大动脉粥样硬化型脑卒中早期神经功能恶化的预测模型构建OA
Predictive modeling of early neurological deterioration in large artery atherosclerotic stroke
目的:探讨急性缺血性脑卒中 TOAST分型为大动脉粥样硬化型(large artery atherosclerosis,LAA)患者发生早期神经功能恶化(early neurological deterioration,END)的危险因素,建立列线图预测模型并对其进行评价.方法:连续纳入2023年10月~2024年9月期间在我院住院治疗的大动脉粥样硬化型急性缺血性脑卒中(LAA-AIS)患者.根据发病后7 d内NIHSS评分总分增加≥2分或运动功能的评分增加≥1分将患者分为END组和非END组.应用SPSS27.0行单因素分析,对于P<0.05的变量使用二元Logistic回归分析,筛选出LAA-AIS患者发生END的独立危险因素,构建列线图预测模型.采用ROC曲线及其曲线下面积(AUC)值评估模型的区分度,采用校准曲线评估模型准确度,采用决策曲线分析(decision curve analysis,DCA)评估模型的临床实用性.结果:共纳入249例LAA-AIS患者,其中男性190例(76.3%),女性59例(23.7%),年龄63(53,73)岁;END组62例(24.9%),非END组187例(75.1%).单因素分析发现6个变量具有统计学差异(P<0.05),将其纳入二元 Logistic 回归分析后筛选出 4 个变量:BMI(OR=1.171,95%CI 1.032~1.329,P=0.015)、入院时收缩压(OR=1.015,95%CI 1.001~1.030,P=0.030)、糖化血红蛋白(OR=1.286,95%CI 1.064~1.555,P=0.009)、低密度脂蛋白胆固醇(LDL-C)(OR=2.278,95%CI 1.272~4.079,P=0.006)是LAA-AIS患者发生END的独立危险因素.基于上述4个因素构建列线图预测模型,采用 Bootstrap法进行内部验证,绘制 ROC曲线、校准曲线、DCA曲线.结果显示该模型的 AUC为0.735;校准图预测值与实际值一致性较好,DCA曲线显示预测模型具有较高临床实用性.结论:低密度脂蛋白胆固醇、入院时收缩压、BMI及糖化血红蛋白水平升高是LAA-AIS患者发生END的独立危险因素,据此建立的列线图预测模型是一种可靠且易于使用的预测LAA-AIS患者发生END的工具.
Objective:To investigate the risk factors for early neurological deterioration(END)in patients with acute ischemic stroke with TOAST classification of large artery atherosclerosis(LAA),and to establish a nomogram prediction model and evalu-ate it.Methods:Consecutive patients with large-artery atherosclerotic acute ischemic stroke(LAA-AIS)who were hospitalized in our hospital between October 2023 and September 2024 were included.Patients were categorized into END and non-END groups based on an increase of≥2 points in the total NIHSS score or an increase of≥1 point in the score of motor function within 7 d af-ter onset.SPSS27.0 was applied to perform univariate analysis,and binary Logistic regression analysis was used for variables with P<0.05 to screen out the independent risk factors for END in LAA-AIS patients,a nomogram prediction model was constructed.The ROC curve and its area under the curve(AUC)value were used to assess the differentiation of the model,the calibration curve was used to assess the accuracy of the model,and the decision curve analysis(DCA)was used to assess the clinical utility of the model.Results:A total of 249 patients with LAA-AIS were included,including 190(76.3%)males and 59(23.7%)fe-males,aged 63(53,73)years;62(24.9%)in the END group and 187(75.1%)in the non-END group.Univariate analysis found 6 variables to be statistically different(P<0.05),and 4 variables were screened out by including them in binary Logistic re-gression analysis:BMI(OR=1.171,95%CI 1.032 to 1.329,P=0.015),systolic blood pressure at admission(OR=1.015,95%CI 1.001 to 1.030,P=0.030),glycosylated hemoglobin(OR=1.286,95%CI 1.064 to 1.555,P=0.009),and low-density lipoprotein cholesterol(LDL-C)(OR=2.278,95%CI 1.272 to 4.079,P=0.006)were the independent risk factors for the devel-opment of END in LAA-AIS patients.A nomogram prediction model was constructed based on the above 4 factors,and internal validation was performed using the Bootstrap method to draw ROC curves,calibration curves,and DCA curves.The results showed that the AUC of the model was 0.735;the calibration plot predicted values were in good agreement with the actual values,and the DCA curve showed that the prediction model had high clinical utility.Conclusion:Elevated LDL cholesterol,systolic blood pressure on admission,BMI,and glycosylated hemoglobin levels are independent risk factors for the development of END in patients with LAA-AIS,and the column-line graphic prediction model based on them is a reliable and easy-to-use tool for pre-dicting the development of END in patients with LAA-AIS.
李响花;黄培君;郑冰冰;崔凯丽;杨慧;陈斌;游咏
海南医科大学第二附属医院神经内科,海南 海口,570311海南医科大学第二附属医院神经内科,海南 海口,570311海南医科大学公共卫生学院,海南 海口,571199海南医科大学第二附属医院神经内科,海南 海口,570311海南医科大学第二附属医院神经内科,海南 海口,570311海南医科大学第二附属医院神经内科,海南 海口,570311海南医科大学第二附属医院神经内科,海南 海口,570311
医药卫生
大动脉粥样硬化脑卒中早期神经功能恶化危险因素列线图
Large artery atherosclerosisStrokeEarly neurologic deteriorationRisk factorsNomogram
《海南医科大学学报》 2026 (12)
900-907,8
This study was supported by the National Natural Science Foundation of China(82360230)Key Research and Development Projects of Hainan Provincial Science and Technology Department(ZDYF2022SHFZ108) 国家自然科学基金(82360230)海南省科技厅重点研发项目(ZDYF2022SHFZ108)
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