Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/30204
Appears in Collections:Faculty of Health Sciences and Sport Journal Articles
Peer Review Status: Refereed
Title: Depressive symptoms post hip fracture in older adults are associated with phenotypic and functional alterations in T cells
Author(s): Duggal, Niharika Arora
Upton, Jane
Phillips, Anna C
Hampson, Peter
Lord, Janet M
Keywords: Depressive symptoms
Hip fracture
T cell
Stress
Immunity
Inflammation
Ageing
Cortisol
Issue Date: 2014
Citation: Duggal NA, Upton J, Phillips AC, Hampson P & Lord JM (2014) Depressive symptoms post hip fracture in older adults are associated with phenotypic and functional alterations in T cells. Immunity and Ageing, 11 (1), Art. No.: 25. https://doi.org/10.1186/s12979-014-0025-5
Abstract: Background Ageing is accompanied by reduced immunity, termed immunesenescence. The immune system does not act in isolation and is sensitive to both psychological and physical stress. Hip fracture is a common physical stressor in older adults with a high incidence of new onset depression, which relates to poorer prognosis. We therefore set out to examine the possible synergistic effects of physical stress (hip fracture) and psychological stress (depressive symptoms) on the aged immune system. Results T cell phenotype and function was assessed in 101 hip fracture patients (81 female) 6 weeks after hip fracture and 43 healthy age-matched controls (26 female). 38 fracture patients had depressive symptoms at 6 weeks. T cell frequency (p = .01) and numbers (p = .003) were both lower in depressed hip fracture patients compared to healthy controls. The frequency of senescent CD28-ve (p = .001), CD57+ve (p = .001), KLRG1+ve (p = .03) CD8 T cells, as well as senescent CD28-ve CD4+ve (p = .01) and CD57+ve CD4+ve (p = .003) T cells were higher in depressed hip fracture patients compared with healthy controls and the frequency of CD28-ve CD8 T cells was also higher when compared to patients with hip fracture alone (p = .01). Additionally, activated CD69+ve (p = .005) and HLADR+ve (p 
DOI Link: 10.1186/s12979-014-0025-5
Rights: © 2014 Duggal et al.; licensee BioMed Central. 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.
Licence URL(s): http://creativecommons.org/licenses/by/4.0/

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