• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

生物介质和生物标志物在儿科创伤性脑损伤和神经危重症中的潜力。

The potential for bio-mediators and biomarkers in pediatric traumatic brain injury and neurocritical care.

机构信息

Safar Center for Resuscitation Research, Department of Critical Care Medicine, University of Pittsburgh School of Medicine Pittsburgh, PA, USA.

出版信息

Front Neurol. 2013 Apr 26;4:40. doi: 10.3389/fneur.2013.00040. eCollection 2013.

DOI:10.3389/fneur.2013.00040
PMID:23637695
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3636482/
Abstract

The use of biomarkers of brain injury in pediatric neurocritical care has been explored for at least 15 years. Two general lines of research on biomarkers in pediatric brain injury have been pursued: (1) studies of "bio-mediators" in cerebrospinal fluid (CSF) of children after traumatic brain injury (TBI) to explore the components of the secondary injury cascades in an attempt to identify potential therapeutic targets and (2) studies of the release of structural proteins into the CSF, serum, or urine in order to diagnose, monitor, and/or prognosticate in patients with TBI or other pediatric neurocritical care conditions. Unique age-related differences in brain biology, disease processes, and clinical applications mandate the development and testing of brain injury bio-mediators and biomarkers specifically in pediatric neurocritical care applications. Finally, although much of the early work on biomarkers of brain injury in pediatrics has focused on TBI, new applications are emerging across a wide range of conditions specifically for pediatric neurocritical care including abusive head trauma, cardiopulmonary arrest, septic shock, extracorporeal membrane oxygenation, hydrocephalus, and cardiac surgery. The potential scope of the utility of biomarkers in pediatric neurocritical care is thus also discussed.

摘要

在儿科神经危重症护理中,使用脑损伤生物标志物的研究已经进行了至少 15 年。儿科脑损伤生物标志物的研究主要有两条思路:(1)研究创伤性脑损伤(TBI)后儿童脑脊液(CSF)中的“生物介质”,以探索继发性损伤级联反应的组成部分,试图确定潜在的治疗靶点;(2)研究结构蛋白在脑脊液、血清或尿液中的释放,以诊断、监测和/或预测 TBI 或其他儿科神经危重症患者的病情。大脑生物学、疾病过程和临床应用方面的独特年龄相关差异,要求针对儿科神经危重症应用专门开发和测试脑损伤生物介质和生物标志物。最后,尽管儿科脑损伤生物标志物的早期研究大多集中在 TBI 上,但新的应用正在涌现,涵盖范围广泛的儿科神经危重症疾病,包括虐待性头部创伤、心肺骤停、感染性休克、体外膜氧合、脑积水和心脏手术。因此,本文还讨论了生物标志物在儿科神经危重症护理中的潜在应用范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bc2/3636482/e68d0c2340fa/fneur-04-00040-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bc2/3636482/e68d0c2340fa/fneur-04-00040-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bc2/3636482/e68d0c2340fa/fneur-04-00040-g001.jpg

