Guidelines for using proton MR spectroscopy in multicenter clinical MS studies

被引:86
作者
De Stefano, N.
Filippi, M.
Miller, D.
Pouwels, P. J.
Rovira, A.
Gass, A.
Enzinger, C.
Matthews, P. M.
Arnold, D. L.
机构
[1] Univ Siena, Dept Neurol & Behav Sci, Neurol & Neurometab Unit, I-53100 Siena, Italy
[2] Univ Milan, Osped San Raffaele, Sci Inst & Univ, Dept Neurol,Neuroimaging Res Unit, I-20127 Milan, Italy
[3] UCL, Inst Neurol, Dept Neuroinflammat, NMR Res Unit, London WC1E 6BT, England
[4] Vrije Univ Amsterdam Med Ctr, Dept Radiol, Amsterdam, Netherlands
[5] Hosp Valle De Hebron, Magnet Resonance Unit, Dept Radiol, Barcelona, Spain
[6] Kantonsspital, Univ Hosp, Dept Neurol, CH-4031 Basel, Switzerland
[7] Med Univ Graz, Dept Neurol, Graz, Austria
[8] Univ London Imperial Coll Sci Technol & Med, Dept Clin Neurol, London, England
[9] Montreal Neurol Inst, McConnell Brain Imaging Ctr, Quebec City, PQ, Canada
关键词
D O I
10.1212/01.wnl.0000291557.62706.d3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Proton MR spectroscopy (MRS) allows noninvasive characterization of chemical-pathologic changes in the brain. In patients with multiple sclerosis (MS), proton MRS reveals chemical pathology in focal inflammatory lesions as well as in regions of the brain that are not associated with structural abnormalities on conventional MRI. In MS studies, it has been particularly useful as a method for the assessment of neurodegeneration based on decreases in the levels of the neuroaxonal marker compound, N-acetylaspartate. Also, MRS has provided evidence of chemical pathology and repair involving non-neuronal brain cells based on changes in metabolites, including choline, myo-inositol, glutamate, and GABA. Despite its greater pathologic specificity for axonal integrity compared to conventional MRI, MRS has been used only infrequently in clinical trials. This prompted us to review current MRS clinical applications in MS, discuss the potential and limitations of the technique, and suggest recommendations for the application of MRS to clinical trials.
引用
收藏
页码:1942 / 1952
页数:11
相关论文
共 94 条
[11]  
Bitsch A, 1999, AM J NEURORADIOL, V20, P1619
[12]   N-acetylaspartate is an axon-specific marker of mature white matter in vivo: A biochemical and immunohistochemical study on the rat optic nerve [J].
Bjartmar, C ;
Battistuta, J ;
Terada, N ;
Dupree, E ;
Trapp, BD .
ANNALS OF NEUROLOGY, 2002, 51 (01) :51-58
[13]   THE PROTON NMR-SPECTRUM IN ACUTE EAE - THE SIGNIFICANCE OF THE CHANGE IN THE CHO-CR RATIO [J].
BRENNER, RE ;
MUNRO, PMG ;
WILLIAMS, SCR ;
BELL, JD ;
BARKER, GJ ;
HAWKINS, CP ;
LANDON, DN ;
MCDONALD, WI .
MAGNETIC RESONANCE IN MEDICINE, 1993, 29 (06) :737-745
[14]   Lesion heterogeneity in multiple sclerosis: a study of the relations between appearances on T1 weighted images, T1 relaxation times, and metabolite concentrations [J].
Brex, PA ;
Parker, GJM ;
Leary, SM ;
Molyneux, PD ;
Barker, GJ ;
Davie, CA ;
Thompson, AJ ;
Miller, DH .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2000, 68 (05) :627-632
[15]   MULTIPLE-SCLEROSIS IN CHILDREN - CEREBRAL METABOLIC ALTERATIONS MONITORED BY LOCALIZED PROTON MAGNETIC-RESONANCE SPECTROSCOPY INVIVO [J].
BRUHN, H ;
FRAHM, J ;
MERBOLDT, KD ;
HANICKE, W ;
HANEFELD, F ;
CHRISTEN, HJ ;
KRUSE, B ;
BAUER, HJ .
ANNALS OF NEUROLOGY, 1992, 32 (02) :140-150
[16]   1H-MRS quantification of tNA and tCr in patients with multiple sclerosis:: a meta-analytic review [J].
Caramanos, Z ;
Narayanan, S ;
Arnold, DL .
BRAIN, 2005, 128 :2483-2506
[17]   Brain metabolite changes in cortical grey and normal-appearing white matter in clinically early relapsing-remitting multiple sclerosis [J].
Chard, DT ;
Griffin, CM ;
McLean, MA ;
Kapeller, P ;
Kapoor, R ;
Thompson, AJ ;
Miller, DH .
BRAIN, 2002, 125 :2342-2352
[18]   Thalamic neurodegeneration in multiple sclerosis [J].
Cifelli, A ;
Arridge, M ;
Jezzard, P ;
Esiri, MM ;
Palace, J ;
Matthews, PM .
ANNALS OF NEUROLOGY, 2002, 52 (05) :650-653
[19]  
COYLE JT, 1989, ALLOSTERIC MODULATIO, P319
[20]  
Danielsen E.R., 1999, MAGNETIC RESONANCE S