Key result
Elevated MCP-1 and IL-8 show no independent association with incident CHD after multivariable adjustment.
Cohort (n=2,358)
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OBJECTIVE: The chemokines monocyte chemoattractant protein-1 (MCP-1/CCL2), interleukin-8 (IL-8/CXCL8), and interferon-gamma-inducible protein-10 (IP-10/CXCL10) have been reported to be involved in the development of atherosclerosis and type 2 diabetes. The aim of this study was to assess whether elevated systemic levels of these chemokines precede coronary events. METHODS AND RESULTS: We investigated MCP-1, IL-8, and IP-10 serum levels in a case-cohort design based on data from 381 individuals (294 men, 87 women) with and 1977 individuals (1006 men, 971 women) without incident coronary heart disease (CHD) from the prospective, population-based MONICA/KORA Augsburg study (1984 to 2002). The mean follow-up time was 11.0 years. Baseline concentrations were significantly higher in cases compared with noncases (P < or = 0.001 for all chemokines). MCP-1 and IL-8 remained associated with CHD risk after adjustment for age, sex, and survey with hazard ratios (95% confidence intervals) comparing extreme tertiles of 1.39 (1.05 to 1.84) for MCP-1 and 1.48 (1.10 to 1.99) for IL-8. However, adjustment for further cardiovascular and immunologic risk factors attenuated the observed associations, and they became nonsignificant. CONCLUSIONS: Elevated systemic levels of the chemokines MCP-1, IL-8, and IP-10 precede CHD but do not represent independent risk factors. Thus, the associations are less pronounced than previously shown for type 2 diabetes.
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Herder et al. (2006) conducted a cohort in Incident coronary heart disease (n=2,358). Elevated baseline serum levels of chemokines (MCP-1, IL-8, IP-10) vs. Lowest tertile of chemokine levels / noncases without incident CHD was evaluated on Incident coronary heart disease (CHD) (HR 1.39, 95% CI 1.05-1.84, p=<=0.001). Elevated MCP-1 and IL-8 levels preceded incident CHD, though multivariable adjustment rendered associations nonsignificant.
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