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摘要
Background: In Alzheimer%26apos;s disease (AD), levels of N-acetylaspartate (NAA) is diminished and choline (Cho) and myo-inositol (mI) are increased. In cerebrospinal fluid (CSF), tau and phosphoylated tau (p-tau(181P)) is increased and amyloid-beta(1-42) (A beta(42)) decreased. %26lt;br%26gt;Objectives: 1) To compare metabolites of different H-1-MRS voxels and assess its utility to differentiate AD from controls and to examine the relationship to cognition and to CSF markers. %26lt;br%26gt;Methods: 17 healthy controls and 19 AD subjects were studied using H-1-MRS. In the AD cases, additional CSF analysis was obtained. %26lt;br%26gt;Results: Relative to controls, AD subjects had reduced NAA/Creatine (Cr) levels in hippocampus (42.3% to 26.0%, p %26lt; 0.001), posterior cingulate gyrus (10.4% to 0.2%, p = 0.04), and parietal lobe (14.9% to 3.8%, p = 0.002). Further differences of Cho/Cr and mI/Cr in the hippocampus (Cho/Cr: p = 0.04; mI/Cr: p = 0.015) and posterior cingulate (Cho/Cr: p = 0.001; mI/Cr: p = 0.001) were observed. NAA/Cr of the hippocampus yielded the highest sensitivity (94.1%) and specificity (92.3%) to differentiate AD from controls. NAA/Cr was associated with general cognition (hippocampus: R = 0.68, p %26lt; 0.001; parietal lobe: R = 0.57, p = 0.001; posterior cingulate: R = 0.50, p = 0.003). Higher hippocampal NAA/Cr was related to higher CSF A beta(42), while lower parietal NAA/Cr was associated with a higher CSF total tau (t-tau) and p-tau(181P). Posterior cingulate mI/Cr was related to CSF t-tau and NAA/mI. %26lt;br%26gt;Conclusion: H-1-MRS is an appropriate measure in AD. Measurement at different regions presumably reflects different pathological changes.
- 出版日期2013
