Changes in putamen N-acetylaspartate and choline ratios in untreated and levodopa-treated Parkinson's disease: A proton magnetic resonance spectroscopy study

被引:67
作者
Ellis, CM
Lemmens, G
Williams, SCR
Simmons, A
Dawson, J
Leigh, PN
Chaudhuri, KR
机构
[1] UNIV LONDON KINGS COLL HOSP, MOVEMENT DISORDERS & NEURODEGENERAT UNIT, LONDON, ENGLAND
[2] UNIV LONDON KINGS COLL HOSP, INST PSYCHIAT, DEPT CLIN NEUROSCI, LONDON, ENGLAND
[3] MAUDSLEY HOSP & INST PSYCHIAT, DEPT NEUROIMAGING, LONDON SE5 8AZ, ENGLAND
关键词
D O I
10.1212/WNL.49.2.438
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We have carried out single-voxel proton magnetic resonance spectroscopy centered on the putamen both ipsilateral and contralateral to the worst affected side in nine subjects with drug naive idiopathic Parkinson's disease (IPD); seven chronically levodopa-treated dyskinetic IPD subjects; and 11 age-matched healthy controls. Measurements of N-acetylaspartate (NAA)/choline (Cho), NAA/(Creatine + Phosphocreatine) (Cr+PCr), and Cho/(Cr+PCr) were made. We found a significant reduction in NAA/Cho ratios from the putamen contralateral to the most affected side in the drug-naive group (p = 0.009), but not the levodopa-treated IPD groups compared with controls, There were no significant differences in NAA/(Cr+PCr) or Cho/(Cr+PCr) ratios. In untreated IPD, reduced putaminal NAA/Cho ratios may reflect loss of nigrostriatal dopamine terminals or alternatively indicate a functional abnormality of striatal putaminal neurons, such as membrane dysfunction due to striatal deafferentation. This study suggests that NAA/Cho ratios may be affected by L-dopa therapy and this may provide a reversible marker of neuronal dysfunction in the striatum.
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页码:438 / 444
页数:7
相关论文
共 26 条
[1]  
ARNOLD DL, 1992, 11TH P SMRM ANN M BE, P643
[2]   SPATIAL LOCALIZATION IN NMR-SPECTROSCOPY INVIVO [J].
BOTTOMLEY, PA .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 508 :333-348
[3]  
BRENNER RE, 1993, P 12 ANN M SOC MAGN, P1559
[4]   FUNCTIONAL IMAGING IN RELATION TO PARKINSONIAN SYNDROMES [J].
BROOKS, DJ .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1993, 115 (01) :1-17
[5]  
Chaudhuri K R, 1996, Parkinsonism Relat Disord, V2, P63, DOI 10.1016/1353-8020(96)00007-7
[6]  
CLARKE CE, 1996, MOV DISORD S1, V11, P103
[7]   A HYPOTHESIS ON THE PATHOPHYSIOLOGICAL MECHANISMS THAT UNDERLIE LEVODOPA-INDUCED OR DOPAMINE AGONIST-INDUCED DYSKINESIA IN PARKINSONS-DISEASE - IMPLICATIONS FOR FUTURE STRATEGIES IN TREATMENT [J].
CROSSMAN, AR .
MOVEMENT DISORDERS, 1990, 5 (02) :100-108
[8]   MAGNETIC-RESONANCE SPECTROSCOPIC STUDY OF PARKINSONISM RELATED TO BOXING [J].
DAVIE, CA ;
PIRTOSEK, Z ;
BARKER, GJ ;
KINGSLEY, DPE ;
MILLER, PH ;
LEES, AJ .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1995, 58 (06) :688-691
[9]   DIFFERENTIATION OF MULTIPLE SYSTEM ATROPHY FROM IDIOPATHIC PARKINSONS-DISEASE USING PROTON MAGNETIC-RESONANCE SPECTROSCOPY [J].
DAVIE, CA ;
WENNING, GK ;
BARKER, GJ ;
TOFTS, PS ;
KENDALL, BE ;
QUINN, N ;
MCDONALD, WI ;
MARSDEN, CD ;
MILLER, DH .
ANNALS OF NEUROLOGY, 1995, 37 (02) :204-210
[10]   PRIMATE MODELS OF MOVEMENT-DISORDERS OF BASAL GANGLIA ORIGIN [J].
DELONG, MR .
TRENDS IN NEUROSCIENCES, 1990, 13 (07) :281-285