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Inflammation-related epigenetic risk and child and adolescent mental health: A prospective study from pregnancy to middle adolescence
In 785 mother–child (50% male) pairs from a longitudinal epidemiological birth cohort, we investigated associations between inflammation-related epigenetic polygenic risk scores (i-ePGS), environmental exposures, cognitive function, and child and adolescent internalizing and externalizing problems....
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Published in: | Development and psychopathology 2018-08, Vol.30 (3), p.1145-1156 |
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creator | Barker, Edward D. Cecil, Charlotte A. M. Walton, Esther Houtepen, Lotte C. O'Connor, Thomas G. Danese, Andrea Jaffee, Sara R. Jensen, Sarah K. G. Pariante, Carmine McArdle, Wendy Gaunt, Tom R. Relton, Caroline L. Roberts, Susanna |
description | In 785 mother–child (50% male) pairs from a longitudinal epidemiological birth cohort, we investigated associations between inflammation-related epigenetic polygenic risk scores (i-ePGS), environmental exposures, cognitive function, and child and adolescent internalizing and externalizing problems. We examined prenatal and postnatal effects. For externalizing problems, one prenatal effect was found: i-ePGS at birth associated with higher externalizing problems (ages 7–15) indirectly through lower cognitive function (age 7). For internalizing problems, we identified two effects. For a prenatal effect, i-ePGS at birth associated with higher internalizing symptoms via continuity in i-ePGS at age 7. For a postnatal effect, higher postnatal adversity exposure (birth through age 7) associated with higher internalizing problems (ages 7–15) via higher i-ePGS (age 7). Hence, externalizing problems were related mainly to prenatal effects involving lower cognitive function, whereas internalizing problems appeared related to both prenatal and postnatal effects. The present study supports a link between i-ePGS and child and adolescent mental health. |
doi_str_mv | 10.1017/S0954579418000330 |
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M. ; Walton, Esther ; Houtepen, Lotte C. ; O'Connor, Thomas G. ; Danese, Andrea ; Jaffee, Sara R. ; Jensen, Sarah K. G. ; Pariante, Carmine ; McArdle, Wendy ; Gaunt, Tom R. ; Relton, Caroline L. ; Roberts, Susanna</creator><creatorcontrib>Barker, Edward D. ; Cecil, Charlotte A. M. ; Walton, Esther ; Houtepen, Lotte C. ; O'Connor, Thomas G. ; Danese, Andrea ; Jaffee, Sara R. ; Jensen, Sarah K. G. ; Pariante, Carmine ; McArdle, Wendy ; Gaunt, Tom R. ; Relton, Caroline L. ; Roberts, Susanna</creatorcontrib><description>In 785 mother–child (50% male) pairs from a longitudinal epidemiological birth cohort, we investigated associations between inflammation-related epigenetic polygenic risk scores (i-ePGS), environmental exposures, cognitive function, and child and adolescent internalizing and externalizing problems. We examined prenatal and postnatal effects. For externalizing problems, one prenatal effect was found: i-ePGS at birth associated with higher externalizing problems (ages 7–15) indirectly through lower cognitive function (age 7). For internalizing problems, we identified two effects. For a prenatal effect, i-ePGS at birth associated with higher internalizing symptoms via continuity in i-ePGS at age 7. For a postnatal effect, higher postnatal adversity exposure (birth through age 7) associated with higher internalizing problems (ages 7–15) via higher i-ePGS (age 7). Hence, externalizing problems were related mainly to prenatal effects involving lower cognitive function, whereas internalizing problems appeared related to both prenatal and postnatal effects. The present study supports a link between i-ePGS and child and adolescent mental health.</description><identifier>ISSN: 0954-5794</identifier><identifier>EISSN: 1469-2198</identifier><identifier>DOI: 10.1017/S0954579418000330</identifier><identifier>PMID: 30068408</identifier><language>eng</language><publisher>New York, USA: Cambridge University Press</publisher><subject>Adolescence ; Adolescent ; Adolescents ; Age ; Brain research ; Child ; Child & adolescent mental health ; Child Behavior Disorders - etiology ; Child development ; Cognitive ability ; Cytokines ; Deoxyribonucleic acid ; DNA ; DNA methylation ; Epidemiology ; Epigenetics ; Female ; Gene expression ; Humans ; Hypotheses ; Immune system ; Inflammation ; Inflammation - complications ; Laboratories ; Male ; Mental disorders ; Mental Health ; Mental health care ; Pregnancy ; Prospective Studies ; Risk Factors ; Special Issue Articles ; Stress ; Teenagers</subject><ispartof>Development and psychopathology, 2018-08, Vol.30 (3), p.1145-1156</ispartof><rights>Copyright © Cambridge University Press 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-670d341f02cf7759547f772fc87697c20af7d4800491b45ee1169ae1fb44b2c3</citedby><cites>FETCH-LOGICAL-c416t-670d341f02cf7759547f772fc87697c20af7d4800491b45ee1169ae1fb44b2c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2081315861/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2081315861?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,21376,21394,27924,27925,33611,33769,43733,43814,72960,74221,74310</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30068408$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barker, Edward D.</creatorcontrib><creatorcontrib>Cecil, Charlotte A. M.</creatorcontrib><creatorcontrib>Walton, Esther</creatorcontrib><creatorcontrib>Houtepen, Lotte C.</creatorcontrib><creatorcontrib>O'Connor, Thomas G.</creatorcontrib><creatorcontrib>Danese, Andrea</creatorcontrib><creatorcontrib>Jaffee, Sara R.</creatorcontrib><creatorcontrib>Jensen, Sarah K. 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For externalizing problems, one prenatal effect was found: i-ePGS at birth associated with higher externalizing problems (ages 7–15) indirectly through lower cognitive function (age 7). For internalizing problems, we identified two effects. For a prenatal effect, i-ePGS at birth associated with higher internalizing symptoms via continuity in i-ePGS at age 7. For a postnatal effect, higher postnatal adversity exposure (birth through age 7) associated with higher internalizing problems (ages 7–15) via higher i-ePGS (age 7). Hence, externalizing problems were related mainly to prenatal effects involving lower cognitive function, whereas internalizing problems appeared related to both prenatal and postnatal effects. 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For externalizing problems, one prenatal effect was found: i-ePGS at birth associated with higher externalizing problems (ages 7–15) indirectly through lower cognitive function (age 7). For internalizing problems, we identified two effects. For a prenatal effect, i-ePGS at birth associated with higher internalizing symptoms via continuity in i-ePGS at age 7. For a postnatal effect, higher postnatal adversity exposure (birth through age 7) associated with higher internalizing problems (ages 7–15) via higher i-ePGS (age 7). Hence, externalizing problems were related mainly to prenatal effects involving lower cognitive function, whereas internalizing problems appeared related to both prenatal and postnatal effects. 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subjects | Adolescence Adolescent Adolescents Age Brain research Child Child & adolescent mental health Child Behavior Disorders - etiology Child development Cognitive ability Cytokines Deoxyribonucleic acid DNA DNA methylation Epidemiology Epigenetics Female Gene expression Humans Hypotheses Immune system Inflammation Inflammation - complications Laboratories Male Mental disorders Mental Health Mental health care Pregnancy Prospective Studies Risk Factors Special Issue Articles Stress Teenagers |
title | Inflammation-related epigenetic risk and child and adolescent mental health: A prospective study from pregnancy to middle adolescence |
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