Social isolation, loneliness, and inflammation: A multi-cohort investigation in early and mid-adulthood
Year: 2023
Type: article
Study design: Observational Study
Abstract: Social isolation and loneliness have been associated with poor health and increased risk for mortality, and inflammation might explain this link. We used data from the Danish TRIAGE Study of acutely admitted medical patients (N = 6,144, mean age 60 years), and from two population-representative birth cohorts: the New Zealand Dunedin Longitudinal Study (N = 881, age 45) and the UK Environmental Risk (E-Risk) Longitudinal Twin Study (N = 1448, age 18), to investigate associations of social isolation with three markers of systemic inflammation: C-reactive protein (CRP), interleukin-6 (IL-6), and a newer inflammation marker, soluble urokinase plasminogen activator receptor (suPAR), which is thought to index systemic chronic inflammation. In the TRIAGE Study, socially isolated patients (those living alone) had significantly higher median levels of suPAR (but not CRP or IL-6) compared with patients not living by themselves. Social isolation prospectively measured in childhood was longitudinally associated with higher CRP, IL-6, and suPAR levels in adulthood (at age 45 in the Dunedin Study and age 18 in the E-Risk Study), but only suPAR remained associated after controlling for covariates. Dunedin Study participants who reported loneliness at age 38 or age 45 had elevated suPAR at age 45. In contrast, E-Risk Study participants reporting loneliness at age 18 did not show any elevated markers of inflammation. In conclusion, social isolation was robustly associated with increased inflammation in adulthood, both in medical patients and in the general population. It was associated in particular with systemic chronic inflammation, evident from the consistently stronger associations with suPAR than other inflammation biomarkers.
Source: Brain Behavior and Immunity
Language: English
Subfield: Health
Field: Social Sciences
Domain: Social Sciences
Open Access status: hybrid
Estimated APC paid: $4,480
Funders: University of Otago, South London and Maudsley NHS Foundation Trust, Wellcome Trust, National Institute for Health and Care Research, Department of Health and Social Care, King's College London, Lundbeckfonden, Jacobs Foundation, H. Lundbeck A/S, Medical Research Council, Economic and Social Research Council, National Institute on Aging, National Institute of Child Health and Human Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G1193229881, G1289651063, G1748805038, G1792944704, G2039281854, Duke Population Research Center, G2462977380, G2548308182, Neuropsychological and genomic signatures of violence exposure in childhood, G4036427723, G4154018034, G4184501341, G4312987371, G4919021182, G5701737369, G6637449936, G6671708061, G6790941097, G7274218533, Centre for Society and Mental Health, Midlife Pace of Aging in the Dunedin Study, G7612986051, G8074709457, G8415457339, G8968736666, Duke Claude D. Pepper Older Americans Independence Center, Aging in 1000 healthy midlife adults: Phase 52 of the Dunedin Study, Quantifying Individual Differences in Midlife Structural Brain Integrity Associated with Later AD/ADRD Risk
OpenAlex ID: W4388849789
