Catechol-O-Methyltransferase gene (val158met) polymorphisms and anxious symptoms in early childhood: The roles of hypothalamus-pituitary-adrenal axis reactivity and life stress

•Early childhood cortisol response is associated with COMT val158met polymorphism.•Interaction between val158met and life stress also predicted child anxiety symptoms.•Cortisol response mediated the main-effect of COMT polymorphism on anxiety symptoms.•Val158Met acts as a moderator of early life str...

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Veröffentlicht in:Neuroscience letters 2017-10, Vol.659, p.86-91
Hauptverfasser: Sheikh, Haroon I., Kryski, Katie R., Kotelnikova, Yuliya, Hayden, Elizabeth P., Singh, Shiva M.
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container_title Neuroscience letters
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creator Sheikh, Haroon I.
Kryski, Katie R.
Kotelnikova, Yuliya
Hayden, Elizabeth P.
Singh, Shiva M.
description •Early childhood cortisol response is associated with COMT val158met polymorphism.•Interaction between val158met and life stress also predicted child anxiety symptoms.•Cortisol response mediated the main-effect of COMT polymorphism on anxiety symptoms.•Val158Met acts as a moderator of early life stress’ influence on childhood behaviour. Individual differences in hypothalamus–pituitary–adrenal (HPA) axis reactivity to stress (measured via salivary cortisol) have been widely implicated in the etiology of internalizing problems such as depression and anxiety. Literature suggests that stress during early childhood is an important source of contextual risk although its effects may be moderated by polymorphisms of neurotransmitter genes. The COMT val158met is one such polymorphism, and literature documents its link to internalizing problems. To extend these findings, and to better understand the role of this polymorphism in developmental risk, we investigated links between the val158met polymorphism and early-age cortisol response. Additionally, we investigated whether cortisol reactivity mediated the link between COMT and emerging internalizing symptoms. The study was conducted in a community sample of 409 preschoolers. Saliva samples were collected pre-stress task (baseline) and every 10min post-stress task for one-hour to asses cortisol response. Child anxious and depressive symptoms were tabulated based on parent-reports. Markers of early childhood stress included marital discord, socio-economic status and the UCLA Life Stress Interview. Findings indicated that the val158met polymorphism is associated with childhood cortisol response (p
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Individual differences in hypothalamus–pituitary–adrenal (HPA) axis reactivity to stress (measured via salivary cortisol) have been widely implicated in the etiology of internalizing problems such as depression and anxiety. Literature suggests that stress during early childhood is an important source of contextual risk although its effects may be moderated by polymorphisms of neurotransmitter genes. The COMT val158met is one such polymorphism, and literature documents its link to internalizing problems. To extend these findings, and to better understand the role of this polymorphism in developmental risk, we investigated links between the val158met polymorphism and early-age cortisol response. Additionally, we investigated whether cortisol reactivity mediated the link between COMT and emerging internalizing symptoms. The study was conducted in a community sample of 409 preschoolers. Saliva samples were collected pre-stress task (baseline) and every 10min post-stress task for one-hour to asses cortisol response. Child anxious and depressive symptoms were tabulated based on parent-reports. Markers of early childhood stress included marital discord, socio-economic status and the UCLA Life Stress Interview. Findings indicated that the val158met polymorphism is associated with childhood cortisol response (p&lt;0.05). A gene-environment interaction between val158met and life stress also predicted child anxiety symptoms (p&lt;0.01). Finally, cortisol response mediated the main-effect of val158met on child anxiety symptoms (pathway ps&lt;0.05). Analyses suggest that COMT val158met moderates the influence of early life stress on preschool-age symptoms of anxiety. 