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The association of childhood maltreatment with depression and anxiety is not moderated by the oxytocin receptor gene

BACKGROUND: The oxytocin receptor (OXTR) gene may be involved in resilience or vulnerability towards stress, and hence in the development of stress-related disorders. There are indications that OXTR single nucleotide polymorphisms (SNPs) interact with early life stressors in predicting levels of dep...

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Autores principales: Tollenaar, Marieke S., Molendijk, Marc L., Penninx, Brenda W. J. H., Milaneschi, Yuri, Antypa, Niki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561157/
https://www.ncbi.nlm.nih.gov/pubmed/28353027
http://dx.doi.org/10.1007/s00406-017-0784-z
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author Tollenaar, Marieke S.
Molendijk, Marc L.
Penninx, Brenda W. J. H.
Milaneschi, Yuri
Antypa, Niki
author_facet Tollenaar, Marieke S.
Molendijk, Marc L.
Penninx, Brenda W. J. H.
Milaneschi, Yuri
Antypa, Niki
author_sort Tollenaar, Marieke S.
collection PubMed
description BACKGROUND: The oxytocin receptor (OXTR) gene may be involved in resilience or vulnerability towards stress, and hence in the development of stress-related disorders. There are indications that OXTR single nucleotide polymorphisms (SNPs) interact with early life stressors in predicting levels of depression and anxiety. To replicate and extend these findings, we examined whether three literature-based OXTR SNPs (rs2254298, rs53576, rs2268498) interact with childhood maltreatment in the development of clinically diagnosed depression and anxiety disorders. METHODS: We included 2567 individuals from the Netherlands Study of Depression and Anxiety. This sample consisted of 387 healthy controls, 428 people with a current or past depressive disorder, 243 people with a current or past anxiety disorder, and 1509 people with both lifetime depression and anxiety diagnoses. Childhood maltreatment was measured with both an interview and via self-report. Additional questionnaires measured depression and anxiety sensitivity. RESULTS: Childhood maltreatment was strongly associated with both lifetime depression and anxiety diagnoses, as well as with depression and anxiety sensitivity. However, the OXTR SNPs did not moderate these associations nor had main effects on outcomes. CONCLUSIONS: The three OXTR gene SNPs did not interact with childhood maltreatment in predicting lifetime depression and anxiety diagnoses or sensitivity. This stresses the importance of replication studies with regard to OXTR gene variants in general populations as well as in clearly established clinical samples.
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spelling pubmed-55611572017-08-31 The association of childhood maltreatment with depression and anxiety is not moderated by the oxytocin receptor gene Tollenaar, Marieke S. Molendijk, Marc L. Penninx, Brenda W. J. H. Milaneschi, Yuri Antypa, Niki Eur Arch Psychiatry Clin Neurosci Original Paper BACKGROUND: The oxytocin receptor (OXTR) gene may be involved in resilience or vulnerability towards stress, and hence in the development of stress-related disorders. There are indications that OXTR single nucleotide polymorphisms (SNPs) interact with early life stressors in predicting levels of depression and anxiety. To replicate and extend these findings, we examined whether three literature-based OXTR SNPs (rs2254298, rs53576, rs2268498) interact with childhood maltreatment in the development of clinically diagnosed depression and anxiety disorders. METHODS: We included 2567 individuals from the Netherlands Study of Depression and Anxiety. This sample consisted of 387 healthy controls, 428 people with a current or past depressive disorder, 243 people with a current or past anxiety disorder, and 1509 people with both lifetime depression and anxiety diagnoses. Childhood maltreatment was measured with both an interview and via self-report. Additional questionnaires measured depression and anxiety sensitivity. RESULTS: Childhood maltreatment was strongly associated with both lifetime depression and anxiety diagnoses, as well as with depression and anxiety sensitivity. However, the OXTR SNPs did not moderate these associations nor had main effects on outcomes. CONCLUSIONS: The three OXTR gene SNPs did not interact with childhood maltreatment in predicting lifetime depression and anxiety diagnoses or sensitivity. This stresses the importance of replication studies with regard to OXTR gene variants in general populations as well as in clearly established clinical samples. Springer Berlin Heidelberg 2017-03-28 2017 /pmc/articles/PMC5561157/ /pubmed/28353027 http://dx.doi.org/10.1007/s00406-017-0784-z Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Tollenaar, Marieke S.
Molendijk, Marc L.
Penninx, Brenda W. J. H.
Milaneschi, Yuri
Antypa, Niki
The association of childhood maltreatment with depression and anxiety is not moderated by the oxytocin receptor gene
title The association of childhood maltreatment with depression and anxiety is not moderated by the oxytocin receptor gene
title_full The association of childhood maltreatment with depression and anxiety is not moderated by the oxytocin receptor gene
title_fullStr The association of childhood maltreatment with depression and anxiety is not moderated by the oxytocin receptor gene
title_full_unstemmed The association of childhood maltreatment with depression and anxiety is not moderated by the oxytocin receptor gene
title_short The association of childhood maltreatment with depression and anxiety is not moderated by the oxytocin receptor gene
title_sort association of childhood maltreatment with depression and anxiety is not moderated by the oxytocin receptor gene
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561157/
https://www.ncbi.nlm.nih.gov/pubmed/28353027
http://dx.doi.org/10.1007/s00406-017-0784-z
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