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.

TitleSleep 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 TypeJournal Article
Year of Publication2015
AuthorsCho HJin, Seeman TE, Kiefe CI, Lauderdale DS, Irwin MR
JournalBrain Behav Immun
Volume46
Pagination319-26
Date Published2015 May
ISSN1090-2139
KeywordsAdult, 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.

DOI10.1016/j.bbi.2015.02.023
Alternate JournalBrain Behav. Immun.
PubMed ID25733101
PubMed Central IDPMC4414819
Grant List01-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