University of Glasgow, Scotland, UK.
Cytokine. 2010 Apr;50(1):94-8. doi: 10.1016/j.cyto.2009.12.014. Epub 2010 Jan 21.
The pro-inflammatory cytokines, interleukin (IL)-18 and tumour necrosis factor-alpha (TNFalpha) may play a role in coronary heart disease (CHD). We aimed to extend data on their relationships to the risk of CHD in generally healthy populations.
During 5.5years follow-up in the Fletcher Challenge general population cohort there were 256 CHD cases, and 615 controls were matched for age and sex. Baseline plasma levels of IL-18 and TNFalpha were related to CHD risk in available samples (77%).
Plasma levels of IL-18 (11% increase in mean, p=0.01) and TNFalpha (10% increase in mean p=0.024) were significantly elevated in CHD cases versus controls. In univariable models IL-18 was associated with CHD risk (odds ratio [OR] upper third to lower third, 1.63; 95% CI 1.08, 2.46), but TNFalpha was not (OR 1.33; 95% CI 0.87, 2.02).After adjusting for major CHD risk factors and CRP, the association of IL-18 with CHD risk was attenuated (OR 1.69; 95% CI 0.94, 3.03).
IL-18, but not TNFalpha, had a non-negligible association with CHD risk, although the association of IL-18 with risk was weak after full adjustment. These cytokines may play a role in CHD pathology, but may not be robust risk biomarkers.
促炎细胞因子白细胞介素(IL)-18 和肿瘤坏死因子-α(TNFalpha)可能在冠心病(CHD)中发挥作用。我们旨在扩展其与一般健康人群中 CHD 风险关系的数据。
在弗莱彻挑战普通人群队列中进行了 5.5 年的随访,有 256 例 CHD 病例,615 例对照按年龄和性别匹配。在可获得的样本中(77%),基线血浆中 IL-18 和 TNFalpha 的水平与 CHD 风险相关。
CHD 病例与对照组相比,血浆中 IL-18(平均升高 11%,p=0.01)和 TNFalpha(平均升高 10%,p=0.024)水平显著升高。在单变量模型中,IL-18 与 CHD 风险相关(上三分之一与下三分之一的比值比 [OR],1.63;95%置信区间 [CI],1.08,2.46),而 TNFalpha 则不然(OR 1.33;95% CI,0.87,2.02)。在调整主要 CHD 危险因素和 CRP 后,IL-18 与 CHD 风险的相关性减弱(OR 1.69;95% CI,0.94,3.03)。
IL-18 而非 TNFalpha 与 CHD 风险有一定的关联,尽管在充分调整后,IL-18 与风险的关联较弱。这些细胞因子可能在 CHD 病理中发挥作用,但不是稳健的风险生物标志物。