TY - JOUR
T1 - Repeated exposure to systemic inflammation and risk of new depressive symptoms among older adults
AU - MRC Immunopsychiatry Consortium
AU - Bell, J. A.
AU - Kivimäki, M.
AU - Bullmore, E. T.
AU - Steptoe, A.
AU - Carvalho, L. A.
AU - Vértes, Petra E.
AU - Cardinal, Rudolf
AU - Richardson, Sylvia
AU - Leday, Gwenael
AU - Freeman, Tom
AU - Hume, David
AU - Regan, Tim
AU - Wu, Zhaozong
AU - Pariante, Carmine
AU - Cattaneo, Annamaria
AU - Zuszain, Patricia
AU - Borsini, Alessandra
AU - Stewart, Robert
AU - Chandran, David
AU - Souza-Teodoro, Luis Henrique
AU - Perry, Hugh
AU - Harrison, Neil
AU - Janssen, Wayne Drevets
AU - Wittenberg, Gayle M.
AU - Sun, Yu
AU - Jones, Declan
AU - Bullmore, Edward
AU - Khan, Shahid
AU - Stylianou, Annie
AU - Henderson, Robert B.
N1 - Publisher Copyright:
© The Author(s) 2017.
PY - 2017/8/15
Y1 - 2017/8/15
N2 - Evidence on systemic inflammation as a risk factor for future depression is inconsistent, possibly due to a lack of regard for persistency of exposure. We examined whether being inflamed on multiple occasions increases risk of new depressive symptoms using prospective data from a population-based sample of adults aged 50 years or older (the English Longitudinal Study of Ageing). Participants with less than four of eight depressive symptoms in 2004/05 and 2008/09 based on the Eight-item Centre for Epidemiologic Studies Depression scale were analysed. The number of occasions with C-reactive protein ⩾ 3mgl−1 over the same initial assessments (1 vs 0 occasion, and 2 vs 0 occasions) was examined in relation to change in depressive symptoms between 2008/09 and 2012/13 and odds of developing depressive symptomology (having more than or equal to four of eight symptoms) in 2012/13. In multivariable-adjusted regression models (n = 2068), participants who were inflamed on 1 vs 0 occasion showed no increase in depressive symptoms nor raised odds of developing depressive symptomology; those inflamed on 2 vs 0 occasions showed a 0.10 (95% confidence intervals (CIs) = − 0.07, 0.28) symptom increase and 1.60 (95% CI = 1.00, 2.55) times higher odds. In further analyses, 2 vs 0 occasions of inflammation were associated with increased odds of developing depressive symptoms among women (odds ratio (OR) = 2.75, 95% CI = 1.53, 4.95), but not among men (OR = 0.70, 95% CI = 0.29, 1.68); P-for-sex interaction = 0.035. In this cohort study of older adults, repeated but not transient exposure to systemic inflammation was associated with increased risk of future depressive symptoms among women; this subgroup finding requires confirmation of validity.
AB - Evidence on systemic inflammation as a risk factor for future depression is inconsistent, possibly due to a lack of regard for persistency of exposure. We examined whether being inflamed on multiple occasions increases risk of new depressive symptoms using prospective data from a population-based sample of adults aged 50 years or older (the English Longitudinal Study of Ageing). Participants with less than four of eight depressive symptoms in 2004/05 and 2008/09 based on the Eight-item Centre for Epidemiologic Studies Depression scale were analysed. The number of occasions with C-reactive protein ⩾ 3mgl−1 over the same initial assessments (1 vs 0 occasion, and 2 vs 0 occasions) was examined in relation to change in depressive symptoms between 2008/09 and 2012/13 and odds of developing depressive symptomology (having more than or equal to four of eight symptoms) in 2012/13. In multivariable-adjusted regression models (n = 2068), participants who were inflamed on 1 vs 0 occasion showed no increase in depressive symptoms nor raised odds of developing depressive symptomology; those inflamed on 2 vs 0 occasions showed a 0.10 (95% confidence intervals (CIs) = − 0.07, 0.28) symptom increase and 1.60 (95% CI = 1.00, 2.55) times higher odds. In further analyses, 2 vs 0 occasions of inflammation were associated with increased odds of developing depressive symptoms among women (odds ratio (OR) = 2.75, 95% CI = 1.53, 4.95), but not among men (OR = 0.70, 95% CI = 0.29, 1.68); P-for-sex interaction = 0.035. In this cohort study of older adults, repeated but not transient exposure to systemic inflammation was associated with increased risk of future depressive symptoms among women; this subgroup finding requires confirmation of validity.
UR - http://www.scopus.com/inward/record.url?scp=85046072710&partnerID=8YFLogxK
U2 - 10.1038/tp.2017.155
DO - 10.1038/tp.2017.155
M3 - Article
C2 - 28809860
AN - SCOPUS:85046072710
SN - 2158-3188
VL - 7
SP - 1
EP - 8
JO - Translational Psychiatry
JF - Translational Psychiatry
M1 - e1208
ER -