Neuropsychological deficits in major depression reflect genetic/familial risk more than clinical history: A monozygotic discordant twin-pair study
Abstract Neuropsychological deficits have been associated with major depression (MD) and persist in some individuals even after symptom remission. However, it is unclear if the deficits are a consequence of MD or are pre-existing and reflect MD vulnerability. We addressed this issue by studying 117...
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description | Abstract Neuropsychological deficits have been associated with major depression (MD) and persist in some individuals even after symptom remission. However, it is unclear if the deficits are a consequence of MD or are pre-existing and reflect MD vulnerability. We addressed this issue by studying 117 twins from monozygotic (MZ) pairs discordant for lifetime history of DSM-III-R defined MD and 41 twins from MZ pairs in which neither twin had experienced MD. Our assessment included a structured clinical interview and measures from the WMS-III and WAIS-III. The “unaffected” twins from discordant pairs showed the same pattern of performance as their affected cotwins on measures of attention, working memory, verbal memory, and visuo-spatial processing. Compared to twins from pairs with no MD history, twins in discordant pairs had lower performance in the domains of attention, memory, visuo-spatial processing, and general knowledge. However, after adjusting for sex and age, the groups differed only on attention and general knowledge. The similar performance of twins in pairs discordant for MD suggests that familial risk for MD has a greater influence on neuropsychological functioning than individual MD history. Findings of impairment in individuals euthymic for MD are more consistent with pre-existing deficits than scarring effects of MD. |
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However, it is unclear if the deficits are a consequence of MD or are pre-existing and reflect MD vulnerability. We addressed this issue by studying 117 twins from monozygotic (MZ) pairs discordant for lifetime history of DSM-III-R defined MD and 41 twins from MZ pairs in which neither twin had experienced MD. Our assessment included a structured clinical interview and measures from the WMS-III and WAIS-III. The “unaffected” twins from discordant pairs showed the same pattern of performance as their affected cotwins on measures of attention, working memory, verbal memory, and visuo-spatial processing. Compared to twins from pairs with no MD history, twins in discordant pairs had lower performance in the domains of attention, memory, visuo-spatial processing, and general knowledge. However, after adjusting for sex and age, the groups differed only on attention and general knowledge. The similar performance of twins in pairs discordant for MD suggests that familial risk for MD has a greater influence on neuropsychological functioning than individual MD history. Findings of impairment in individuals euthymic for MD are more consistent with pre-existing deficits than scarring effects of MD.</description><identifier>ISSN: 0165-1781</identifier><identifier>EISSN: 1872-7123</identifier><identifier>DOI: 10.1016/j.psychres.2013.10.037</identifier><identifier>PMID: 24262663</identifier><identifier>CODEN: PSRSDR</identifier><language>eng</language><publisher>Kidlington: Elsevier Ireland Ltd</publisher><subject>Adult ; Adult and adolescent clinical studies ; Attention ; Biological and medical sciences ; Cognitive functioning ; Depression ; Depressive Disorder, Major - genetics ; Depressive Disorder, Major - psychology ; Diseases in Twins - genetics ; Diseases in Twins - psychology ; Female ; Genetics ; Humans ; Longitudinal Studies ; Major depression ; Male ; Medical sciences ; Memory ; Middle Aged ; Miscellaneous ; Mood disorders ; Neuropsychological impairment ; Neuropsychological Tests ; Psychiatry ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Risk Factors ; Scarring effects ; Set (Psychology) ; Severity of Illness Index ; Twins ; Twins, Monozygotic - genetics ; Twins, Monozygotic - psychology ; Vocabulary</subject><ispartof>Psychiatry research, 2014-01, Vol.215 (1), p.87-94</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2013 Elsevier Ireland Ltd</rights><rights>2015 INIST-CNRS</rights><rights>2013 Published by Elsevier Ireland Ltd.</rights><rights>2013 Elsevier Ireland Ltd. All rights reserved. