Sleep disturbance and longitudinal risk of inflammation: Moderating influences of social integration and social isolation in the Coronary Artery Risk Development in Young Adults (CARDIA) study.
Title | Sleep disturbance and longitudinal risk of inflammation: Moderating influences of social integration and social isolation in the Coronary Artery Risk Development in Young Adults (CARDIA) study. |
Publication Type | Journal Article |
Year of Publication | 2015 |
Authors | Cho HJin, Seeman TE, Kiefe CI, Lauderdale DS, Irwin MR |
Journal | Brain Behav Immun |
Volume | 46 |
Pagination | 319-26 |
Date Published | 2015 May |
ISSN | 1090-2139 |
Keywords | Adult, C-Reactive Protein, Coronary Artery Disease, Female, Humans, Inflammation, Interleukin-6, Longitudinal Studies, Male, Middle Aged, Sleep, Sleep Wake Disorders, Social Behavior, Social Isolation |
Abstract | Both sleep disturbance and social isolation increase the risk for morbidity and mortality. Systemic inflammation is suspected as a potential mechanism of these associations. However, the complex relationships between sleep disturbance, social isolation, and inflammation have not been examined in a population-based longitudinal study. This study examined the longitudinal association between sleep disturbance and systemic inflammation, and the moderating effects of social isolation on this association. The CARDIA study is a population-based longitudinal study conducted in four US cities. Sleep disturbance - i.e., insomnia complaints and short sleep duration - was assessed in 2962 African-American and White adults at baseline (2000-2001, ages 33-45years). Circulating C-reactive protein (CRP) was measured at baseline and follow-up (2005-2006). Interleukin-6 (IL-6) and subjective and objective social isolation (i.e., feelings of social isolation and social network size) were measured at follow-up. Sleep disturbance was a significant predictor of inflammation five years later after full adjustment for covariates (adjusted betas: 0.048, P=0.012 for CRP; 0.047, P=0.017 for IL-6). Further adjustment for baseline CRP revealed that sleep disturbance also impacted the longitudinal change in CRP levels over five years (adjusted beta: 0.044, P=0.013). Subjective social isolation was a significant moderator of this association between sleep disturbance and CRP (adjusted beta 0.131, P=0.002). Sleep disturbance was associated with heightened systemic inflammation in a general population over a five-year follow-up, and this association was significantly stronger in those who reported feelings of social isolation. Clinical interventions targeting sleep disturbances may be a potential avenue for reducing inflammation, particularly in individuals who feel socially isolated. |
DOI | 10.1016/j.bbi.2015.02.023 |
Alternate Journal | Brain Behav. Immun. |
PubMed ID | 25733101 |
PubMed Central ID | PMC4414819 |
Grant List | 01-HC-48048 / HC / NHLBI NIH HHS / United States 5T32MH019925-15 / MH / NIMH NIH HHS / United States N01 HC005187 / HC / NHLBI NIH HHS / United States N01 HC045134 / HC / NHLBI NIH HHS / United States N01 HC045204 / HC / NHLBI NIH HHS / United States N01 HC045205 / HC / NHLBI NIH HHS / United States N01 HC048047 / HC / NHLBI NIH HHS / United States N01 HC048048 / HC / NHLBI NIH HHS / United States N01 HC048050 / HC / NHLBI NIH HHS / United States N01 HC095095 / HC / NHLBI NIH HHS / United States N01-HC-05187 / HC / NHLBI NIH HHS / United States N01-HC-45134 / HC / NHLBI NIH HHS / United States N01-HC-45204 / HC / NHLBI NIH HHS / United States N01-HC-45205 / HC / NHLBI NIH HHS / United States N01-HC-48047 / HC / NHLBI NIH HHS / United States N01-HC-48049 / HC / NHLBI NIH HHS / United States N01-HC-48050 / HC / NHLBI NIH HHS / United States N01-HC-95095 / HC / NHLBI NIH HHS / United States P30 AG028748 / AG / NIA NIH HHS / United States P30-AG028748 / AG / NIA NIH HHS / United States R01 AG034588 / AG / NIA NIH HHS / United States R01-119159 / / PHS HHS / United States R01-AG026364 / AG / NIA NIH HHS / United States R01-AG034588 / AG / NIA NIH HHS / United States R01-HL079955 / HL / NHLBI NIH HHS / United States R01-MH091352 / MH / NIMH NIH HHS / United States T32 MH019925 / MH / NIMH NIH HHS / United States UL1 TR000124 / TR / NCATS NIH HHS / United States UL1 TR000430 / TR / NCATS NIH HHS / United States UL1TR000124 / TR / NCATS NIH HHS / United States |