Neuronal metabolic changes in the cortical region after subcortical infarction: a proton MR spectroscopy study

OBJECTIVES To investigate whether proton magnetic resonance spectroscopy (1H MRS) can detect neuronal metabolic changes in the cortical region in patients with cortical dysfunction after subcortical infarction. METHODS Fifteen patients with subcortical large (diameter⩾20 mm) infarcts were studied; n...

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Published inJournal of neurology, neurosurgery and psychiatry Vol. 69; no. 2; pp. 222 - 227
Main Authors Kang, Dong-Wha, Roh, Jae-Kyu, Lee, Yong-Seok, Song, In Chan, Yoon, Byung-Woo, Chang, Kee-Hyun
Format Journal Article
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Published London BMJ Publishing Group Ltd 01.08.2000
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Abstract OBJECTIVES To investigate whether proton magnetic resonance spectroscopy (1H MRS) can detect neuronal metabolic changes in the cortical region in patients with cortical dysfunction after subcortical infarction. METHODS Fifteen patients with subcortical large (diameter⩾20 mm) infarcts were studied; nine patients with cortical dysfunction (group A), and six without (group B). Seven patients with lacunar infarction served as controls. Infarct volume was measured on T2 weighted images with an image analyser. 1H MRS data were obtained in three regions; high signal intensity area on T2 weighted image, overlying cortex with a normal T2 MRI appearance, and contralateral homologous cortical region. RESULTS Infarct volume was not different between groups A and B. N-acetylaspartate (NAA)/creatine+phosphocreatine (Cr) ratios in the cortical region overlying subcortical infarcts in group A were significantly lower than those in group B and the control group (p=0.002). The NAA/Cr ratios in the overlying cortex were significantly lower than those in the contralateral normal cortex in group A on the initial (p=0.015) and follow up (p=0.028) 1H MRS, but these differences were not found in group B and the control group. CONCLUSIONS The results support the idea that the cerebral cortex is a responsible location for cortical dysfunction after subcortical infarctions.1H MRS can be used as a sensitive method for the detection of a neuronal metabolic damage, which is not demonstrated by conventional MRI.
AbstractList OBJECTIVES —To investigate whether proton magnetic resonance spectroscopy ( 1 H MRS) can detect neuronal metabolic changes in the cortical region in patients with cortical dysfunction after subcortical infarction.
 METHODS — Fifteen patients with subcortical large (diameter⩾20 mm) infarcts were studied; nine patients with cortical dysfunction (group A), and six without (group B). Seven patients with lacunar infarction served as controls. Infarct volume was measured on T2 weighted images with an image analyser. 1 H MRS data were obtained in three regions; high signal intensity area on T2 weighted image, overlying cortex with a normal T2 MRI appearance, and contralateral homologous cortical region.
 RESULTS —Infarct volume was not different between groups A and B. N-acetylaspartate (NAA)/creatine+phosphocreatine (Cr) ratios in the cortical region overlying subcortical infarcts in group A were significantly lower than those in group B and the control group (p=0.002). The NAA/Cr ratios in the overlying cortex were significantly lower than those in the contralateral normal cortex in group A on the initial (p=0.015) and follow up (p=0.028) 1 H MRS, but these differences were not found in group B and the control group.
 CONCLUSIONS —The results support the idea that the cerebral cortex is a responsible location for cortical dysfunction after subcortical infarctions. 1 H MRS can be used as a sensitive method for the detection of a neuronal metabolic damage, which is not demonstrated by conventional MRI.
To investigate whether proton magnetic resonance spectroscopy ((1)H MRS) can detect neuronal metabolic changes in the cortical region in patients with cortical dysfunction after subcortical infarction. Fifteen patients with subcortical large (diameter>/=20 mm) infarcts were studied; nine patients with cortical dysfunction (group A), and six without (group B). Seven patients with lacunar infarction served as controls. Infarct volume was measured on T2 weighted images with an image analyser. (1)H MRS data were obtained in three regions; high signal intensity area on T2 weighted image, overlying cortex with a normal T2 MRI appearance, and contralateral homologous cortical region. Infarct volume was not different between groups A and B. N-acetylaspartate (NAA)/creatine+phosphocreatine (Cr) ratios in the cortical region overlying subcortical infarcts in group A were significantly lower than those in group B and the control group (p=0.002). The NAA/Cr ratios in the overlying cortex were significantly lower than those in the contralateral normal cortex in group A on the initial (p=0. 015) and follow up (p=0.028) (1)H MRS, but these differences were not found in group B and the control group. The results support the idea that the cerebral cortex is a responsible location for cortical dysfunction after subcortical infarctions. (1)H MRS can be used as a sensitive method for the detection of a neuronal metabolic damage, which is not demonstrated by conventional MRI.
OBJECTIVES To investigate whether proton magnetic resonance spectroscopy (1 H MRS) can detect neuronal metabolic changes in the cortical region in patients with cortical dysfunction after subcortical infarction. METHODS Fifteen patients with subcortical large (diameter⩾20 mm) infarcts were studied; nine patients with cortical dysfunction (group A), and six without (group B). Seven patients with lacunar infarction served as controls. Infarct volume was measured on T2 weighted images with an image analyser. 1 H MRS data were obtained in three regions; high signal intensity area on T2 weighted image, overlying cortex with a normal T2 MRI appearance, and contralateral homologous cortical region. RESULTS Infarct volume was not different between groups A and B. N-acetylaspartate (NAA)/creatine+phosphocreatine (Cr) ratios in the cortical region overlying subcortical infarcts in group A were significantly lower than those in group B and the control group (p=0.002). The NAA/Cr ratios in the overlying cortex were significantly lower than those in the contralateral normal cortex in group A on the initial (p=0.015) and follow up (p=0.028) 1 H MRS, but these differences were not found in group B and the control group. CONCLUSIONS The results support the idea that the cerebral cortex is a responsible location for cortical dysfunction after subcortical infarctions.1 H MRS can be used as a sensitive method for the detection of a neuronal metabolic damage, which is not demonstrated by conventional MRI.