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Individual differences in hypothalamus–pituitary–adrenal (HPA) axis reactivity to stress (measured via salivary cortisol) have been widely implicated in the etiology of internalizing problems such as depression and anxiety. Literature suggests that stress during early childhood is an important source of contextual risk although its effects may be moderated by polymorphisms of neurotransmitter genes. The COMT val158met is one such polymorphism, and literature documents its link to internalizing problems. To extend these findings, and to better understand the role of this polymorphism in developmental risk, we investigated links between the val158met polymorphism and early-age cortisol response. Additionally, we investigated whether cortisol reactivity mediated the link between COMT and emerging internalizing symptoms. The study was conducted in a community sample of 409 preschoolers. Saliva samples were collected pre-stress task (baseline) and every 10min post-stress task for one-hour to asses cortisol response. Child anxious and depressive symptoms were tabulated based on parent-reports. Markers of early childhood stress included marital discord, socio-economic status and the UCLA Life Stress Interview. Findings indicated that the val158met polymorphism is associated with childhood cortisol response (p&lt;0.05). A gene-environment interaction between val158met and life stress also predicted child anxiety symptoms (p&lt;0.01). Finally, cortisol response mediated the main-effect of val158met on child anxiety symptoms (pathway ps&lt;0.05). Analyses suggest that COMT val158met moderates the influence of early life stress on preschool-age symptoms of anxiety. Additionally, cortisol reactivity acts as a mechanistic mediator of the main-effect of COMT genotype on child anxious symptoms.</description><subject>Anxiety</subject><subject>Anxiety - genetics</subject><subject>Anxiety - metabolism</subject><subject>Catechol O-Methyltransferase - genetics</subject><subject>Catechol-O-Methyltransferase</subject><subject>Child, Preschool</subject><subject>Cortisol</subject><subject>Depression</subject><subject>Depression - metabolism</subject><subject>Female</subject><subject>Gene-Environment Interaction</subject><subject>Genetic Predisposition to Disease - genetics</subject><subject>Genotype</subject><subject>HPA axis</subject><subject>Humans</subject><subject>Hydrocortisone - metabolism</subject><subject>Hypothalamo-Hypophyseal System - metabolism</subject><subject>Internalizing</subject><subject>Male</subject><subject>Pituitary-Adrenal System - metabolism</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Saliva - metabolism</subject><subject>Stress, Psychological - metabolism</subject><subject>val158met</subject><issn>0304-3940</issn><issn>1872-7972</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1TAQhS0EopfCGyDkZVkk2HF-HBZI1RV_UlE3ZW35OmPiKycOHueqeSseEZdbWLIYjTQ6M0dnPkJec1Zyxtt3x3KG1UMqK8a7ksmStewJ2XHZVUXXd9VTsmOC1YXoa3ZBXiAeGWMNb-rn5KKSsullK3bk114nMGPwxW3xDdK4-RT1jBaiRqA_YAZ6ddKeN3KC9JYuwW9TiMvocEKq5yHXvQsrUtymJYU8dDMFHf1Gzej8MIYwvKd3I9AYPCANlo7bEtKovZ5WLBaXVpd03Ao9RJi1p_reIY2gTXInl7Y_Jt5ZoJgiIL4kz6z2CK8e-yX5_unj3f5LcXP7-ev--qYwoq1SYRtWCytFa1jbHkzVc8EEB5BdI7oBKgONsJpxqKsBbMsrY7q619YcatMNshaX5Op8d4nh5wqY1OTQgPd6hpxX8V60-Ss9Z1lan6UmBsQIVi3RTTmT4kw9sFJHdWalHlgpJlVmldfePDqshwmGf0t_4WTBh7MAcs6Tg6jQOJgNDC6CSWoI7v8OvwGgvqxc</recordid><startdate>20171017</startdate><enddate>20171017</enddate><creator>Sheikh, Haroon I.</creator><creator>Kryski, Katie R.</creator><creator>Kotelnikova, Yuliya</creator><creator>Hayden, Elizabeth P.</creator><creator>Singh, Shiva M.</creator><general>Elsevier B.V</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>7X8</scope></search><sort><creationdate>20171017</creationdate><title>Catechol-O-Methyltransferase gene (val158met) polymorphisms and anxious symptoms in early childhood: The roles of hypothalamus-pituitary-adrenal axis reactivity and life stress</title><author>Sheikh, Haroon I. ; Kryski, Katie R. ; Kotelnikova, Yuliya ; Hayden, Elizabeth P. ; Singh, Shiva M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-f5043f836c066bc2913031ee87537de2ce53fa01e42def612cc749afcb4c7d843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Anxiety</topic><topic>Anxiety - genetics</topic><topic>Anxiety - metabolism</topic><topic>Catechol O-Methyltransferase - genetics</topic><topic>Catechol-O-Methyltransferase</topic><topic>Child, Preschool</topic><topic>Cortisol</topic><topic>Depression</topic><topic>Depression - metabolism</topic><topic>Female</topic><topic>Gene-Environment Interaction</topic><topic>Genetic Predisposition to Disease - genetics</topic><topic>Genotype</topic><topic>HPA axis</topic><topic>Humans</topic><topic>Hydrocortisone - metabolism</topic><topic>Hypothalamo-Hypophyseal System - metabolism</topic><topic>Internalizing</topic><topic>Male</topic><topic>Pituitary-Adrenal System - metabolism</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Saliva - metabolism</topic><topic>Stress, Psychological - metabolism</topic><topic>val158met</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sheikh, Haroon I.