Quantitative 1H-MRS of healthy human cortex, hippocampus, and thalamus:: Metabolite concentrations, quantification precision, and reproducibility

被引:62
作者
Geurts, JJG
Barkhof, F
Castelijns, JA
Uitdehaag, BMJ
Polman, CH
Pouwels, PJW
机构
[1] Vrije Univ Amsterdam, Ctr Med, Dept Phys & Med Technol, MR Ctr MS Res, NL-1081 HV Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Ctr Med, Dept Radiol, MR Ctr MS Res, NL-1081 HV Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Ctr Med, Dept Neurol, MR Ctr MS Res, NL-1081 HV Amsterdam, Netherlands
关键词
magnetic resonance spectroscopy; gray matter; reproducibility; quantification precision; CoV; error estimate;
D O I
10.1002/jmri.20138
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 [临床医学]; 100207 [影像医学与核医学]; 1009 [特种医学];
摘要
Purpose: To evaluate metabolite concentrations in cortical gray matter, hippocampus, and thalamus of healthy adults, and to investigate precision and reproducibility of quantitative proton magnetic resonance spectroscopy (H-1-MRS) in these gray matter regions. Materials and Methods: Quantitative single-voxel short echo-time spectra were obtained from healthy human cortex, hippocampus, and thalamus. Subjects were examined twice. Metabolite concentrations, quantification precision, and reproducibility were determined. Results: There were no significant differences between test and retest measurements. Regional differences were observed with respect to metabolite concentrations, quantification precision, and reproducibility. Quantification precision and reproducibility of N-acetylaspartate and N-acetyl aspartylglutamate (tNAA), creatine and phosphocreatine (tCr), choline-containing compounds (Cho), and myo-inositol (myo-Ins), were better than those of glutamate (Glu) and glutamine (Gln). Generally, precision and reproducibility were better in cortex than in hippocampus or thalamus. The quantification precision was shown to correlate both with reproducibility and spectral linewidth. Conclusion: The reliability of quantitative MRS depends on the metabolite concerned, its concentration, and on the brain area studied. Moreover, the quantification precision of a metabolite in a single spectrum appears to be a reliable measure for its reproducibility in a longitudinal study.
引用
收藏
页码:366 / 371
页数:6
相关论文
共 45 条
[1]
Bartha R, 2000, MAGNET RESON MED, V44, P185, DOI 10.1002/1522-2594(200008)44:2<185::AID-MRM4>3.0.CO
[2]
2-V
[3]
Prediction of neuropsychological impairment in multiple sclerosis - Comparison of conventional magnetic resonance imaging measures of atrophy and lesion burden [J].
Benedict, RHB ;
Weinstock-Guttman, B ;
Fishman, I ;
Sharma, J ;
Tjoa, CW ;
Bakshi, R .
ARCHIVES OF NEUROLOGY, 2004, 61 (02) :226-230
[4]
Acute axonal injury in multiple sclerosis -: Correlation with demyelination and inflammation [J].
Bitsch, A ;
Schuchardt, J ;
Bunkowski, S ;
Kuhlmann, T ;
Brück, W .
BRAIN, 2000, 123 :1174-1183
[5]
Axonal pathology in myelin disorders [J].
Bjartmar, C ;
Yin, XH ;
Trapp, BD .
JOURNAL OF NEUROCYTOLOGY, 1999, 28 (4-5) :383-395
[6]
Cortical cerebral metabolism correlates with MRI lesion load and cognitive dysfunction in MS [J].
Blinkenberg, M ;
Rune, K ;
Jensen, CV ;
Ravnborg, M ;
Kyllingsbæk, S ;
Holm, S ;
Paulson, OB ;
Sorensen, PS .
NEUROLOGY, 2000, 54 (03) :558-564
[7]
Brooks WM, 1999, MAGNET RESON MED, V41, P193, DOI 10.1002/(SICI)1522-2594(199901)41:1<193::AID-MRM27>3.0.CO
[8]
2-P
[9]
Reproducibility of in vivo metabolite quantification with proton magnetic resonance spectroscopic Imaging [J].
Chard, DT ;
McLean, MA ;
Parker, GJM ;
MacManus, DG ;
Miller, DH .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2002, 15 (02) :219-225
[10]
Choi CG, 1999, MAGNET RESON MED, V41, P204, DOI 10.1002/(SICI)1522-2594(199901)41:1<204::AID-MRM29>3.0.CO