OBJECTIVES To investigate whether proton magnetic resonance spectroscopy (1H MRS) can detect neuronal metabolic changes in the cortical region in patients with cortical dysfunction after subcortical infarction. METHODS Fifteen patients with subcortical large (diameter⩾20 mm) infarcts were studied; nine patients with cortical dysfunction (group A), and six without (group B). Seven patients with lacunar infarction served as controls. Infarct volume was measured on T2 weighted images with an image analyser. 1H MRS data were obtained in three regions; high signal intensity area on T2 weighted image, overlying cortex with a normal T2 MRI appearance, and contralateral homologous cortical region. RESULTS Infarct volume was not different between groups A and B. N-acetylaspartate (NAA)/creatine+phosphocreatine (Cr) ratios in the cortical region overlying subcortical infarcts in group A were significantly lower than those in group B and the control group (p=0.002). The NAA/Cr ratios in the overlying cortex were significantly lower than those in the contralateral normal cortex in group A on the initial (p=0.015) and follow up (p=0.028) 1H MRS, but these differences were not found in group B and the control group. CONCLUSIONS The results support the idea that the cerebral cortex is a responsible location for cortical dysfunction after subcortical infarctions.1H MRS can be used as a sensitive method for the detection of a neuronal metabolic damage, which is not demonstrated by conventional MRI.
OBJECTIVESTo investigate whether proton magnetic resonance spectroscopy ((1)H MRS) can detect neuronal metabolic changes in the cortical region in patients with cortical dysfunction after subcortical infarction.METHODSFifteen patients with subcortical large (diameter>/=20 mm) infarcts were studied; nine patients with cortical dysfunction (group A), and six without (group B). Seven patients with lacunar infarction served as controls. Infarct volume was measured on T2 weighted images with an image analyser. (1)H MRS data were obtained in three regions; high signal intensity area on T2 weighted image, overlying cortex with a normal T2 MRI appearance, and contralateral homologous cortical region.RESULTSInfarct volume was not different between groups A and B. N-acetylaspartate (NAA)/creatine+phosphocreatine (Cr) ratios in the cortical region overlying subcortical infarcts in group A were significantly lower than those in group B and the control group (p=0.002). The NAA/Cr ratios in the overlying cortex were significantly lower than those in the contralateral normal cortex in group A on the initial (p=0. 015) and follow up (p=0.028) (1)H MRS, but these differences were not found in group B and the control group.CONCLUSIONSThe results support the idea that the cerebral cortex is a responsible location for cortical dysfunction after subcortical infarctions. (1)H MRS can be used as a sensitive method for the detection of a neuronal metabolic damage, which is not demonstrated by conventional MRI.
Author Chang, Kee-Hyun
Kang, Dong-Wha
Roh, Jae-Kyu
Song, In Chan
Yoon, Byung-Woo
Lee, Yong-Seok
AuthorAffiliation Department of Neurology, College of Medicine, Seoul National University, 28 Yongon-dong, Chongno-gu, Seoul 110-744, Korea
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Keywords Human
Cerebral infarction
Nervous system diseases
Cerebral cortex
Pathophysiology
Cardiovascular disease
Exploration
NMR spectrometry
Metabolism
Cerebral disorder
Vascular disease
Neuron
Central nervous system disease
Proton
Subcortex
Cerebrovascular disease
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Snippet OBJECTIVES To investigate whether proton magnetic resonance spectroscopy (1H MRS) can detect neuronal metabolic changes in the cortical region in patients with...
To investigate whether proton magnetic resonance spectroscopy ((1)H MRS) can detect neuronal metabolic changes in the cortical region in patients with cortical...
OBJECTIVES To investigate whether proton magnetic resonance spectroscopy (1 H MRS) can detect neuronal metabolic changes in the cortical region in patients...
OBJECTIVESTo investigate whether proton magnetic resonance spectroscopy ((1)H MRS) can detect neuronal metabolic changes in the cortical region in patients...
OBJECTIVES —To investigate whether proton magnetic resonance spectroscopy ( 1 H MRS) can detect neuronal metabolic changes in the cortical region in patients...
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StartPage 222
SubjectTerms Adult
Aged
Aged, 80 and over
Aphasia
Aspartic Acid - analogs & derivatives
Aspartic Acid - metabolism
Biological and medical sciences
Cerebral Angiography
Cerebral Cortex - blood supply
Cerebral Cortex - diagnostic imaging
Cerebral Cortex - metabolism
Cerebral Cortex - pathology
cerebral infarction
Cerebral Infarction - diagnosis
Cerebral Infarction - metabolism
Creatine - metabolism
Female
Humans
Image Processing, Computer-Assisted
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Male
Medical imaging
Medical sciences
Metabolism
Metabolites
Middle Aged
Neurology
Neurons - metabolism
Patients
Phosphocreatine - metabolism
Prospective Studies
Spectrum analysis
Studies
Tomography, Emission-Computed, Single-Photon
Tropical medicine
Vascular diseases and vascular malformations of the nervous system
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Title Neuronal metabolic changes in the cortical region after subcortical infarction: a proton MR spectroscopy study
URI http://dx.doi.org/10.1136/jnnp.69.2.222
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https://pubmed.ncbi.nlm.nih.gov/PMC1737068
Volume 69
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