</creatorcontrib><creatorcontrib>Kryski, Katie R.</creatorcontrib><creatorcontrib>Kotelnikova, Yuliya</creatorcontrib><creatorcontrib>Hayden, Elizabeth P.</creatorcontrib><creatorcontrib>Singh, Shiva M.</creatorcontrib><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><jtitle>Neuroscience letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sheikh, Haroon I.</au><au>Kryski, Katie R.</au><au>Kotelnikova, Yuliya</au><au>Hayden, Elizabeth P.</au><au>Singh, Shiva M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catechol-O-Methyltransferase gene (val158met) polymorphisms and anxious symptoms in early childhood: The roles of hypothalamus-pituitary-adrenal axis reactivity and life stress</atitle><jtitle>Neuroscience letters</jtitle><addtitle>Neurosci Lett</addtitle><date>2017-10-17</date><risdate>2017</risdate><volume>659</volume><spage>86</spage><epage>91</epage><pages>86-91</pages><issn>0304-3940</issn><eissn>1872-7972</eissn><abstract>•Early childhood cortisol response is associated with COMT val158met polymorphism.•Interaction between val158met and life stress also predicted child anxiety symptoms.•Cortisol response mediated the main-effect of COMT polymorphism on anxiety symptoms.•Val158Met acts as a moderator of early life stress’ influence on childhood behaviour. Individual differences in hypothalamus–pituitary–adrenal (HPA) axis reactivity to stress (measured via salivary cortisol) have been widely implicated in the etiology of internalizing problems such as depression and anxiety. Literature suggests that stress during early childhood is an important source of contextual risk although its effects may be moderated by polymorphisms of neurotransmitter genes. The COMT val158met is one such polymorphism, and literature documents its link to internalizing problems. To extend these findings, and to better understand the role of this polymorphism in developmental risk, we investigated links between the val158met polymorphism and early-age cortisol response. Additionally, we investigated whether cortisol reactivity mediated the link between COMT and emerging internalizing symptoms. The study was conducted in a community sample of 409 preschoolers. Saliva samples were collected pre-stress task (baseline) and every 10min post-stress task for one-hour to asses cortisol response. Child anxious and depressive symptoms were tabulated based on parent-reports. Markers of early childhood stress included marital discord, socio-economic status and the UCLA Life Stress Interview. Findings indicated that the val158met polymorphism is associated with childhood cortisol response (p&lt;0.05). A gene-environment interaction between val158met and life stress also predicted child anxiety symptoms (p&lt;0.01). Finally, cortisol response mediated the main-effect of val158met on child anxiety symptoms (pathway ps&lt;0.05). Analyses suggest that COMT val158met moderates the influence of early life stress on preschool-age symptoms of anxiety. Additionally, cortisol reactivity acts as a mechanistic mediator of the main-effect of COMT genotype on child anxious symptoms.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>28859863</pmid><doi>10.1016/j.neulet.2017.08.060</doi><tpages>6</tpages></addata></record>
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subjects Anxiety
Anxiety - genetics
Anxiety - metabolism
Catechol O-Methyltransferase - genetics
Catechol-O-Methyltransferase
Child, Preschool
Cortisol
Depression
Depression - metabolism
Female
Gene-Environment Interaction
Genetic Predisposition to Disease - genetics
Genotype
HPA axis
Humans
Hydrocortisone - metabolism
Hypothalamo-Hypophyseal System - metabolism
Internalizing
Male
Pituitary-Adrenal System - metabolism
Polymorphism, Single Nucleotide - genetics
Saliva - metabolism
Stress, Psychological - metabolism
val158met
title Catechol-O-Methyltransferase gene (val158met) polymorphisms and anxious symptoms in early childhood: The roles of hypothalamus-pituitary-adrenal axis reactivity and life stress
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