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血清神经元特异性烯醇化酶、血管生成素-1、血管生成素样蛋白-3与脑梗死患者病情严重程度的相关性及对预后评估价值

Correlation of Serum Neuron-Specific Enolase, Angiopoietin-1, and Angiopoietin-Like Protein-3 With Disease Severity and Their Prognostic Value in Patients With Cerebral Infarction

  • 摘要:
    目的 探讨血清神经元特异性烯醇化酶(neuron-specific enolase, NSE)、血管生成素-1(angiopoietin-1, Ang-1)、血管生成素样蛋白-3(angiopoietin-like protein-3, ANGPTL3)与脑梗死患者病情严重程度及预后的相关性。
    方法 选取江西省九江市第一人民医院神经内科2022年2月–2024年5月收治的510例脑梗死患者,根据病情严重程度将其分为轻症组(n=192)、中症组(n=215)、重症组(n=103),经治疗后再分为预后良好组(n=384)、预后不良组(n=126),同期选121例健康人群作为对照组(n=121)。检测所有患者入院时血清NSE、Ang-1、ANGPTL3水平,分析三者与脑梗死患者病情严重程度的相关性,并采用ROC曲线分析三者及联合对脑梗死患者预后不良的预测价值。
    结果 重症组患者血清NSE、ANGPTL3高于中症组与轻症组,而血清Ang-1则低于中症组与轻症组(P均<0.05);Spearman相关性显示,血清NSE、ANGPTL3与脑梗死患者病情严重程度呈正相关关系(r=0.179、0.313;P<0.05),血清Ang-1与其呈负相关关系(r=-0.187;P<0.05);观察预后发现,预后不良组患者血清NSE、ANGPTL3高于预后良好组,血清Ang-1低于预后良好组(P均<0.05);经logistic多因素回归分析得出,血清NSE(OR=1.228,95%CI:1.146~1.316)、Ang-1(OR=0.059,95%CI:0.020~0.178)、ANGPTL3(OR=1.334,95%CI:1.256~1.417)均是影响脑梗死患者预后的主要因素(P均<0.05);利用ROC曲线评估发现,血清NSE、Ang-1、ANGPTL3三者联合的AUC为0.904(0.871~0.936),敏感度、特异度为79.40%、89.60%。Hosmer-Lemeshow结果:χ2=7.423,P=0.492,模型预测效能较高。
    结论 血清NSE、ANGPTL3水平高及Ang-1水平低与脑梗死病情严重程度及预后紧密相关,临床关注三者水平变化对患者的治疗有一定指导意义。

     

    Abstract:
    Objective To investigate the association between the disease severity and prognosis of cerebral infarction patients and serum levels of neuron-specific enolase (NSE), angiopoietin-1 (Ang-1), and angiopoietin-like protein-3 (ANGPTL3).
    Methods A total of 510 patients with cerebral infarction admitted to the Department of Neurology, the First People's Hospital of Jiujiang City, Jiangxi Province between February 2022 and May 2024 were enrolled. According to their disease severity, the patients were divided into a mild group (n = 192), a moderate group (n = 215), and a severe group (n = 103). After treatment, the patients were further divided into a good prognosis group (n = 384) and a poor prognosis group (n = 126). During the same period, 121 healthy individuals were included as a control group. During the same period, 121 healthy individuals were included in a control group. Serum levels of NSE, Ang-1, and ANGPTL3 of all patients were measured upon admission. The correlations between these biomarkers and disease severity were analyzed. The predictive value of each biomarker alone and that of the 3 biomarkers in combination for poor prognosis in patients with cerebral infarction were assessed using receiver operating characteristic (ROC) curves.
    Results Serum NSE and ANGPTL3 levels in the severe group were significantly higher than those in the moderate and mild groups, whereas the serum Ang-1 levels in the severe group were significantly lower than those in the moderate and mild groups (all P < 0.05). Spearman correlation analysis showed that serum NSE and ANGPTL3 levels were positively correlated with disease severity (r = 0.179 and 0.313, respectively, P < 0.05), while serum Ang-1 levels were negatively correlated with disease severity (r = -0.187, P < 0.05). Prognostic analysis revealed that serum NSE and ANGPTL3 levels were higher, while serum Ang-1 levels were lower, in the poor prognosis group compared with the good prognosis group (all P < 0.05). Multivariate logistic regression revealed that serum levels of NSE (odds ratio OR = 1.228, 95% CI: 1.146-1.316), Ang-1 (OR = 0.059, 95% CI: 0.020-0.178), and ANGPTL3 (OR = 1.334, 95% CI: 1.256-1.417) were major factors associated with prognosis in patients with cerebral infarction (all P < 0.05). ROC curves showed that serum NSE, Ang-1, and ANGPTL3 levels in combination yielded an area under the curve (AUC) of 0.904 (95% CI: 0.871-0.936), with a sensitivity of 79.40% and a specificity of 89.60%. The Hosmer–Lemeshow test of the model showed a good predictive performance (χ2 = 7.423, P = 0.492).
    Conclusion The severity and prognosis of cerebral infarction patients are strongly correlated with high serum NSE and ANGPTL3 levels and low Ang-1 levels. Monitoring changes in these 3 biomarkers may inform clinical treatment of patients with cerebral infarction.

     

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