首页|急性脑梗死患者血清趋化因子CXCL12、RANTES、MIP-1α的动态表达及与神经功能缺损程度和预后的相关性分析

急性脑梗死患者血清趋化因子CXCL12、RANTES、MIP-1α的动态表达及与神经功能缺损程度和预后的相关性分析

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目的:探究急性脑梗死(ACI)患者CXC基序趋化因子配体 12(CXCL12)、调节激活正常T细胞表达和分泌细胞因子(RANTES)、巨噬细胞炎性蛋白-1α(MIP-1α)的动态表达及与神经功能缺损程度和预后的相关性.方法:选取 2021 年 7 月—2022 年 7 月赣州市第三人民医院收治的 80 例ACI患者作为ACI组,另选取同期脑神经功能正常的 80 例志愿者作为对照组.比较ACI组与对照组、不同神经功能缺损程度及预后情况患者的CXCL12、RANTES、MIP-1α水平;分析上述血清指标与神经功能缺损程度的相关性;绘制受试者操作特征(ROC)曲线分析各血清指标对ACI患者预后不良的预测价值.结果:ACI组CXCL12、RANTES、MIP-1α水平均高于对照组(P<0.05).重度缺损组血清CXCL12、RANTES、MIP-1α水平高于轻、中度缺损组,且中度缺损组均高于轻度缺损组(P<0.05).预后不良组血清CXCL12、RANTES、MIP-1α水平均高于预后良好组(P<0.05).Kendall的tau-b相关性分析显示,ACI患者血清CXCL12、RANTES、MIP-1α水平与神经功能缺损程度均呈正相关(τ=0.566、0.678、0.752,P<0.001).ROC曲线显示,血清CXCL12、RANTES、MIP-1α水平单一及联合检测预测ACI患者预后不良的曲线下面积(AUC)均>0.8,联合检测的价值更高.结论:ACI患者血清CXCL12、RANTES、MIP-1α水平均呈高表达,且水平越高,患者的神经功能缺损越严重、预后不良风险越高.
Analysis of Dynamic Expression of Serum Chemokine CXCL12,RANTES,MIP-1α and Its Correlation with the Degree of Neurological Function Defect and Prognosis in Patients with Acute Cerebral Infarction
Objective:To investigate the dynamic expression of serum chemokine CXC motif chemokine ligand 12(CXCL12),regulated upon activation normal T cell expressed and secreted(RANTES),macrophage inflammatory protein-1α(MIP-1α)and its correlation with the degree of neurological function defect and prognosis in patients with acute cerebral infarction.Method:A total of 80 ACI patients admitted to the Third People's Hospital of Ganzhou from July 2021 to July 2022 were selected as ACI group,and another 80 volunteers with normal neurological function during the same period were selected as control group.The levels of CXCL12,RANTES and MIP-1α were compared between ACI group and control group,different degree of neurological function defect and prognosis situation.The correlation between the above serum indexes and the degree of neurological function defect were analyzed.Receiver operator characteristic(ROC)curve was drawn to analyze the predictive value of various serum indexes for poor prognosis of ACI patients.Result:The levels of CXCL12,RANTES and MIP-1α in ACI group were higher than those in control group(P<0.05).The levels of CXCL12,RANTES and MIP-1α in severe defect group were higher than those in mild and moderate defect group,and those in moderate defect group were higher than those in mild defect group(P<0.05).The levels of CXCL12,RANTES and MIP-1α in poor prognosis group were higher than those in good prognosis group(P<0.05).Kendall's tau-b correlation analysis showed that the levels of serum CXCL12,RANTES and MIP-1α were positively correlated with the degree of neurological function defect in ACI patients(τ=0.566,0.678,0.752,P<0.001).ROC curve showed that the area under the curve(AUC)of serum CXCL12,RANTES and MIP-1α levels single and combined detection were all greater than 0.8 in predicting the poor prognosis of ACI patients,and the combined detection had a higher value.Conclusion:Serum CXCL12,RANTES and MIP-1α levels in ACI patients are all highly expressed,and the higher the level,the more serious the neurological function defect and the higher the risk of poor prognosis.

Acute cerebral infarctionCXC motif chemokine ligand 12Regulated upon activation normal T cell expressed and secretedMacrophage inflammatory protein-1αNeurological function defectPrognosis

温辉、曹骏、陈吉祥、张广彪

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赣州市第三人民医院急诊科 江西 赣州 341000

赣州市第三人民医院老年内科 江西 赣州 341000

赣州市第三人民医院伴躯体疾病精神科 江西 赣州 341000

急性脑梗死 CXC基序趋化因子配体12 调节激活正常T细胞表达和分泌细胞因子 巨噬细胞炎性蛋白-1α 神经功能缺损 预后

江西省卫生健康委科技计划项目

202312060

2024

中国医学创新
中国保健协会

中国医学创新

影响因子:1.706
ISSN:1674-4985
年,卷(期):2024.21(4)
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