S-100β and Antioxidant Capacity in Cerebrospinal Fluid during and after Thoracic Endovascular Aortic Repair.

International Scholarly Research Notices Pub Date : 2017-06-27 eCollection Date: 2017-01-01 DOI:10.1155/2017/6875195
Koichiro Nandate, Deepak Sharma, Hernando Olivar, Matthew Hallman, Ramesh Ramaiah, Aaron Joffe, Anthony Roche, Vijay Krishnamoorthy
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引用次数: 1

Abstract

Background: Thoracic Endovascular Aortic Repair (TEVAR) has substantially decreased the mortality and major complications from aortic surgery. However, neurological complications such as spinal cord ischemia may still occur after TEVAR. S-100β is a biomarker of central nervous system injury, and oxidant injury plays an important role in neurological injury. In this pilot study, we examined the trends of S-100β and antioxidant capacity in the CSF during and after TEVAR.

Methods: We recruited 10 patients who underwent elective TEVAR. CSF samples were collected through a lumbar catheter at the following time points: before the start of surgery (T0) and immediately (T1) and 24 (T2) and 48 hours (T3) after the deployment of the aortic stent. S-100β and CSF antioxidant capacity were analyzed with the use of commercially available kits.

Results: We observed that the level of S-100β in all of the subjects at 24 hours after the deployment of the aortic stent (T2) increased. However, the levels of S-100β at T1 and T3 were comparable to the baseline value. The antioxidant capacity remained unchanged. No patient had a clinical neurologic complication.

Conclusions: Our observations may indicate biochemical/subclinical central nervous system injury attributable to the deployment of the aortic stent.

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S-100β与胸椎血管内主动脉修复前后脑脊液抗氧化能力的关系
背景:胸主动脉血管内修复术(TEVAR)大大降低了主动脉手术的死亡率和主要并发症。然而,TEVAR术后仍可能出现脊髓缺血等神经系统并发症。S-100β是中枢神经系统损伤的生物标志物,氧化损伤在神经损伤中起重要作用。在这项初步研究中,我们检测了TEVAR期间和之后脑脊液中S-100β和抗氧化能力的变化趋势。方法:我们招募了10例接受选择性TEVAR的患者。在手术开始前(T0)和立即(T1)以及主动脉支架部署后24 (T2)和48小时(T3)通过腰椎导管采集脑脊液样本。使用市售试剂盒分析S-100β和CSF抗氧化能力。结果:我们观察到所有受试者在主动脉支架部署后24小时(T2)的S-100β水平升高。然而,在T1和T3时S-100β水平与基线值相当。抗氧化能力保持不变。无患者出现临床神经系统并发症。结论:我们的观察结果可能表明可归因于主动脉支架部署的生化/亚临床中枢神经系统损伤。
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