Cited by 181Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsMemory and Neural Mechanisms

Hippocampal CA1 apical neuropil atrophy and memory performance in Alzheimer's disease

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Kerchner, Geoffrey A., Deutsch, Gayle K., Zeineh, Michael, Dougherty, Robert F., Saranathan, Manojkumar, Rutt, Brian K.·2012·NeuroImage

Abstract

Memory loss is often the first and most prominent symptom of Alzheimer's disease (AD), coinciding with the spread of neurofibrillary pathology from the entorhinal cortex (ERC) to the hippocampus. The apical dendrites of hippocampal CA1 pyramidal neurons, in the stratum radiatum/stratum lacunosum-moleculare (SRLM), are among the earliest targets of this pathology, and atrophy of the CA1-SRLM is apparent in postmortem tissue from patients with mild AD. We previously demonstrated that CA1-SRLM thinning is also apparent in vivo, using ultra-high field 7-Tesla (7T) MRI to obtain high-resolution hippocampal microstructural imaging. Here, we hypothesized that CA1-SRLM thickness would correlate with episodic memory performance among patients with mild AD. We scanned nine patients, using an oblique coronal T2-weighted sequence through the hippocampal body with an in-plane resolution of 220 μm, allowing direct visual identification of subfields - dentate gyrus (DG)/CA3, CA2, CA1, and ERC - and hippocampal strata - SRLM and stratum pyramidale (SP). We present a novel semi-automated method of measuring stratal width that correlated well with manual measurements. We performed multi-domain neuropsychological evaluations that included three tests of episodic memory, yielding composite scores for immediate recall, delayed recall, and delayed recognition memory. Strong correlations occurred between delayed recall performance and the widths of CA1-SRLM (r(2)=0.69; p=0.005), CA1-SP (r(2)=0.5; p=0.034), and ERC (r(2)=0.62; p=0.012). The correlation between CA1-SRLM width and delayed recall lateralized to the left hemisphere. DG/CA3 size did not correlate significantly with any aspect of memory performance. These findings highlight a role for 7T hippocampal microstructural imaging in revealing focal structural pathology that correlates with the central cognitive feature of AD.

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Authors
Kerchner, G. A., Deutsch, G. K., Zeineh, M., Dougherty, R. F., Saranathan, M., & Rutt, B. K.
Affiliations
  • Stanford Medicine (US)
  • Stanford University (US)
Corresponding author
Kerchner, Geoffrey A.
Venue
NeuroImage
Publisher
Elsevier BV
Published
2012-10
Volume
63
Issue
1
Pages
194-202
ISSN
1053-8119 (ISSN-L)
OpenAlex
W1971640012
Cited by
181
References
5
Citations by year
2026: 13 · 2025: 9 · 2024: 10 · 2023: 8 · 2022: 21 · 2021: 10 · 2020: 16 · 2019: 14 · 2018: 13 · 2017: 15 · 2016: 14 · 2015: 12 · 2014: 16 · 2013: 10
FWCI
8.22
Type
journal article
Language
en
Open access
Locations
  • NeuroImage (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Alzheimer's Association (NIRG-11-205493)
  • NIH (P41 RR09784)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords
Alzheimer's disease, hippocampal CA1, apical dendrites, hippocampal microstructure, episodic memory, delayed recall, entorhinal cortex, neurofibrillary pathology, 7T MRI, hemispheric lateralization
MeSH terms
Aged, Aged, 80 and over, Alzheimer Disease, Atrophy, Female, Hippocampus, Humans, Magnetic Resonance Imaging, Male, Memory Disorders, Middle Aged, Mental Recall, Neuropil

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