effect of the APOE e4 allele on speed and memory was found in the group 60 years and older (effect sizes of 0.04 SD).
The absence of a depression by APOE interaction on cognitive abilities suggests that these synergistic effects only operate at the level of cognitive decline. This implies that it is those biological pathways especially affected by aging that become compromised further by the combined presence of depression and APOE e4 in an individual.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins Ovid Technologies</pub><pmid>26035038</pmid><doi>10.1097/PSY.0000000000000190</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Age differences Aged Aged, 80 and over Aging - physiology Apolipoprotein E4 - genetics Cognition - physiology Cognition Disorders - genetics Cognition Disorders - physiopathology Cognitive ability Depressive Disorder - genetics Depressive Disorder - physiopathology Female Gene loci Humans Male Memory Mental depression Middle Aged Psychosomatic medicine Scotland Time Factors Young Adult |
title | Current versus lifetime depression, APOE variation, and their interaction on cognitive performance in younger and older adults |
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