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为什么仅仅观察整个海马体是不够的——前后轴、亚区和激活分析在提高海马体变化对阿尔茨海默病诊断的预测价值方面的关键作用。

Why looking at the whole hippocampus is not enough-a critical role for anteroposterior axis, subfield and activation analyses to enhance predictive value of hippocampal changes for Alzheimer's disease diagnosis.

机构信息

Centre for the Cellular Basis of Behaviour, Department of Neuroscience, Institute of Psychiatry, King's College London London, UK.

出版信息

Front Cell Neurosci. 2014 Mar 31;8:95. doi: 10.3389/fncel.2014.00095. eCollection 2014.

Abstract

The hippocampus is one of the earliest affected brain regions in Alzheimer's disease (AD) and its dysfunction is believed to underlie the core feature of the disease-memory impairment. Given that hippocampal volume is one of the best AD biomarkers, our review focuses on distinct subfields within the hippocampus, pinpointing regions that might enhance the predictive value of current diagnostic methods. Our review presents how changes in hippocampal volume, shape, symmetry and activation are reflected by cognitive impairment and how they are linked with neurogenesis alterations. Moreover, we revisit the functional differentiation along the anteroposterior longitudinal axis of the hippocampus and discuss its relevance for AD diagnosis. Finally, we indicate that apart from hippocampal subfield volumetry, the characteristic pattern of hippocampal hyperactivation associated with seizures and neurogenesis changes is another promising candidate for an early AD biomarker that could become also a target for early interventions.

摘要

海马体是阿尔茨海默病(AD)最早受影响的大脑区域之一,其功能障碍被认为是该疾病核心特征——记忆损伤的基础。鉴于海马体体积是 AD 的最佳生物标志物之一,我们的综述重点关注了海马体内部的不同子区域,指出了可能增强当前诊断方法预测价值的区域。我们的综述介绍了海马体体积、形状、对称性和激活的变化如何反映认知障碍,以及它们与神经发生变化的关系。此外,我们重新审视了海马体沿前后轴的功能分化,并讨论了其对 AD 诊断的相关性。最后,我们指出,除了海马体子区域体积测量,与癫痫和神经发生变化相关的海马体过度激活特征模式也是 AD 早期生物标志物的另一个有前途的候选者,它也可能成为早期干预的目标。

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