中国医学影像学杂志
中國醫學影像學雜誌
중국의학영상학잡지
Chinese Journal of Medical Imaging
2015年
9期
659-662
,共4页
许寅宏%徐恩%林清原%邱少东
許寅宏%徐恩%林清原%邱少東
허인굉%서은%림청원%구소동
卒中%脑缺血%急性病%脂蛋白类,LDL%超声检查,多普勒,彩色%颈动脉%动脉硬化
卒中%腦缺血%急性病%脂蛋白類,LDL%超聲檢查,多普勒,綵色%頸動脈%動脈硬化
졸중%뇌결혈%급성병%지단백류,LDL%초성검사,다보륵,채색%경동맥%동맥경화
Stroke%Brain ischemia%Acute disease%Lipoproteins,LDL%Ultrasonography,Doppler,color%Carotid arteries%Arteriosclerosis
目的:探讨急性缺血性脑卒中患者血清氧化型低密度脂蛋白(ox-LDL)水平与颈动脉易损斑块的关系,评估ox-LDL对易损性颈动脉斑块的识别能力,为早期识别易损性颈动脉斑块探索新的途径。资料与方法选择经CT和MRI确诊为急性缺血性脑卒中的181例患者,根据颈动脉超声检查将其分为无斑块组48例、稳定斑块组38例、易损斑块组95例。检测血清总胆固醇、三酰甘油、高密度脂蛋白胆固醇、低密度脂蛋白胆固醇、空腹血糖及血清ox-LDL水平,并采用双功能彩色多普勒超声检测颈动脉内膜中层厚度(IMT)、总斑块面积(TPA)及斑块性质,分析血清ox-LDL与缺血性脑卒中危险因素的相关性。结果斑块组合并高血压、血清ox-LDL明显高于无斑块组(P<0.05);易损斑块组血清ox-LDL、TPA明显高于稳定斑块组(P<0.01)。血清ox-LDL水平与颈动脉IMT、总胆固醇、LDL-C呈正相关(r1=0.154,P<0.05;r2=0.338,P<0.05;r3=0.385,P<0.05);Logistic回归分析结果显示,血清ox-LDL是急性缺血性脑卒中患者颈动脉易损斑块形成的独立危险因素(OR=1.038,95%CI 1.008~1.069,P<0.01)。结论急性缺血性脑卒中患者血清ox-LDL与颈动脉易损斑块的形成独立相关,ox-LDL可以作为临床筛查易损斑块的血清学指标,颈动脉超声联合应用血清学检查可以早期识别可能导致脑缺血事件发生的颈动脉易损斑块。
目的:探討急性缺血性腦卒中患者血清氧化型低密度脂蛋白(ox-LDL)水平與頸動脈易損斑塊的關繫,評估ox-LDL對易損性頸動脈斑塊的識彆能力,為早期識彆易損性頸動脈斑塊探索新的途徑。資料與方法選擇經CT和MRI確診為急性缺血性腦卒中的181例患者,根據頸動脈超聲檢查將其分為無斑塊組48例、穩定斑塊組38例、易損斑塊組95例。檢測血清總膽固醇、三酰甘油、高密度脂蛋白膽固醇、低密度脂蛋白膽固醇、空腹血糖及血清ox-LDL水平,併採用雙功能綵色多普勒超聲檢測頸動脈內膜中層厚度(IMT)、總斑塊麵積(TPA)及斑塊性質,分析血清ox-LDL與缺血性腦卒中危險因素的相關性。結果斑塊組閤併高血壓、血清ox-LDL明顯高于無斑塊組(P<0.05);易損斑塊組血清ox-LDL、TPA明顯高于穩定斑塊組(P<0.01)。血清ox-LDL水平與頸動脈IMT、總膽固醇、LDL-C呈正相關(r1=0.154,P<0.05;r2=0.338,P<0.05;r3=0.385,P<0.05);Logistic迴歸分析結果顯示,血清ox-LDL是急性缺血性腦卒中患者頸動脈易損斑塊形成的獨立危險因素(OR=1.038,95%CI 1.008~1.069,P<0.01)。結論急性缺血性腦卒中患者血清ox-LDL與頸動脈易損斑塊的形成獨立相關,ox-LDL可以作為臨床篩查易損斑塊的血清學指標,頸動脈超聲聯閤應用血清學檢查可以早期識彆可能導緻腦缺血事件髮生的頸動脈易損斑塊。
목적:탐토급성결혈성뇌졸중환자혈청양화형저밀도지단백(ox-LDL)수평여경동맥역손반괴적관계,평고ox-LDL대역손성경동맥반괴적식별능력,위조기식별역손성경동맥반괴탐색신적도경。자료여방법선택경CT화MRI학진위급성결혈성뇌졸중적181례환자,근거경동맥초성검사장기분위무반괴조48례、은정반괴조38례、역손반괴조95례。검측혈청총담고순、삼선감유、고밀도지단백담고순、저밀도지단백담고순、공복혈당급혈청ox-LDL수평,병채용쌍공능채색다보륵초성검측경동맥내막중층후도(IMT)、총반괴면적(TPA)급반괴성질,분석혈청ox-LDL여결혈성뇌졸중위험인소적상관성。결과반괴조합병고혈압、혈청ox-LDL명현고우무반괴조(P<0.05);역손반괴조혈청ox-LDL、TPA명현고우은정반괴조(P<0.01)。혈청ox-LDL수평여경동맥IMT、총담고순、LDL-C정정상관(r1=0.154,P<0.05;r2=0.338,P<0.05;r3=0.385,P<0.05);Logistic회귀분석결과현시,혈청ox-LDL시급성결혈성뇌졸중환자경동맥역손반괴형성적독립위험인소(OR=1.038,95%CI 1.008~1.069,P<0.01)。결론급성결혈성뇌졸중환자혈청ox-LDL여경동맥역손반괴적형성독립상관,ox-LDL가이작위림상사사역손반괴적혈청학지표,경동맥초성연합응용혈청학검사가이조기식별가능도치뇌결혈사건발생적경동맥역손반괴。
