Alzheimer’s disease and the fornix

Alzheimer’s disease (AD) is the most common form of neurodegenerative dementia. Researchers have long been focused on the cortical pathology of AD, since the most important pathologic features are the senile plaques found in the cortex, and the neurofibrillary tangles and neuronal loss that begin in...

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Main Authors: Kenichi eOishi, Constantine eLyketsos
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-09-01
Series:Frontiers in Aging Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnagi.2014.00241/full
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author Kenichi eOishi
Constantine eLyketsos
Constantine eLyketsos
Constantine eLyketsos
author_facet Kenichi eOishi
Constantine eLyketsos
Constantine eLyketsos
Constantine eLyketsos
author_sort Kenichi eOishi
collection DOAJ
description Alzheimer’s disease (AD) is the most common form of neurodegenerative dementia. Researchers have long been focused on the cortical pathology of AD, since the most important pathologic features are the senile plaques found in the cortex, and the neurofibrillary tangles and neuronal loss that begin in the entorhinal cortex and the hippocampus. In addition to these gray matter structures, histopathological studies indicate that the white matter is also a good target for both the early diagnosis of AD and for monitoring disease progression. The fornix is a white matter bundle that constitutes a core element of the limbic circuits, and is one of the most important anatomical structures related to memory. Functional and anatomical features of the fornix have naturally captured researchers’ attention as possible diagnostic and prognostic markers of AD. Indeed, neurodegeneration of the fornix has been histologically observed in AD, and growing evidence indicates that the alterations seen in the fornix are potentially a good marker to predict future conversion from mild cognitive impairment to AD, and even from cognitively normal individuals to AD. The degree of alteration is correlated with the degree of memory impairment, indicating the potential for the use of the fornix as a functional marker. Moreover, there have been attempts to stimulate the fornix using deep brain stimulation (DBS) to augment cognitive function in AD, and ongoing research has suggested positive effects of DBS on brain glucose metabolism in AD patients. On the other hand, disease specificity for fornix degeneration, methodologies to evaluate fornix degeneration, and the clinical significance of the fornix DBS, especially for the long-term impact on the quality of life, are mostly unknown and need to be elucidated.
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spelling doaj.art-d8614296a3de47699611d2ca87764fa12022-12-21T19:16:31ZengFrontiers Media S.A.Frontiers in Aging Neuroscience1663-43652014-09-01610.3389/fnagi.2014.00241108744Alzheimer’s disease and the fornixKenichi eOishi0Constantine eLyketsos1Constantine eLyketsos2Constantine eLyketsos3Johns Hopkins UniversityJohns Hopkins UniversityJohns Hopkins HospitalJohns Hopkins Bayview Medical CenterAlzheimer’s disease (AD) is the most common form of neurodegenerative dementia. Researchers have long been focused on the cortical pathology of AD, since the most important pathologic features are the senile plaques found in the cortex, and the neurofibrillary tangles and neuronal loss that begin in the entorhinal cortex and the hippocampus. In addition to these gray matter structures, histopathological studies indicate that the white matter is also a good target for both the early diagnosis of AD and for monitoring disease progression. The fornix is a white matter bundle that constitutes a core element of the limbic circuits, and is one of the most important anatomical structures related to memory. Functional and anatomical features of the fornix have naturally captured researchers’ attention as possible diagnostic and prognostic markers of AD. Indeed, neurodegeneration of the fornix has been histologically observed in AD, and growing evidence indicates that the alterations seen in the fornix are potentially a good marker to predict future conversion from mild cognitive impairment to AD, and even from cognitively normal individuals to AD. The degree of alteration is correlated with the degree of memory impairment, indicating the potential for the use of the fornix as a functional marker. Moreover, there have been attempts to stimulate the fornix using deep brain stimulation (DBS) to augment cognitive function in AD, and ongoing research has suggested positive effects of DBS on brain glucose metabolism in AD patients. On the other hand, disease specificity for fornix degeneration, methodologies to evaluate fornix degeneration, and the clinical significance of the fornix DBS, especially for the long-term impact on the quality of life, are mostly unknown and need to be elucidated.http://journal.frontiersin.org/Journal/10.3389/fnagi.2014.00241/fullDiffusion Tensor ImagingLimbic SystemMagnetic Resonance ImagingMild Cognitive ImpairmentAlzheimer’s diseasedeep brain stimulation (DBS)
spellingShingle Kenichi eOishi
Constantine eLyketsos
Constantine eLyketsos
Constantine eLyketsos
Alzheimer’s disease and the fornix
Frontiers in Aging Neuroscience
Diffusion Tensor Imaging
Limbic System
Magnetic Resonance Imaging
Mild Cognitive Impairment
Alzheimer’s disease
deep brain stimulation (DBS)
title Alzheimer’s disease and the fornix
title_full Alzheimer’s disease and the fornix
title_fullStr Alzheimer’s disease and the fornix
title_full_unstemmed Alzheimer’s disease and the fornix
title_short Alzheimer’s disease and the fornix
title_sort alzheimer s disease and the fornix
topic Diffusion Tensor Imaging
Limbic System
Magnetic Resonance Imaging
Mild Cognitive Impairment
Alzheimer’s disease
deep brain stimulation (DBS)
url http://journal.frontiersin.org/Journal/10.3389/fnagi.2014.00241/full
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