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髓鞘碱性蛋白、S100钙结合蛋白B与脑梗死介入治疗后早期神经功能恶化风险的关联性研究

Association of Myelin Basic Protein and S100 Calcium-Binding Protein B With the Risk of Early Neurological Deterioration After Interventional Therapy for Cerebral Infarction

  • 摘要:
    目的 探析脑梗死患者髓鞘碱性蛋白(myelin basic protein, MBP)、S100钙结合蛋白B(S100 calcium-binding protein B, S100-B)水平与介入治疗后早期神经功能恶化的关联性。
    方法 纳入2021年7月–2024年7月期间本院收治的258例脑梗死患者,采用美国国立卫生研究院卒中量表(National Institutes of Health Stroke Scale, NIHSS)评分评估患者的神经功能状况,将死亡患者或介入治疗24 h后NIHSS评分增加4分及以上患者纳入早期神经功能恶化组,其余患者纳入未恶化组。测定所有患者MBP、S100-B水平,并分析其水平变化与介入治疗后神经功能恶化风险的关系。
    结果 脑梗死患者早期神经功能恶化组血清MBP、S100-B水平高于未恶化组〔t=9.062(95%CI:2.348~3.663)、7.708(95%CI:0.221~0.375),P<0.001〕;Spearman相关性显示:恶化组血清MBP、S100-B水平与NIHSS评分增加情况呈正相关〔r=0.323(95%CI:0.095~0.542)、0.292(95%CI:0.066~0.488),P<0.05〕;分层回归分析显示:血清MBP〔比值比(odds ratio, OR)=1.996,95%CI:1.607~2.478〕、S100-B(OR=1.005,95%CI:1.003~1.007)水平是影响脑梗死患者早期神经功能恶化的危险因素(P<0.05),即使校正混杂因素后依然是其危险因素,此外入院NIHSS评分(OR=1.224,95%CI:1.142~1.310)及合并高血压(OR=2.542,95%CI:1.139~5.669)、高脂血症(OR=2.618,95%CI:1.101~6.228),其中入院NIHSS评分与MBP存在交互作用(OR=1.081,95%CI:1.034~1.130);受试者工作特征曲线显示:血清MBP、S100-B水平评估脑梗死患者早期神经功能恶化的曲线下面积分别为0.822(95%CI:0.764~0.879)、0.788(95%CI:0.724~0.853)。
    结论 脑梗死患者介入治疗后血清MBP、S100-B水平较高与早期神经功能恶化风险相关,且对神经功能恶化风险有一定的评估价值。

     

    Abstract:
    Objective To investigate and analyze the association of serum levels of myelin basic protein (MBP) and S100 calcium-binding protein B (S100-B) with early neurological deterioration in patients with cerebral infarction after interventional therapy.
    Methods A total of 258 patients with cerebral infarction, admitted to our hospital between July 2021 and July 2024, were enrolled. The National Institutes of Health Stroke Scale (NIHSS) was used to evaluate the neurological function status of patients. Patients who died or whose NIHSS score increased by 4 points or more after 24 hours of interventional therapy were included in the early neurological deterioration group, while the remaining patients were included in the non-deterioration group. The levels of MBP and S100-B in all patients were measured, and the relationship between changes in MBP and S100-B levels and the risk of neurological deterioration after interventional therapy was analyzed.
    Results The levels of serum MBP and S100-B of patients with cerebral infarction were markedly higher in the early neurological deterioration group compared with those in the non-deterioration group (t = 9.062 95% CI: 2.348-3.663 and 7.708 95% CI: 0.221-0.375, P < 0.001). Spearman correlation analysis showed that the levels of serum MBP and S100-B in the deterioration group were positively correlated with NIHSS score increase (r = 0.323 95% CI: 0.095-0.542 and 0.292 95% CI: 0.066-0.488, P < 0.05). Stratified regression analysis showed that serum MBP (OR = 1.996, 95% CI: 1.607-2.478) and S100-B (OR = 1.005, 95% CI: 1.003-1.007) were risk factors affecting the early deterioration of neurological function in patients with cerebral infarction (P < 0.05), even after adjusting for confounding factors. In addition, admission NIHSS score (OR = 1.224, 95% CI: 1.142-1.310), hypertension (OR = 2.542, 95% CI: 1.139-5.669) and hyperlipidemia (OR = 2.618, 95% CI: 1.101-6.228) were also risk factors, and an interaction effect between the admission NIHSS score and MBP (OR = 1.081, 95% CI: 1.034-1.130) was observed. Receiver operating characteristic (ROC) curve analysis showed that the area under the curve (AUC) of serum MBP and S100-B in evaluating early neurological deterioration were 0.822 (95% CI: 0.764-0.879) and 0.788 (95% CI: 0.724-0.853), respectively.
    Conclusion Elevated levels of serum MBP and S100-B in patients with cerebral infarction after interventional therapy are associated with an increased risk of early neurological deterioration and show potential value for assessing the risk of neurological deterioration.

     

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