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Bereavement reduces neutrophil oxidative burst only in older adults: role of the HPA axis and immunesenescence

BACKGROUND: The effect of the chronic stress of bereavement on immunity is poorly understood. Previous studies have demonstrated negative effects on immunity in older adults, and those who report higher depressive symptoms. The aim of the present study was to compare the effect of bereavement on neu...

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Autores principales: Vitlic, Ana, Khanfer, Riyad, Lord, Janet M, Carroll, Douglas, Phillips, Anna C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154898/
https://www.ncbi.nlm.nih.gov/pubmed/25191511
http://dx.doi.org/10.1186/1742-4933-11-13
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author Vitlic, Ana
Khanfer, Riyad
Lord, Janet M
Carroll, Douglas
Phillips, Anna C
author_facet Vitlic, Ana
Khanfer, Riyad
Lord, Janet M
Carroll, Douglas
Phillips, Anna C
author_sort Vitlic, Ana
collection PubMed
description BACKGROUND: The effect of the chronic stress of bereavement on immunity is poorly understood. Previous studies have demonstrated negative effects on immunity in older adults, and those who report higher depressive symptoms. The aim of the present study was to compare the effect of bereavement on neutrophil function in healthy young and old adults, also assessing serum levels of the stress hormones, cortisol and dehydroepiandrosterone sulphate (DHEAS). 41 young (mean age 32 years) and 52 older adults (mean age 72 years), bereaved and non-bereaved, took part in the study. They completed questionnaires on socio-demographic and health behaviour characteristics, as well as psychosocial variables, and provided a blood sample for analysis of neutrophil function (phagocytosis and reactive oxygen species (ROS) production) and stress hormone analysis. RESULTS: Bereaved participants in both age groups reported more symptoms of depression and anxiety than controls and scored moderately highly on bereavement-specific questionnaires for these symptoms. Despite this, young bereaved participants showed robust neutrophil function when compared to age-matched non-bereaved controls, and comparable stress hormone levels, while reduced neutrophil ROS production and raised stress hormone levels (cortisol:DHEAS ratio) were seen in the older bereaved group compared to their age-matched controls. CONCLUSIONS: Reduced neutrophil function among older bereaved participants may be the result of the inability to maintain stress hormone balance, specifically the cortisol:DHEAS ratio.
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spelling pubmed-41548982014-09-05 Bereavement reduces neutrophil oxidative burst only in older adults: role of the HPA axis and immunesenescence Vitlic, Ana Khanfer, Riyad Lord, Janet M Carroll, Douglas Phillips, Anna C Immun Ageing Research BACKGROUND: The effect of the chronic stress of bereavement on immunity is poorly understood. Previous studies have demonstrated negative effects on immunity in older adults, and those who report higher depressive symptoms. The aim of the present study was to compare the effect of bereavement on neutrophil function in healthy young and old adults, also assessing serum levels of the stress hormones, cortisol and dehydroepiandrosterone sulphate (DHEAS). 41 young (mean age 32 years) and 52 older adults (mean age 72 years), bereaved and non-bereaved, took part in the study. They completed questionnaires on socio-demographic and health behaviour characteristics, as well as psychosocial variables, and provided a blood sample for analysis of neutrophil function (phagocytosis and reactive oxygen species (ROS) production) and stress hormone analysis. RESULTS: Bereaved participants in both age groups reported more symptoms of depression and anxiety than controls and scored moderately highly on bereavement-specific questionnaires for these symptoms. Despite this, young bereaved participants showed robust neutrophil function when compared to age-matched non-bereaved controls, and comparable stress hormone levels, while reduced neutrophil ROS production and raised stress hormone levels (cortisol:DHEAS ratio) were seen in the older bereaved group compared to their age-matched controls. CONCLUSIONS: Reduced neutrophil function among older bereaved participants may be the result of the inability to maintain stress hormone balance, specifically the cortisol:DHEAS ratio. BioMed Central 2014-08-29 /pmc/articles/PMC4154898/ /pubmed/25191511 http://dx.doi.org/10.1186/1742-4933-11-13 Text en Copyright © 2014 Vitlic et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Vitlic, Ana
Khanfer, Riyad
Lord, Janet M
Carroll, Douglas
Phillips, Anna C
Bereavement reduces neutrophil oxidative burst only in older adults: role of the HPA axis and immunesenescence
title Bereavement reduces neutrophil oxidative burst only in older adults: role of the HPA axis and immunesenescence
title_full Bereavement reduces neutrophil oxidative burst only in older adults: role of the HPA axis and immunesenescence
title_fullStr Bereavement reduces neutrophil oxidative burst only in older adults: role of the HPA axis and immunesenescence
title_full_unstemmed Bereavement reduces neutrophil oxidative burst only in older adults: role of the HPA axis and immunesenescence
title_short Bereavement reduces neutrophil oxidative burst only in older adults: role of the HPA axis and immunesenescence
title_sort bereavement reduces neutrophil oxidative burst only in older adults: role of the hpa axis and immunesenescence
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154898/
https://www.ncbi.nlm.nih.gov/pubmed/25191511
http://dx.doi.org/10.1186/1742-4933-11-13
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