Huang Xiao-Yun, Fu Wen-Jin, Chen Zhi-Chang, Mei Zhi-Zhong, Yu Ying-Li, Fang Hao-Wei, Huang Yi-Hong, Lin Han, Chen Jian-Jun, Wang Ming-Xia, Guan Shao-Bing, Lu Wan-Xian, Chen Xiao-Ling
Department of Neurology, The Affiliated Houjie Hospital, Guangdong Medical University, PR China.
Department of Laboratory, The Affiliated Houjie Hospital, Guangdong Medical University, PR China.
J Clin Neurosci. 2017 Nov;45:265-269. doi: 10.1016/j.jocn.2017.08.004. Epub 2017 Sep 13.
This case-control study was designed to establish a new risk-prediction model for primary stroke using Framingham stroke profile (FSP), cerebral vascular hemodynamic indexes (CVHI) and plasma inflammatory cytokines including hs-CRP, IL-6, TNF-α and Lp-PLA2. A total of 101 primary stroke patients admitted to Dongguan Houjie Hospital between August 2014 and June 2015 were assigned into the case group, and 156 age- and gender-matched healthy subjects from the Houjie Community were allocated into the control group. The prognostic values of FSP, CVHI and inflammatory cytokines including high sensitive C-reactive protein (hs-CRP), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α) and lipoprotein-associated phospholipase A2 (Lp-PLA2) were assessed by multivariate logistic regression analysis. Seven risk-prediction models (FSP, CVHI, inflammatory cytokine, FSP+CVHI, FSP+inflammatory cytokine, CVHI+inflammatory cytokine, CVHI+FSP+inflammatory cytokine) were successfully established and the prognostic values were statistically compared by ROC curve and Z test. For FSP, the stroke risk was significantly elevated by 2.85 times when the FSP score was increased by 1 level (P=0.043), increased by 3.25 times for CVHI (P=0.036), 6.53 times for IL-6 (P=0.003), and 7.75 times for Lp-PLA2 (P=0.000). The sensitivity of FSP+CVHI+inflammatory cytokine and CVHI+inflammatory cytokine models was higher than 90%. For model specificity, the specificity of FSP+CVHI+inflammatory cytokine model alone exceeded 90%. FSP, CVHI, IL-6 and Lp-PLA2 are independent risk factors of stroke. Integrating IL-6 and Lp-PLA2 into the models can significantly enhance the risk prediction accuracy of primary stroke. Combined application of FSP+CVHI+inflammatory cytokine is of potential for risk prediction of primary stroke.
本病例对照研究旨在利用弗雷明汉卒中量表(FSP)、脑血管血流动力学指标(CVHI)以及包括超敏C反应蛋白(hs-CRP)、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)和脂蛋白相关磷脂酶A2(Lp-PLA2)在内的血浆炎症细胞因子建立一种新的原发性卒中风险预测模型。2014年8月至2015年6月期间入住东莞厚街医院的101例原发性卒中患者被纳入病例组,156例来自厚街社区的年龄和性别匹配的健康受试者被分配到对照组。通过多因素逻辑回归分析评估FSP、CVHI以及包括高敏C反应蛋白(hs-CRP)、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)和脂蛋白相关磷脂酶A2(Lp-PLA2)在内的炎症细胞因子的预后价值。成功建立了7种风险预测模型(FSP、CVHI、炎症细胞因子、FSP+CVHI、FSP+炎症细胞因子、CVHI+炎症细胞因子、CVHI+FSP+炎症细胞因子),并通过ROC曲线和Z检验对其预后价值进行统计学比较。对于FSP,当FSP评分升高1个等级时,卒中风险显著升高2.85倍(P=0.043);CVHI升高3.25倍(P=0.036);IL-6升高6.53倍(P=0.003);Lp-PLA2升高7.75倍(P=0.000)。FSP+CVHI+炎症细胞因子模型和CVHI+炎症细胞因子模型的敏感性高于90%。就模型特异性而言,仅FSP+CVHI+炎症细胞因子模型的特异性超过90%。FSP、CVHI、IL-6和Lp-PLA2是卒中的独立危险因素。将IL-6和Lp-PLA2纳入模型可显著提高原发性卒中的风险预测准确性。联合应用FSP+CVHI+炎症细胞因子对原发性卒中具有风险预测潜力。