相似文献

1
The potential for bio-mediators and biomarkers in pediatric traumatic brain injury and neurocritical care.生物介质和生物标志物在儿科创伤性脑损伤和神经危重症中的潜力。
Front Neurol. 2013 Apr 26;4:40. doi: 10.3389/fneur.2013.00040. eCollection 2013.
2
Temporal response profiles of serum ubiquitin C-terminal hydrolase-L1 and the 145-kDa alpha II-spectrin breakdown product after severe traumatic brain injury in children.儿童严重创伤性脑损伤后血清泛素 C 末端水解酶-L1 和 145 kDa αII-血影蛋白降解产物的时间反应曲线
J Neurosurg Pediatr. 2018 Oct;22(4):369-374. doi: 10.3171/2018.4.PEDS17593. Epub 2018 Jun 29.
3
Biofluid biomarkers of traumatic brain injury.创伤性脑损伤的生物流体生物标志物
Brain Inj. 2017;31(9):1195-1203. doi: 10.1080/02699052.2017.1357836.
4
Prognostic value of day-of-injury plasma GFAP and UCH-L1 concentrations for predicting functional recovery after traumatic brain injury in patients from the US TRACK-TBI cohort: an observational cohort study.伤后第 1 天血浆 GFAP 和 UCH-L1 浓度对美国 TRACK-TBI 队列创伤性脑损伤患者功能恢复的预测价值:一项观察性队列研究。
Lancet Neurol. 2022 Sep;21(9):803-813. doi: 10.1016/S1474-4422(22)00256-3.
5
Acute Temporal Profiles of Serum Levels of UCH-L1 and GFAP and Relationships to Neuronal and Astroglial Pathology following Traumatic Brain Injury in Rats.大鼠创伤性脑损伤后血清UCH-L1和GFAP水平的急性时间变化及其与神经元和星形胶质细胞病理学的关系
J Neurotrauma. 2015 Aug 15;32(16):1179-89. doi: 10.1089/neu.2015.3873. Epub 2015 May 14.
6
UCH-L1 is a Poor Serum Biomarker of Murine Traumatic Brain Injury After Polytrauma.UCH-L1 是一种较差的多创伤性脑损伤后小鼠创伤性脑损伤的血清生物标志物。
J Surg Res. 2019 Dec;244:63-68. doi: 10.1016/j.jss.2019.06.023. Epub 2019 Jul 3.
7
Finding effective biomarkers for pediatric traumatic brain injury.寻找小儿创伤性脑损伤的有效生物标志物。
Brain Circ. 2016 Jul-Sep;2(3):129-132. doi: 10.4103/2394-8108.192518. Epub 2016 Oct 18.
8
Translational Metabolomics of Head Injury: Exploring Dysfunctional Cerebral Metabolism with Ex Vivo NMR Spectroscopy-Based Metabolite Quantification头部损伤的转化代谢组学:基于体外核磁共振波谱的代谢物定量分析探索脑代谢功能障碍
9
A Serum Protein Biomarker Panel Improves Outcome Prediction in Human Traumatic Brain Injury.一个血清蛋白质生物标志物组提高了外伤性脑损伤的预后预测。
J Neurotrauma. 2019 Oct 15;36(20):2850-2862. doi: 10.1089/neu.2019.6375. Epub 2019 Jun 19.
10
Predicting Clinical Outcomes 7-10 Years after Severe Traumatic Brain Injury: Exploring the Prognostic Utility of the IMPACT Lab Model and Cerebrospinal Fluid UCH-L1 and MAP-2.预测严重创伤性脑损伤后 7-10 年的临床结局:探索 IMPACT Lab 模型和脑脊液 UCH-L1 和 MAP-2 的预后价值。
Neurocrit Care. 2022 Aug;37(1):172-183. doi: 10.1007/s12028-022-01461-y. Epub 2022 Mar 1.

引用本文的文献

1
Plasma brain-related biomarkers and potential therapeutic targets in pediatric ECMO.小儿体外膜肺氧合中与脑相关的血浆生物标志物及潜在治疗靶点
Neurotherapeutics. 2025 Jan;22(1):e00521. doi: 10.1016/j.neurot.2024.e00521. Epub 2025 Jan 7.
2
Evaluation of neurovascular coupling during neuroprotective therapies: A single site HEAL ancillary study.神经保护治疗期间神经血管耦合的评估:单一地点 HEAL 辅助研究。
Early Hum Dev. 2023 Aug;183:105815. doi: 10.1016/j.earlhumdev.2023.105815. Epub 2023 Jul 3.
3
Abusive Head Trauma Animal Models: Focus on Biomarkers.

