Neighborhood social cohesion is associated with lower levels of interleukin-6 in African American women.
Adult
Black or African American
/ psychology
Biomarkers
C-Reactive Protein
/ metabolism
Cohort Studies
Female
Friends
/ psychology
Health Status Disparities
Humans
Inflammation
/ metabolism
Interleukin-6
/ analysis
Interpersonal Relations
Male
Middle Aged
Residence Characteristics
Risk Factors
Sex Factors
Social Behavior
White People
Inflammation
Intersectionality
Neighborhood
Social cohesion
Journal
Brain, behavior, and immunity
ISSN: 1090-2139
Titre abrégé: Brain Behav Immun
Pays: Netherlands
ID NLM: 8800478
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
23
04
2018
revised:
30
08
2018
accepted:
23
10
2018
entrez:
29
1
2019
pubmed:
29
1
2019
medline:
29
2
2020
Statut:
ppublish
Résumé
Social cohesion is a positive neighborhood characteristic defined by feelings of connectedness and solidarity within a community. Studies have found significant associations between social cohesion and cardiovascular disease (CVD) risk factors and outcomes. Inflammation is one potential physiological pathway linking social cohesion to CVD development, but few studies have evaluated the relationship between social cohesion and inflammatory biomarkers. Prior research has also established that race and gender can modify the effects of neighborhood features, including social cohesion, on CVD risk factors and outcomes. This study aimed to examine the association between social cohesion and the inflammatory biomarkers interleukin-6 (IL-6) and C-reactive protein (CRP) in a cohort of African American and White women and men. Data from the Morehouse and Emory Team Up to Eliminate Health Disparities (META-Health) Study were used to assess the association between social cohesion and inflammation among African American (n = 203) and White (n = 176) adults from the Atlanta metropolitan area. Social cohesion was measured using the social cohesion subscale from the Neighborhood Health Questionnaire. Inflammatory biomarkers were measured from plasma frozen at -70 °C. Multivariable linear regression analyses were conducted, controlling for demographic, clinical, behavioral, and psychosocial factors sequentially. Interaction by race and gender was also examined. In models adjusted for age, race, gender, and education, social cohesion was significantly associated with lower levels of IL-6 (β = -0.06, p = 0.03). There was a significant race × social cohesion interaction (p = 0.04), and a marginally significant gender × race × social cohesion interaction (p = 0.09). In race-stratified models controlling for age, gender, and education, social cohesion was associated with lower IL-6 levels in African Americans (β = -0.11, p = 0.01), but not Whites (β = 0.01, p = 0.91). In fully adjusted race- and gender-stratified models, social cohesion was associated with lower levels of IL-6 in African American women only (β = -0.15, p = 0.003). CRP was not associated with social cohesion in fully adjusted models. The association between social cohesion and lower levels of IL-6 is modified by gender and race, with the strongest association emerging for African American women. Although the pathways through which social cohesion impacts inflammation remain unclear, it is possible that for African American women social cohesion manifests through neighborhood networks.
Identifiants
pubmed: 30686334
pii: S0889-1591(18)30740-2
doi: 10.1016/j.bbi.2018.10.008
pmc: PMC6370481
mid: NIHMS1511565
pii:
doi:
Substances chimiques
Biomarkers
0
Interleukin-6
0
C-Reactive Protein
9007-41-4
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
28-36Subventions
Organisme : NIAID NIH HHS
ID : R38 AI140299
Pays : United States
Organisme : NCRR NIH HHS
ID : U54 RR022814
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL130471
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL130025
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL079214
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL079156
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR070898
Pays : United States
Organisme : NICHD NIH HHS
ID : K12 HD085850
Pays : United States
Organisme : NIA NIH HHS
ID : U54 AG062334
Pays : United States
Informations de copyright
Copyright © 2018 Elsevier Inc. All rights reserved.
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