Koichiro Nandate, Deepak Sharma, Hernando Olivar, Matthew Hallman, Ramesh Ramaiah, Aaron Joffe, Anthony Roche, Vijay Krishnamoorthy
{"title":"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","authors":"Koichiro Nandate, Deepak Sharma, Hernando Olivar, Matthew Hallman, Ramesh Ramaiah, Aaron Joffe, Anthony Roche, Vijay Krishnamoorthy","doi":"10.1155/2017/6875195","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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-100<i>β</i> 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-100<i>β</i> and antioxidant capacity in the CSF during and after TEVAR.</p><p><strong>Methods: </strong>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 (<i>T</i>0) and immediately (<i>T</i>1) and 24 (<i>T</i>2) and 48 hours (<i>T</i>3) after the deployment of the aortic stent. S-100<i>β</i> and CSF antioxidant capacity were analyzed with the use of commercially available kits.</p><p><strong>Results: </strong>We observed that the level of S-100<i>β</i> in all of the subjects at 24 hours after the deployment of the aortic stent (<i>T</i>2) increased. However, the levels of S-100<i>β</i> at <i>T</i>1 and <i>T</i>3 were comparable to the baseline value. The antioxidant capacity remained unchanged. No patient had a clinical neurologic complication.</p><p><strong>Conclusions: </strong>Our observations may indicate biochemical/subclinical central nervous system injury attributable to the deployment of the aortic stent.</p>","PeriodicalId":14433,"journal":{"name":"International Scholarly Research Notices","volume":"2017 ","pages":"6875195"},"PeriodicalIF":0.0000,"publicationDate":"2017-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504939/pdf/","citationCount":"1","resultStr":"{\"title\":\"S-100<i>β</i> and Antioxidant Capacity in Cerebrospinal Fluid during and after Thoracic Endovascular Aortic Repair.\",\"authors\":\"Koichiro Nandate, Deepak Sharma, Hernando Olivar, Matthew Hallman, Ramesh Ramaiah, Aaron Joffe, Anthony Roche, Vijay Krishnamoorthy\",\"doi\":\"10.1155/2017/6875195\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>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-100<i>β</i> 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-100<i>β</i> and antioxidant capacity in the CSF during and after TEVAR.</p><p><strong>Methods: </strong>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 (<i>T</i>0) and immediately (<i>T</i>1) and 24 (<i>T</i>2) and 48 hours (<i>T</i>3) after the deployment of the aortic stent. S-100<i>β</i> and CSF antioxidant capacity were analyzed with the use of commercially available kits.</p><p><strong>Results: </strong>We observed that the level of S-100<i>β</i> in all of the subjects at 24 hours after the deployment of the aortic stent (<i>T</i>2) increased. However, the levels of S-100<i>β</i> at <i>T</i>1 and <i>T</i>3 were comparable to the baseline value. The antioxidant capacity remained unchanged. No patient had a clinical neurologic complication.</p><p><strong>Conclusions: </strong>Our observations may indicate biochemical/subclinical central nervous system injury attributable to the deployment of the aortic stent.</p>\",\"PeriodicalId\":14433,\"journal\":{\"name\":\"International Scholarly Research Notices\",\"volume\":\"2017 \",\"pages\":\"6875195\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-06-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504939/pdf/\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Scholarly Research Notices\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/2017/6875195\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2017/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Scholarly Research Notices","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2017/6875195","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2017/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
S-100β and Antioxidant Capacity in Cerebrospinal Fluid during and after Thoracic Endovascular Aortic Repair.
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.