摘要
目的明确脂蛋白相关磷脂酶A2(Lp-PLA2)和高敏C反应蛋白(hs-CRP)是否有助于改善短暂性脑缺血发作(TIA)患者风险分层,提高预后预测能力。方法选择急诊入院的132例TIA患者,分为阳性事件组34例和阴性事件组98例。2组均进行ABCD2评分,0~3分为低危患者46例,4~5分为中危患者70例,6~7分为高危患者16例。检测Lp-PLA2含量、活性及hs-CRP水平。主要结局采用复合终点分析,90d内脑卒中或死亡及与症状相关≥50%大动脉狭窄或有心源性栓子需要抗凝治疗。结果与阴性事件组比较,阳性事件组Lp-PLA2含量和活性明显升高(P〈0.05)。有大动脉硬化者Lp-PLA2含量和活性较无大动脉硬化者明显升高(P〈0.05)。ABCD24~5分[RR=2.18,95%CI:1.26~3.61,P=0.008];ABCD2评分6~7分[RR=3.43,95%CI:1.91~6.39,P=0.001]Lp-PLA2活性〉33μmol/(L·min)[RR=2.73,95%CI:1.04~7.06,P=0.042]是TIA患者复合终点事件的预测因素。结论 Lp-PLA2检测和ABCD2评分法结合可提高TIA患者90d内发生脑卒中或死亡的预测能力。
Objective To study whether lipoprotein-related phospholipase A2 and hs-CRP can improve the risk stratification and outcome in transient ischemic attack(TIA)patients.MethodsOne hundred and thirty-two TIA patients admitted to our hospital were divided into positive event group(n=34)and negative event group(n=98).The patients were scored according to the ABCD2 and further divided into low risk group with 0-3ABCD2 scores(n=46),moderate risk group with 4-5ABCD2 scores(n=70)and high risk group with 6-7ABCD2 scores(n=16).Their serum Lp-PLA2 actiity and hs-CRP level were measured.Their primary outcomes were analyzed by composite endpoint analysis.The incidence of ischemic stroke or death within 90 days was calculated in patients with their conducting artery stenosis≥50% or cardiogenic embolism needing anticoagulation treatment.Results The serum Lp-PLA2 activity was significantly higher in positive event group than in negative event group and in patients with their conducting artery stenosis≥50%than in those with no conducting artery stenosis(P〈0.05).Composite endpoint analysis showed that 4-5ABCD2 scores,6-7ABCD2 scores,and Lp-PLA2activity〉33μmol/(L·min)were the risk factors for composite end events in TIA patients(RR=2.18,95%CI:1.26-3.61,P =0.008;RR =3.43,95%CI:1.91-6.39,P =0.001;RR =2.73,95%CI:1.04-7.06,P=0.042).Conclusion Lp-PLA2 activity in combination with ABCD2 score can predict ischemic stroke and death within 90 days in TIA patients.
出处
《中华老年心脑血管病杂志》
CAS
2015年第4期365-368,共4页
Chinese Journal of Geriatric Heart,Brain and Vessel Diseases
基金
海南省自然科学基金(811217)
海南省重大科技项目(ZDZX2013003)
海南医学院科研培育基金(HY2010-025)