PurposeTo investigate the relationship between the serum oxidized low-density lipoprotein (ox-LDL) level and carotid vulnerable plaque in patients with acute cerebral ischemic stroke, and to evaluate the ability of serum ox-LDL in identifying vulnerable carotid plaques.Materials and Methods 181 patients with history of acute cerebral ischemic stroke were recruited. According to the results of carotid ultrasound patients were divided into non plaque group (n=48), stable plaque group (n=38) and vulnerable plaque group (n=95). The serum total cholesterol, triglyceride, high density lipoprotein-cholesterol, low density lipoprotein-cholesterol, fasting plasma glucose and ox-LDL were measured. Carotid intima-medial thickness (CIMT), total carotid plaque area (TPA) and the characters of plaque were examined with color Doppler ultrasound.Results The serum ox-LDL and the number of patients with hypertension in plaque group were significantly higher than that in the non-plaque group (P<0.05). The serum ox-LDL and TPA in the vulnerable plaque group were significantly higher than that in the stable plaque group (P<0.05). Serum ox-LDL in patients with acute cerebral infarction was positively correlated with CIMT, serum total cholesterol and LDL-C (r1=0.154,P<0.05;r2=0.338, P<0.05;r3=0.385,P<0.05). Logistic regression analysis showed that serum ox-LDL was an independent risk factor for carotid vulnerable plaque (OR=1.038, 95%CI 1.008-1.069, P<0.01).Conclusion The serum ox-LDL is independently associated with the formation of vulnerable plaque in patients with acute cerebral infarction. This study suggests that ox-LDL can be used as a biomarker in screening for vulnerable carotid plaque in clinical practice. Carotid ultrasound combined with serology can early identify carotid artery vulnerable plaque that may lead to cerebral ischemic events.