PMID- 16441967 OWN - NLM STAT- MEDLINE DCOM- 20061213 LR - 20220317 IS - 0021-9320 (Print) IS - 0021-9320 (Linking) VI - 38 IP - 6 DP - 2006 Nov TI - Social networks and inflammatory markers in the Framingham Heart Study. PG - 835-42 AB - Lack of social integration predicts coronary heart disease mortality in prospective studies; however, the biological pathways that may be responsible are poorly understood. The specific aims of this study were to examine whether social networks are associated with serum concentrations of the inflammatory markers interleukin-6 (IL-6), C-reactive protein (CRP), soluble intercellular adhesion molecule-1 (sICAM-1) and monocyte chemoattractant protein-1 (MCP-1). Participants in the Framingham Study attending examinations from 1998 to 2001 (n=3267) were eligible for inclusion in the study. Social networks were assessed using the Berkman-Syme Social Network Index (SNI). Concentrations of IL-6, CRP, sICAM-1 and MCP-1 were measured in fasting serum samples. Multivariable linear regression analyses were used to assess the association of social networks with inflammatory markers adjusting for potential confounders including age, smoking, blood pressure, total:HDL cholesterol ratio, body mass index, lipid-lowering and antihypertensive medication, diabetes, cardiovascular disease, depression and socioeconomic status. Results found that the SNI was significantly inversely associated with IL-6 in men (p=0.03) after adjusting for potential confounders. In age-adjusted analyses, social networks also were significantly inversely associated with IL-6 for women (p=0.03) and were marginally to modestly associated with CRP and sICAM-1 for men (p=0.08 and 0.02, respectively), but these associations were not significant in the multivariate analyses. In conclusion, social networks were found to be inversely associated with interleukin-6 levels in men. The possibility that inflammatory markers may be potential mediators between social integration and coronary heart disease merits further investigation. FAU - Loucks, Eric B AU - Loucks EB AD - Department of Society, Human Development & Health, Harvard School of Public Health, Boston, MA, USA. FAU - Sullivan, Lisa M AU - Sullivan LM FAU - D'Agostino, Ralph B Sr AU - D'Agostino RB Sr FAU - Larson, Martin G AU - Larson MG FAU - Berkman, Lisa F AU - Berkman LF FAU - Benjamin, Emelia J AU - Benjamin EJ LA - eng GR - HL64753/HL/NHLBI NIH HHS/United States GR - HL76784/HL/NHLBI NIH HHS/United States GR - N01-HC-25195/HC/NHLBI NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't DEP - 20060127 PL - England TA - J Biosoc Sci JT - Journal of biosocial science JID - 0177346 RN - 0 (Biomarkers) RN - 0 (Chemokine CCL2) RN - 0 (Interleukin-6) RN - 126547-89-5 (Intercellular Adhesion Molecule-1) RN - 9007-41-4 (C-Reactive Protein) SB - IM MH - Biomarkers MH - C-Reactive Protein/metabolism MH - Chemokine CCL2/blood MH - Coronary Disease/*blood/epidemiology/*psychology MH - Female MH - Humans MH - Inflammation/*blood MH - Intercellular Adhesion Molecule-1/blood MH - Interleukin-6/blood MH - *Interpersonal Relations MH - Linear Models MH - Male MH - Middle Aged MH - Multivariate Analysis MH - *Social Support MH - United States/epidemiology EDAT- 2006/01/31 09:00 MHDA- 2006/12/14 09:00 CRDT- 2006/01/31 09:00 PHST- 2006/01/31 09:00 [pubmed] PHST- 2006/12/14 09:00 [medline] PHST- 2006/01/31 09:00 [entrez] AID - S0021932005001203 [pii] AID - 10.1017/S0021932005001203 [doi] PST - ppublish SO - J Biosoc Sci. 2006 Nov;38(6):835-42. doi: 10.1017/S0021932005001203. Epub 2006 Jan 27.