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Circulating levels of oxytocin may be elevated in complicated grief: a pilot study

Complicated grief (CG) is a debilitating syndrome characterized by persisting and intense distress and impairment after the death of a loved one. The biological mechanisms associated with this syndrome remain unclear but may involve neurobiological pathways implicated in the stress response and atta...

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Autores principales: Bui, Eric, Hellberg, Samantha N., Hoeppner, Susanne S., Rosencrans, Peter, Young, Allison, Ross, Rachel A., Hoge, Elizabeth, Simon, Naomi M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713138/
https://www.ncbi.nlm.nih.gov/pubmed/31489134
http://dx.doi.org/10.1080/20008198.2019.1646603
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author Bui, Eric
Hellberg, Samantha N.
Hoeppner, Susanne S.
Rosencrans, Peter
Young, Allison
Ross, Rachel A.
Hoge, Elizabeth
Simon, Naomi M.
author_facet Bui, Eric
Hellberg, Samantha N.
Hoeppner, Susanne S.
Rosencrans, Peter
Young, Allison
Ross, Rachel A.
Hoge, Elizabeth
Simon, Naomi M.
author_sort Bui, Eric
collection PubMed
description Complicated grief (CG) is a debilitating syndrome characterized by persisting and intense distress and impairment after the death of a loved one. The biological mechanisms associated with this syndrome remain unclear but may involve neurobiological pathways implicated in the stress response and attachment systems. The neuropeptide oxytocin has been implicated in attachment and social behaviour, and loss of social bonds has been associated with disruptions in oxytocin signalling. Furthermore, prior research has reported associations between circulating oxytocin and other mental illnesses, including depression. The present pilot study aimed to examine plasma levels of oxytocin in bereaved adults with primary CG (n = 47) compared to age- and sex-matched bereaved individuals with primary Major Depressive Disorder (MDD) (n = 46), and bereaved individuals without any mental disorder (n = 46). In unadjusted analyses comparing groups according to primary diagnosis, oxytocin levels were significantly higher for primary CG compared to primary MDD (p = 0.013), but not compared to bereaved controls (p = 0.069). In adjusted regression models, having a primary or probable (Inventory of Complicated Grief ≥ 30) diagnosis of CG was associated with significantly higher oxytocin levels (p = 0.001). While additional research is needed, findings from our pilot study provide preliminary support for recent conceptualizations of CG implicating a role for oxytocin and the attachment system. Importantly, these findings contribute to the limited current knowledge about possible biological correlates of CG.
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spelling pubmed-67131382019-09-05 Circulating levels of oxytocin may be elevated in complicated grief: a pilot study Bui, Eric Hellberg, Samantha N. Hoeppner, Susanne S. Rosencrans, Peter Young, Allison Ross, Rachel A. Hoge, Elizabeth Simon, Naomi M. Eur J Psychotraumatol Short Communication Complicated grief (CG) is a debilitating syndrome characterized by persisting and intense distress and impairment after the death of a loved one. The biological mechanisms associated with this syndrome remain unclear but may involve neurobiological pathways implicated in the stress response and attachment systems. The neuropeptide oxytocin has been implicated in attachment and social behaviour, and loss of social bonds has been associated with disruptions in oxytocin signalling. Furthermore, prior research has reported associations between circulating oxytocin and other mental illnesses, including depression. The present pilot study aimed to examine plasma levels of oxytocin in bereaved adults with primary CG (n = 47) compared to age- and sex-matched bereaved individuals with primary Major Depressive Disorder (MDD) (n = 46), and bereaved individuals without any mental disorder (n = 46). In unadjusted analyses comparing groups according to primary diagnosis, oxytocin levels were significantly higher for primary CG compared to primary MDD (p = 0.013), but not compared to bereaved controls (p = 0.069). In adjusted regression models, having a primary or probable (Inventory of Complicated Grief ≥ 30) diagnosis of CG was associated with significantly higher oxytocin levels (p = 0.001). While additional research is needed, findings from our pilot study provide preliminary support for recent conceptualizations of CG implicating a role for oxytocin and the attachment system. Importantly, these findings contribute to the limited current knowledge about possible biological correlates of CG. Taylor & Francis 2019-08-06 /pmc/articles/PMC6713138/ /pubmed/31489134 http://dx.doi.org/10.1080/20008198.2019.1646603 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Bui, Eric
Hellberg, Samantha N.
Hoeppner, Susanne S.
Rosencrans, Peter
Young, Allison
Ross, Rachel A.
Hoge, Elizabeth
Simon, Naomi M.
Circulating levels of oxytocin may be elevated in complicated grief: a pilot study
title Circulating levels of oxytocin may be elevated in complicated grief: a pilot study
title_full Circulating levels of oxytocin may be elevated in complicated grief: a pilot study
title_fullStr Circulating levels of oxytocin may be elevated in complicated grief: a pilot study
title_full_unstemmed Circulating levels of oxytocin may be elevated in complicated grief: a pilot study
title_short Circulating levels of oxytocin may be elevated in complicated grief: a pilot study
title_sort circulating levels of oxytocin may be elevated in complicated grief: a pilot study
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713138/
https://www.ncbi.nlm.nih.gov/pubmed/31489134
http://dx.doi.org/10.1080/20008198.2019.1646603
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