Tjili Tondi Maspian, July Julius, Darwin Eryati, Syafrita Yuliarni, Suntoro Vanessa Angelica, Lukito Patrick Putra, Setiawan Jonathan
Department of Neurosurgery, Arifin Achmad National Hospital, Pekanbaru, Indonesia.
Department of Neurosurgery, Neuroscience Center Siloam Hospital, Tangerang, Indonesia.
Surg Neurol Int. 2025 Jun 27;16:268. doi: 10.25259/SNI_20_2025. eCollection 2025.
Endothelial dysfunction plays a key role in intracerebral hemorrhage (ICH), with vascular endothelial cadherin (VE-cadherin) being essential for maintaining blood vessel integrity and the blood-brain barrier. Hypertension increases ICH risk by damaging blood vessel integrity due to inflammatory cascades. Lower VE-cadherin levels in hypertensive patients suggest its potential as an early predictor of ICH risk.
This 12-month study included 40 hypertensive control patients and 40 hypertensive patients with nonlobar ICH. Blood samples were analyzed using enzyme-linked immunosorbent assays to measure VEcadherin, interferon gamma, and interleukin-17 levels. Receiver operating characteristic analysis determined a VE-cadherin cutoff value, and a regression model assessed its association with ICH risk.
A VE-cadherin cutoff value of 400.8 pg/dL was identified, with higher levels independently linked to lower odds of nonlobar ICH. VE-cadherin was the only biomarker that remained statistically significant in the regression model. These findings suggest that reduced VE-cadherin levels contribute to ICH development, and its measurement may help identify high-risk patients for early intervention.
VE-cadherin dysfunction in hypertension may serve as a predictor of nonlobar ICH risk. Its protective role highlights its potential as a biomarker for risk assessment and prevention strategies in hypertensive patients. These findings may pave the way for targeted interventions in hypertensive populations, warranting further research to confirm its clinical utility.
内皮功能障碍在脑出血(ICH)中起关键作用,血管内皮钙黏蛋白(VE-钙黏蛋白)对于维持血管完整性和血脑屏障至关重要。高血压通过炎症级联反应破坏血管完整性,从而增加脑出血风险。高血压患者中较低的VE-钙黏蛋白水平表明其有可能作为脑出血风险的早期预测指标。
这项为期12个月的研究纳入了40名高血压对照患者和40名非叶性脑出血的高血压患者。使用酶联免疫吸附测定法分析血样,以测量VE-钙黏蛋白、干扰素γ和白细胞介素-17水平。通过受试者工作特征分析确定VE-钙黏蛋白的临界值,并通过回归模型评估其与脑出血风险的关联。
确定VE-钙黏蛋白的临界值为400.8 pg/dL,较高水平与非叶性脑出血的较低几率独立相关。VE-钙黏蛋白是回归模型中唯一在统计学上具有显著意义的生物标志物。这些发现表明,VE-钙黏蛋白水平降低会促使脑出血的发生,测量其水平可能有助于识别高危患者以便进行早期干预。
高血压中的VE-钙黏蛋白功能障碍可能作为非叶性脑出血风险的预测指标。其保护作用凸显了它作为高血压患者风险评估和预防策略生物标志物的潜力。这些发现可能为高血压人群的靶向干预铺平道路,有待进一步研究以证实其临床效用。