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The profile of hippocampal metabolites differs between Alzheimers disease and subcortical ischemic vascular dementia as measured by proton magnetic resonance spectroscopy

机译:质子磁共振波谱测定阿尔茨海默氏病和皮层下缺血性血管性痴呆的海马代谢产物特征不同

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摘要

Alzheimer's disease (AD) and subcortical ischemic vascular dementia (SIVD) have overlapping pathologies and risk factors, but their underlying neurodegenerative mechanisms are basically different. We performed magnetic resonance spectroscopy (MRS) to study metabolite differences between the two diseases in vivo. The subjects were 31 patients with SIVD and 99 with AD. Additionally, 45 elderly subjects were recruited as controls. We measured N-acetylaspartate (NAA), glutamine and glutamate (Glx), and myoinositol (mIns) concentration quantitatively using a 1.5-T MR scanner. N-acetylaspartate and Glx concentrations decreased in the hippocampus and cingulate/precuneal cortices (PCC) in both AD and SIVD patients, and the NAA decrease in the hippocampus was more prominent in AD than in SIVD. Interestingly, the pattern of mIns concentration changes differed between the two disorders; mIns was increased in AD but not increased in SIVD. If one differentiates between AD and SIVD by the mIns concentration in the hippocampus, the area under the receiver operating characteristic curve was 0.95, suggesting a high potential for discrimination. Our results suggest that proton MRS can provide useful information to differentiate between AD and SIVD. The difference of mIns concentrations in the hippocampus and PCC seems to reflect the different neurodegenerative mechanisms of the two disorders.
机译:阿尔茨海默氏病(AD)和皮层下缺血性血管性痴呆(SIVD)具有重叠的病理和危险因素,但其潜在的神经退行性机制却基本不同。我们进行了磁共振波谱(MRS),以研究体内两种疾病之间的代谢物差异。受试者为31例SIVD患者和99例AD患者。另外,招募了45名老年受试者作为对照。我们使用1.5-T MR扫描仪定量测量了N-乙酰天门冬氨酸(NAA),谷氨酰胺和谷氨酸(Glx)和肌醇(mIns)浓度。在AD和SIVD患者中,海马和扣带回/乳突皮质(PCC)中N-乙酰天门冬氨酸和Glx的浓度降低,而AD中海马的NAA降低比在SIVD中更为明显。有趣的是,两种疾病之间的mIns浓度变化模式有所不同。 AD的mIns增加,而SIVD的mIns没有增加。如果通过海马中的mIns浓度区分AD和SIVD,则接受者工作特征曲线下方的面积为0.95,表明存在很高的辨别力。我们的结果表明质子MRS可以提供​​有用的信息来区分AD和SIVD。海马和PCC中mIns浓度的差异似乎反映了这两种疾病的不同神经退行性机制。

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