• 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

线粒体疾病的功能评估技术

Functional evaluation techniques in mitochondrial disorders.

作者信息

Argov Z

机构信息

Department of Neurology, Hadassah University Hospital, Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Eur Neurol. 1998;39(2):65-71. doi: 10.1159/000007912.

DOI:10.1159/000007912
PMID:9520066
Abstract

Most of the mitochondrial disorders affect the brain and muscle metabolism with variable degrees of impairment. The diagnostic usefulness of the following physiological and imaging methods, which also offer functional information that can be used for follow-up, is critically assessed: lactate levels, exercise testing, phosphorus magnetic resonance spectroscopy (MRS), proton MRS, functional magnetic resonance imaging, positron emission tomography, optical tissue oximetry and single photon emission tomography. Knowledge of the advantages, shortcomings and results of each method in the evaluation of mitochondrial diseases is mandatory before they can be applied to other disorders with suspected oxidative impairment.

摘要

大多数线粒体疾病会影响大脑和肌肉代谢,且损害程度各不相同。以下生理和成像方法的诊断效用,也能提供可用于随访的功能信息,现对此进行严格评估:乳酸水平、运动测试、磷磁共振波谱(MRS)、质子MRS、功能磁共振成像、正电子发射断层扫描、光学组织血氧测定法和单光子发射断层扫描。在将这些方法应用于其他疑似氧化损伤的疾病之前,必须了解每种方法在评估线粒体疾病中的优缺点及结果。

相似文献

1
Functional evaluation techniques in mitochondrial disorders.线粒体疾病的功能评估技术
Eur Neurol. 1998;39(2):65-71. doi: 10.1159/000007912.
2
Brain magnetic resonance in the diagnostic evaluation of mitochondrial encephalopathies.脑磁共振成像在线粒体脑病诊断评估中的应用
Biosci Rep. 2007 Jun;27(1-3):69-85. doi: 10.1007/s10540-007-9046-z.
3
Lactate detection by MRS in mitochondrial encephalopathy: optimization of technical parameters.磁共振波谱法检测线粒体脑病中的乳酸:技术参数的优化
J Neuroimaging. 2008 Jan;18(1):1-8. doi: 10.1111/j.1552-6569.2007.00205.x.
4
Proton MR spectroscopy in the diagnostic evaluation of suspected mitochondrial disease.质子磁共振波谱在疑似线粒体疾病诊断评估中的应用
AJNR Am J Neuroradiol. 2003 Jan;24(1):33-41.
5
Muscle high-energy phosphates in central nervous system disorders. The phosphorus MRS experience.中枢神经系统疾病中的肌肉高能磷酸盐。磷磁共振波谱学经验。
Ital J Neurol Sci. 1997 Dec;18(6):353-7. doi: 10.1007/BF02048238.
6
MR spectroscopy and imaging in metabolic myopathies.代谢性肌病中的磁共振波谱成像
Neurol Clin. 2000 Feb;18(1):35-52. doi: 10.1016/s0733-8619(05)70178-x.
7
Magnetic resonance spectroscopy in migraine: what have we learned so far?偏头痛的磁共振波谱研究:迄今为止我们学到了什么?
Cephalalgia. 2012 Aug;32(11):845-59. doi: 10.1177/0333102412452048. Epub 2012 Jul 4.
8
Altered cerebral glucose metabolism in a family with clinical features resembling mitochondrial neurogastrointestinal encephalomyopathy syndrome in association with multiple mitochondrial DNA deletions.一个具有类似线粒体神经胃肠性脑肌病综合征临床特征并伴有多个线粒体DNA缺失的家族中脑葡萄糖代谢的改变。
Arch Neurol. 2008 Mar;65(3):407-11. doi: 10.1001/archneur.65.3.407.
9
A 31P-magnetic resonance spectroscopy and biochemical study of the mo(vbr) mouse: potential model for the mitochondrial encephalomyopathies.对钼(vbr)小鼠的31P磁共振波谱及生化研究:线粒体脑肌病的潜在模型
Muscle Nerve. 1997 Nov;20(11):1352-9. doi: 10.1002/(sici)1097-4598(199711)20:11<1352::aid-mus2>3.0.co;2-9.
10
Brain MRI and proton MRS findings in infants and children with respiratory chain defects.患有呼吸链缺陷的婴幼儿的脑部磁共振成像和质子磁共振波谱结果
Neuropediatrics. 2005 Oct;36(5):290-301. doi: 10.1055/s-2005-872807.

引用本文的文献

1
Is metabolic flexibility altered in multiple sclerosis patients?多发性硬化症患者的代谢灵活性是否发生改变?
PLoS One. 2012;7(8):e43675. doi: 10.1371/journal.pone.0043675. Epub 2012 Aug 28.
2
Metabolic myopathies: functional evaluation by different exercise testing approaches.代谢性肌病:通过不同运动测试方法进行功能评估
Musculoskelet Surg. 2011 Aug;95(2):59-67. doi: 10.1007/s12306-011-0096-9. Epub 2011 Mar 4.
3
A plasma signature of human mitochondrial disease revealed through metabolic profiling of spent media from cultured muscle cells.
通过培养的肌肉细胞代谢组学分析,揭示了一种人类线粒体疾病的血浆特征。
Proc Natl Acad Sci U S A. 2010 Jan 26;107(4):1571-5. doi: 10.1073/pnas.0906039107. Epub 2010 Jan 8.
4
Proton MR spectroscopy in the diagnostic evaluation of suspected mitochondrial disease.质子磁共振波谱在疑似线粒体疾病诊断评估中的应用
AJNR Am J Neuroradiol. 2003 Jan;24(1):33-41.