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Published on: July 19, 2019
Reduced N-acetylaspartate is consistent with axonal dysfunction in cerebral small vessel disease
Arani Nitkunan1, Rebecca A Charlton, Thomas R Barrick
1Centre for Clinical Neuroscience, St George's, University of London, London, UK. a.nitkunan@sgul.ac.uk
NMR in Biomedicine
|November 15, 2008
Summary
Cerebral small vessel disease (SVD) shows reduced N-acetylaspartate (NAA), a neuronal marker, but this change is linked to lesion load, not cognition. Magnetic resonance spectroscopy (MRS) is not a reliable surrogate marker for SVD disease progression.
Area of Science:
- Neuroimaging
- Neurology
- Biochemistry
Background:
- Cerebral small vessel disease (SVD) is a significant contributor to cognitive impairment, yet its underlying pathological mechanisms require further elucidation.
- Investigating brain metabolic alterations in SVD patients compared to controls is crucial for understanding disease progression.
Purpose of the Study:
- To utilize proton magnetic resonance spectroscopy (1H MRS) for assessing brain metabolic differences in SVD patients.
- To correlate observed metabolic changes with cognitive function in individuals with SVD.
Main Methods:
- Multi-voxel spectroscopic imaging of white matter was performed on 29 SVD patients and 35 controls.
- Absolute metabolite concentrations (N-acetylaspartate, creatines, cholines, myo-inositol, lactate) were quantified.
- Cognitive tests were administered to SVD patients, and composite scores were calculated.
Main Results:
- A significant reduction in N-acetylaspartate (NAA) was observed in SVD patients compared to controls (7.27% decrease, P=0.004).
- This NAA reduction was primarily attributed to lesion load within voxels, losing significance when adjusted for lesion volume (22% in SVD vs. 5% in controls, P<0.001).
- No significant correlation was found between cognitive scores and brain metabolite levels in SVD patients. Lactate was not detected.
Conclusions:
- The primary metabolic alteration in SVD is a decrease in NAA, indicating compromised neuronal integrity.
- The absence of correlation between NAA levels and cognitive performance suggests MRS is not a suitable surrogate marker for SVD.
- Further research is needed to fully understand the pathophysiology of SVD and its impact on cognition.