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c556t-e80b694ca6de302a4758c6f20d967decddfdd234469d98a1b34a11aeb6e2209b3</citedby><cites>FETCH-LOGICAL-c556t-e80b694ca6de302a4758c6f20d967decddfdd234469d98a1b34a11aeb6e2209b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.psychres.2013.10.037$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,778,782,883,3539,27907,27908,45978</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28163244$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24262663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hsu, Kean J</creatorcontrib><creatorcontrib>Young-Wolff, Kelly C</creatorcontrib><creatorcontrib>Kendler, Kenneth S</creatorcontrib><creatorcontrib>Halberstadt, Lisa J</creatorcontrib><creatorcontrib>Prescott, Carol A</creatorcontrib><title>Neuropsychological deficits in major depression reflect genetic/familial risk more than clinical history: A monozygotic discordant twin-pair study</title><title>Psychiatry research</title><addtitle>Psychiatry Res</addtitle><description>Abstract Neuropsychological deficits have been associated with major depression (MD) and persist in some individuals even after symptom remission. However, it is unclear if the deficits are a consequence of MD or are pre-existing and reflect MD vulnerability. We addressed this issue by studying 117 twins from monozygotic (MZ) pairs discordant for lifetime history of DSM-III-R defined MD and 41 twins from MZ pairs in which neither twin had experienced MD. Our assessment included a structured clinical interview and measures from the WMS-III and WAIS-III. The “unaffected” twins from discordant pairs showed the same pattern of performance as their affected cotwins on measures of attention, working memory, verbal memory, and visuo-spatial processing. Compared to twins from pairs with no MD history, twins in discordant pairs had lower performance in the domains of attention, memory, visuo-spatial processing, and general knowledge. However, after adjusting for sex and age, the groups differed only on attention and general knowledge. The similar performance of twins in pairs discordant for MD suggests that familial risk for MD has a greater influence on neuropsychological functioning than individual MD history. Findings of impairment in individuals euthymic for MD are more consistent with pre-existing deficits than scarring effects of MD.</description><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Attention</subject><subject>Biological and medical sciences</subject><subject>Cognitive functioning</subject><subject>Depression</subject><subject>Depressive Disorder, Major - genetics</subject><subject>Depressive Disorder, Major - psychology</subject><subject>Diseases in Twins - genetics</subject><subject>Diseases in Twins - psychology</subject><subject>Female</subject><subject>Genetics</subject><subject>Humans</subject><subject>Longitudinal Studies</subject><subject>Major depression</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Memory</subject><subject>Middle Aged</subject><subject>Miscellaneous</subject><subject>Mood disorders</subject><subject>Neuropsychological impairment</subject><subject>Neuropsychological Tests</subject><subject>Psychiatry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Risk Factors</subject><subject>Scarring effects</subject><subject>Set (Psychology)</subject><subject>Severity of Illness Index</subject><subject>Twins</subject><subject>Twins, Monozygotic - genetics</subject><subject>Twins, Monozygotic - psychology</subject><subject>Vocabulary</subject><issn>0165-1781</issn><issn>1872-7123</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk1v1DAQhiMEokvhL1S-IHHJ1h-JE3OoqCq-pAoOwNny2pNdbxN7sZ1W4Wfwi3G6u-XjwsnSzDvvjOeZojgjeEkw4efb5S5OehMgLikmLAeXmDWPigVpG1o2hLLHxSIL65I0LTkpnsW4xRhTIsTT4oRWlFPO2aL4-QnG4O-9fO_XVqseGeistiki69Cgtj7kyC53itY7FKDrQSe0BgfJ6vNODba3uSrYeIMGHwCljXJI99bdu21sTD5Mr9Flzjr_Y1r7XIeMjdoHo1xC6c66cqdsQDGNZnpePOlUH-HF4T0tvr17-_XqQ3n9-f3Hq8vrUtc1TyW0eMVFpRU3wDBVVVO3mncUG8EbA9qYzhjKqooLI1pFVqxShChYcaAUixU7LS72vrtxNYDR4FJQvdwFO6gwSa-s_Dvj7Eau_a1koq4bRrPBq4NB8N9HiEkO-VPQ98qBH6MklaBcCNpUWcr3Uh18jHmHD20IljNQuZVHoHIGOscz0Fx49ueQD2VHglnw8iBQMa-7C8ppG3_rWsIZreYJ3ux1kFd6ayHIqC04DcaGzFMab_8_y8U_FkfINzBB3PoxuAxMEhmpxPLLfH7z9RGGMW_biv0CSFrdYA</recordid><startdate>20140130</startdate><enddate>20140130</enddate><creator>Hsu, Kean J</creator><creator>Young-Wolff, Kelly C</creator><creator>Kendler, Kenneth S</creator><creator>Halberstadt, Lisa J</creator><creator>Prescott, Carol A</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140130</creationdate><title>Neuropsychological deficits in major depression reflect genetic/familial risk more than clinical history: A monozygotic discordant twin-pair study</title><author>Hsu, Kean J ; Young-Wolff, Kelly C ; Kendler, Kenneth S ; Halberstadt, Lisa J ; Prescott, Carol A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c556t-e80b694ca6de302a4758c6f20d967decddfdd234469d98a1b34a11aeb6e2209b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Attention</topic><topic>Biological and medical sciences</topic><topic>Cognitive functioning</topic><topic>Depression</topic><topic>Depressive Disorder, Major - genetics</topic><topic>Depressive Disorder, Major - psychology</topic><topic>Diseases in Twins - genetics</topic><topic>Diseases in Twins - psychology</topic><topic>Female</topic><topic>Genetics</topic><topic>Humans</topic><topic>Longitudinal Studies</topic><topic>Major depression</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Memory</topic><topic>Middle Aged</topic><topic>Miscellaneous</topic><topic>Mood disorders</topic><topic>Neuropsychological impairment</topic><topic>Neuropsychological Tests</topic><topic>Psychiatry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Risk Factors</topic><topic>Scarring effects</topic><topic>Set (Psychology)</topic><topic>Severity of Illness Index</topic><topic>Twins</topic><topic>Twins, Monozygotic - genetics</topic><topic>Twins, Monozygotic - psychology</topic><topic>Vocabulary</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hsu, Kean J</creatorcontrib><creatorcontrib>Young-Wolff, Kelly C</creatorcontrib><creatorcontrib>Kendler, Kenneth S</creatorcontrib><creatorcontrib>Halberstadt, Lisa J</creatorcontrib><creatorcontrib>Prescott, Carol A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Psychiatry research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hsu, Kean J</au><au>Young-Wolff, Kelly C</au><au>Kendler, Kenneth S</au><au>Halberstadt, Lisa J</au><au>Prescott, Carol A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuropsychological deficits in major depression reflect genetic/familial risk more than clinical history: A monozygotic discordant twin-pair study</atitle><jtitle>Psychiatry research</jtitle><addtitle>Psychiatry Res</addtitle><date>2014-01-30</date><risdate>2014</risdate><volume>215</volume><issue>1</issue><spage>87</spage><epage>94</epage><pages>87-94</pages><issn>0165-1781</issn><eissn>1872-7123</eissn><coden>PSRSDR</coden><abstract>Abstract Neuropsychological deficits have been associated with major depression (MD) and persist in some individuals even after symptom remission. However, it is unclear if the deficits are a consequence of MD or are pre-existing and reflect MD vulnerability. We addressed this issue by studying 117 twins from monozygotic (MZ) pairs discordant for lifetime history of DSM-III-R defined MD and 41 twins from MZ pairs in which neither twin had experienced MD. Our assessment included a structured clinical interview and measures from the WMS-III and WAIS-III. The “unaffected” twins from discordant pairs showed the same pattern of performance as their affected cotwins on measures of attention, working memory, verbal memory, and visuo-spatial processing. Compared to twins from pairs with no MD history, twins in discordant pairs had lower performance in the domains of attention, memory, visuo-spatial processing, and general knowledge. However, after adjusting for sex and age, the groups differed only on attention and general knowledge. The similar performance of twins in pairs discordant for MD suggests that familial risk for MD has a greater influence on neuropsychological functioning than individual MD history. Findings of impairment in individuals euthymic for MD are more consistent with pre-existing deficits than scarring effects of MD.</abstract><cop>Kidlington</cop><pub>Elsevier Ireland Ltd</pub><pmid>24262663</pmid><doi>10.1016/j.psychres.2013.10.037</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Adult and adolescent clinical studies Attention Biological and medical sciences Cognitive functioning Depression Depressive Disorder, Major - genetics Depressive Disorder, Major - psychology Diseases in Twins - genetics Diseases in Twins - psychology Female Genetics Humans Longitudinal Studies Major depression Male Medical sciences Memory Middle Aged Miscellaneous Mood disorders Neuropsychological impairment Neuropsychological Tests Psychiatry Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Risk Factors Scarring effects Set (Psychology) Severity of Illness Index Twins Twins, Monozygotic - genetics Twins, Monozygotic - psychology Vocabulary |
title | Neuropsychological deficits in major depression reflect genetic/familial risk more than clinical history: A monozygotic discordant twin-pair study |
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