Hippocampal subfield volumetry in patients with subcortical vascular mild cognitive impairment

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作者
Xinwei Li
Deyu Li
Qiongling Li
Yuxia Li
Kuncheng Li
Shuyu Li
Ying Han
机构
[1] Key Laboratory for Biomechanics and Mechanobiology of the Ministry of Education,Department of Neurology
[2] School of Biological Science & Medical Engineering,Department of Neurology
[3] Beihang University,Department of Radiology
[4] Center of Alzheimer’s Disease,undefined
[5] Beijing Institute for Brain Disorders,undefined
[6] Xuan Wu Hospital,undefined
[7] Capital Medical University,undefined
[8] Tangshan Gongren Hospital,undefined
[9] Xuan Wu Hospital,undefined
[10] Capital Medical University,undefined
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摘要
Memory impairment is a typical characteristic of patients with subcortical vascular mild cognitive impairment (svMCI) or with amnestic mild cognitive impairment (aMCI). The hippocampus, which plays an important role in the consolidation of information from short-term memory to long-term memory, is a heterogeneous structure that consists of several anatomically and functionally distinct subfields. However, whether distinct hippocampal subfields are differentially and selectively affected by svMCI pathology and whether these abnormal changes in hippocampal subfields are different between svMCI and aMCI patients are largely unknown. A total of 26 svMCI patients, 26 aMCI patients and 26 healthy controls matched according to age, gender and years of education were enrolled in this study. We utilized an automated hippocampal subfield segmentation method provided by FreeSurfer to estimate the volume of several hippocampal subfields, including the cornu ammonis (CA) areas, the dentate gyrus (DG), the subiculum and the presubiculum. Compared with controls, the left subiculum and presubiculum and the right CA4/DG displayed significant atrophy in patients with svMCI. Interestingly, we also found significant differences in the volume of the right CA1 between the svMCI and aMCI groups. Taken together, our results reveal region-specific vulnerability of hippocampal subfields to svMCI pathology and identify distinct hippocampal subfield atrophy patterns between svMCI and aMCI patients.
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