Hippocampal CA1 apical neuropil atrophy and memory performance in Alzheimer's disease
Open accessAbstract
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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CA1/CA2 neurons are vulnerable to AD pathology.
“This was particularly evident in CA1/CA2 neurons, which are vulnerable to AD pathology. 58”
From Disruption of hippocampal upstream regulators of mTOR and insulin pathways in Down syndrome with Alzheimer's disease neuropathology: Preliminary observations (2026) · cites this paper as [58]
The Introduction (page unavailable) describes the CA1 apical neuropil as especially vulnerable to early AD pathology and says pathology there precedes loss of CA1 pyramidal neurons. The paper does not establish that CA2 neurons are vulnerable; its mention of CA2 in Methods concerns anatomical boundaries. (LLM, conf=0.87)
Experimental — accuracy not yet measuredThe increase in C1QB RNA expression was particularly evident in CA1/CA2 neurons.
“This was particularly evident in CA1/CA2 neurons, which are vulnerable to AD pathology. 58”
From Disruption of hippocampal upstream regulators of mTOR and insulin pathways in Down syndrome with Alzheimer's disease neuropathology: Preliminary observations (2026) · cites this paper as [58]
The Introduction describes the CA1 apical neuropil as especially vulnerable to early Alzheimer’s disease pathology, supporting the sentence’s point about CA1. Our copy does not address CA2 vulnerability or report C1QB RNA expression, so it does not support the full claim. (LLM, conf=0.85)
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“58 Our findings support a hyperactivated AKT/mTOR/p70S6K axis with IRS1 inhibition in humans with DS-AD.”
- 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.
- ORCID
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2012-10
- Volume
- 63
- Issue
- 1
- Pages
- 194-202
- ISSN
- 1053-8119 (ISSN-L)
- PMC
- PMC3677969
- 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
- green
- www.ncbi.nlm.nih.gov
- 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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