TY - JOUR
T1 - Characterization of cerebral small vessel disease by proton spectroscopy and morphological magnetic resonance
AU - Hund-Georgiadis, Margret
AU - Norris, David G.
AU - Guthke, Thomas
AU - Von Cramon, D. Yves
PY - 2001
Y1 - 2001
N2 - This study sought to investigate whether clinical and neuropsychological impairment in cerebral small vessel disease (CSVD) can be evaluated by proton spectroscopy (1H-MRS) and structural magnetic resonance (MR) imaging. Sixteen patients with CSVD and 15 healthy age-matched controls participated in the study. In addition to spectroscopic and structural MR examination all patients underwent a comprehensive clinical and neuropsychological investigation. Significant differences in between patients and controls were revealed by 1H-MRS in the parietal white matter: decreased metabolic ratios of N-acetyl aspartate to choline (NAA/Cho; patients: 1.37 ± 0.17, control: 1.72 ± 0.25, p < 0.001) and of N-acetyl aspartate to creatin (NAA/Cr; patients: 1.41 ± 0.15, control: 1.66 ± 0.2, p < 0.01) indicated a pathological state. Evaluation of spectroscopic and neuropsychological data revealed a close relation between attentional impairment, i.e. delayed cerebral transmission time and decreased NAA/Cho and NAA/Cr (r = 0.62, p = 0.014). In sum, 1H-MRS allowed a clear discrimination between patients with CSVD and age-matched normal controls. Moreover, comparisons of 1H-MRS and neuropsychological data suggested that NAA metabolic levels, and particularly the delay in cerebral transmission time, could be potential predictors of the severeness of attentional impairment.
AB - This study sought to investigate whether clinical and neuropsychological impairment in cerebral small vessel disease (CSVD) can be evaluated by proton spectroscopy (1H-MRS) and structural magnetic resonance (MR) imaging. Sixteen patients with CSVD and 15 healthy age-matched controls participated in the study. In addition to spectroscopic and structural MR examination all patients underwent a comprehensive clinical and neuropsychological investigation. Significant differences in between patients and controls were revealed by 1H-MRS in the parietal white matter: decreased metabolic ratios of N-acetyl aspartate to choline (NAA/Cho; patients: 1.37 ± 0.17, control: 1.72 ± 0.25, p < 0.001) and of N-acetyl aspartate to creatin (NAA/Cr; patients: 1.41 ± 0.15, control: 1.66 ± 0.2, p < 0.01) indicated a pathological state. Evaluation of spectroscopic and neuropsychological data revealed a close relation between attentional impairment, i.e. delayed cerebral transmission time and decreased NAA/Cho and NAA/Cr (r = 0.62, p = 0.014). In sum, 1H-MRS allowed a clear discrimination between patients with CSVD and age-matched normal controls. Moreover, comparisons of 1H-MRS and neuropsychological data suggested that NAA metabolic levels, and particularly the delay in cerebral transmission time, could be potential predictors of the severeness of attentional impairment.
KW - Cerebral small vessel disease
KW - Cholin
KW - Cognitive impairment
KW - N-acetyl aspartate
KW - Proton spectroscopy
KW - NLA
UR - http://www.scopus.com/inward/record.url?scp=0034894645&partnerID=8YFLogxK
U2 - 10.1159/000047686
DO - 10.1159/000047686
M3 - Article
C2 - 11490101
AN - SCOPUS:0034894645
SN - 1015-9770
VL - 12
SP - 82
EP - 90
JO - Cerebrovascular diseases
JF - Cerebrovascular diseases
IS - 2
ER -