Plasma Extracellular Matrix Protein 2 Level as a Predictive Biomarker for Rupture of Small Intracranial Aneurysms

IF 2.8 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Chenchen Wang, Yuwei Han, Da Huo, Xiaoming Li, Guobiao Liang
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Abstract

As the neuroimaging technology improves, the detection rate of unruptured intracranial aneurysms (UIA) is gradually increasing. However, there is currently no effective means to evaluate and predict the risk of rupture for small intracranial aneurysm (sIA, diameter < 7 mm). We previously identified extracellular matrix protein 2 (ECM2) as a potential candidate biomarker for predicting intracranial aneurysm (IA) rupture through iTRAQ combined with LC–MS/MS protein quantification technology, so this study aimed to further validate the ability of plasma ECM2 expression levels to predict IA rupture. This prospective, observational, single-center cohort study enrolled 322 individuals with ruptured intracranial aneurysm (RIA, N = 123), UIA (N = 89), traumatic subarachnoid hemorrhage (tSAH, N = 55), or healthy controls (HC, N = 55). ECM2 plasma levels were quantified using enzyme-linked immunosorbent assay (ELISA). The Spearman rank correlation analysis was employed to examine the relationship between variables. Independent risk factors of sIA rupture were identified using logistic regression analysis. The ROC curve assessed the predictive capability for sIA rupture. Plasma ECM2 was notably higher in RIA patients than in UIA, tSAH, and HC groups. Plasma ECM2 levels showed no significant difference among the asymptomatic UIA, HC, and tSAH groups. There was also no significant difference in plasma ECM2 levels between symptomatic UIA patients and RIA patients. Furthermore, the plasma ECM2 level was closely related to hypertension history in sIA patients. ECM2 plasma level was an independent risk factor for sIA rupture. The plasma ECM2 cutoff level for predicting IA rupture was determined to be 1540.67 pg/ml. The combination of ECM2 levels and aneurysm location increased predictive accuracy (AUC = 0.828, sensitivity 87.0%, specificity 68.8%, accuracy 83.2%), surpassing the performance of PHASES and ELPASS scores. ECM2 could potentially act as an early warning biomarker for predicting the rupture of sIAs.

Abstract Image

血浆细胞外基质蛋白2水平作为预测颅内小动脉瘤破裂的生物标志物
随着神经影像学技术的进步,颅内未破裂动脉瘤(UIA)的检出率逐渐提高。然而,目前还没有有效的方法来评估和预测颅内小动脉瘤(sIA,直径<; 7mm)破裂的风险。我们之前通过iTRAQ结合LC-MS /MS蛋白定量技术确定了细胞外基质蛋白2 (ECM2)作为预测颅内动脉瘤(IA)破裂的潜在候选生物标志物,因此本研究旨在进一步验证血浆ECM2表达水平预测IA破裂的能力。这项前瞻性、观察性、单中心队列研究纳入了322例颅内动脉瘤破裂(RIA, N = 123)、UIA (N = 89)、外伤性蛛网膜下腔出血(tSAH, N = 55)或健康对照(HC, N = 55)患者。采用酶联免疫吸附法(ELISA)定量测定血浆ECM2水平。采用Spearman秩相关分析检验变量间的关系。采用logistic回归分析确定sIA破裂的独立危险因素。ROC曲线评估sIA破裂的预测能力。RIA患者血浆ECM2明显高于UIA、tSAH和HC组。血浆ECM2水平在无症状UIA、HC和tSAH组之间无显著差异。有症状的UIA患者和RIA患者血浆ECM2水平也无显著差异。此外,sIA患者血浆ECM2水平与高血压病史密切相关。血浆ECM2水平是sIA破裂的独立危险因素。预测IA破裂的血浆ECM2临界值为1540.67 pg/ml。ECM2水平与动脉瘤位置的结合提高了预测准确性(AUC = 0.828,敏感性87.0%,特异性68.8%,准确性83.2%),超过了分期和ELPASS评分的表现。ECM2可能作为预测sIAs破裂的早期预警生物标志物。
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来源期刊
Journal of Molecular Neuroscience
Journal of Molecular Neuroscience 医学-神经科学
CiteScore
6.60
自引率
3.20%
发文量
142
审稿时长
1 months
期刊介绍: The Journal of Molecular Neuroscience is committed to the rapid publication of original findings that increase our understanding of the molecular structure, function, and development of the nervous system. The criteria for acceptance of manuscripts will be scientific excellence, originality, and relevance to the field of molecular neuroscience. Manuscripts with clinical relevance are especially encouraged since the journal seeks to provide a means for accelerating the progression of basic research findings toward clinical utilization. All experiments described in the Journal of Molecular Neuroscience that involve the use of animal or human subjects must have been approved by the appropriate institutional review committee and conform to accepted ethical standards.
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