本文引用的文献

1
Serum biomarkers of brain injury to classify outcome after pediatric cardiac arrest*.儿童心脏骤停后用于分类结局的脑损伤血清生物标志物*。
Crit Care Med. 2014 Mar;42(3):664-74. doi: 10.1097/01.ccm.0000435668.53188.80.
2
Therapy development for diffuse axonal injury.弥漫性轴索损伤的治疗进展。
J Neurotrauma. 2013 Mar 1;30(5):307-23. doi: 10.1089/neu.2012.2825. Epub 2013 Feb 14.
3
Inflammasome proteins in cerebrospinal fluid of brain-injured patients as biomarkers of functional outcome: clinical article.脑损伤患者脑脊液中的炎症小体蛋白作为功能结局的生物标志物:临床文章。
虐待性头部创伤动物模型:关注生物标志物。
Int J Mol Sci. 2023 Feb 24;24(5):4463. doi: 10.3390/ijms24054463.
4
Pediatric Traumatic Brain Injury: An Update on Preclinical Models, Clinical Biomarkers, and the Implications of Cerebrovascular Dysfunction.小儿创伤性脑损伤:临床前模型、临床生物标志物及脑血管功能障碍影响的最新进展
J Cent Nerv Syst Dis. 2022 May 22;14:11795735221098125. doi: 10.1177/11795735221098125. eCollection 2022.
5
Unravelling neuroinflammation in abusive head trauma with radiotracer imaging.用放射性示踪剂成像技术揭示虐待性头部创伤中的神经炎症。
Pediatr Radiol. 2021 May;51(6):966-970. doi: 10.1007/s00247-021-04995-z. Epub 2021 May 17.
6
Blood Biomarkers for Detection of Brain Injury in COVID-19 Patients.用于检测 COVID-19 患者脑损伤的血液生物标志物。
J Neurotrauma. 2021 Jan 1;38(1):1-43. doi: 10.1089/neu.2020.7332. Epub 2020 Nov 11.
7
Patterns of Osteopontin Expression in Abusive Head Trauma Compared with Other Causes of Pediatric Traumatic Brain Injury.虐待性头部外伤与其他小儿创伤性脑损伤病因的骨桥蛋白表达模式比较。
J Pediatr. 2020 Dec;227:170-175. doi: 10.1016/j.jpeds.2020.06.080. Epub 2020 Jul 2.
8
Neurological Monitoring and Complications of Pediatric Extracorporeal Membrane Oxygenation Support.儿科体外膜肺氧合支持的神经监测和并发症。
Pediatr Neurol. 2020 Jul;108:31-39. doi: 10.1016/j.pediatrneurol.2020.03.014. Epub 2020 Mar 19.
9
Brain metabolism and severe pediatric traumatic brain injury.脑代谢与小儿重型创伤性脑损伤
Childs Nerv Syst. 2017 Oct;33(10):1719-1726. doi: 10.1007/s00381-017-3514-y. Epub 2017 Sep 6.
10
Serum neuron specific enolase is increased in pediatric acute encephalitis syndrome.小儿急性脑炎综合征中血清神经元特异性烯醇化酶升高。
Korean J Pediatr. 2017 Sep;60(9):302-306. doi: 10.3345/kjp.2017.60.9.302. Epub 2017 Sep 21.
J Neurosurg. 2012 Dec;117(6):1119-25. doi: 10.3171/2012.9.JNS12815. Epub 2012 Oct 12.
4
Lipidomics identifies cardiolipin oxidation as a mitochondrial target for redox therapy of brain injury.脂质组学鉴定心磷脂氧化为脑损伤氧化还原治疗的线粒体靶标。
Nat Neurosci. 2012 Oct;15(10):1407-13. doi: 10.1038/nn.3195. Epub 2012 Aug 26.
5
Increased CSF concentrations of myelin basic protein after TBI in infants and children: absence of significant effect of therapeutic hypothermia.婴儿和儿童创伤性脑损伤后脑脊液髓鞘碱性蛋白浓度升高:治疗性低温无显著影响。
Neurocrit Care. 2012 Dec;17(3):401-7. doi: 10.1007/s12028-012-9767-0.
6
Cerebrospinal fluid levels of high-mobility group box 1 and cytochrome C predict outcome after pediatric traumatic brain injury.脑脊髓液中高迁移率族蛋白 B1 和细胞色素 C 水平预测小儿外伤性脑损伤的预后。
J Neurotrauma. 2012 Jul 20;29(11):2013-21. doi: 10.1089/neu.2011.2171. Epub 2012 Apr 27.
7
Biomarkers of brain injury in neonatal encephalopathy treated with hypothermia.新生儿脑病行低温治疗后脑损伤的生物标志物。
J Pediatr. 2012 Sep;161(3):434-40. doi: 10.1016/j.jpeds.2012.02.047. Epub 2012 Apr 10.
8
Guidelines for the acute medical management of severe traumatic brain injury in infants, children, and adolescents--second edition.婴幼儿、儿童及青少年重度创伤性脑损伤急性医疗管理指南——第二版
Pediatr Crit Care Med. 2012 Jan;13 Suppl 1:S1-82. doi: 10.1097/PCC.0b013e31823f435c.
9
Serum concentrations of ubiquitin C-terminal hydrolase-L1 and αII-spectrin breakdown product 145 kDa correlate with outcome after pediatric TBI.血清泛素 C 端水解酶-L1 和 αII-血影蛋白裂解产物 145 kDa 浓度与儿童创伤性脑损伤后的结局相关。
J Neurotrauma. 2012 Jan 1;29(1):162-7. doi: 10.1089/neu.2011.1989.
10
Serum S100B and neuron-specific enolase levels in normothermic and hypothermic infants after perinatal asphyxia.围生期窒息后正常体温和低体温婴儿血清 S100B 和神经元特异性烯醇化酶水平。
Acta Paediatr. 2012 Mar;101(3):319-23. doi: 10.1111/j.1651-2227.2011.02480.x. Epub 2011 Nov 2.