Iron deposition and distribution across the hippocampus is associated with pattern separation and pattern completion in older adults at risk for Alzheimer’s disease
Open accessAbstract
Elevated iron deposition in the brain has been observed in older adult humans and persons with Alzheimer's disease (AD), and has been associated with lower cognitive performance. We investigated the impact of iron deposition, and its topographical distribution across hippocampal subfields and segments (anterior, posterior) measured along its longitudinal axis, on episodic memory in a sample of cognitively unimpaired older adults at elevated familial risk for AD (N = 172, 120 females, 52 males; mean age = 68.8 ± 5.4 years). MRI-based quantitative susceptibility maps were acquired to derive estimates of hippocampal iron deposition. The Mnemonic Similarity Task was used to measure pattern separation and pattern completion, two hippocampally mediated episodic memory processes. Greater hippocampal iron load was associated with lower pattern separation and higher pattern completion scores, both indicators of poorer episodic memory. Examination of iron levels within hippocampal subfields across its long axis revealed topographic specificity. Among the subfields and segments investigated here, iron deposition in the posterior hippocampal CA1 was the most robustly and negatively associated with the fidelity memory representations. This association remained after controlling for hippocampal volume and was observed in the context of normal performance on standard neuropsychological memory measures. These findings reveal that the impact of iron load on episodic memory performance is not uniform across the hippocampus. Both iron deposition levels as well as its spatial distribution, must be taken into account when examining the relationship between hippocampal iron and episodic memory in older adults at elevated risk for AD.
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The olfactory bulb is affected early in AD, playing an important role in the onset and progression of the disease.
“The OLF is affected early in AD, playing an important role in the onset and progression of the disease (Zhou et al., 2024).”
From Multimodal MRI combined with RNA sequencing reveals pathological signatures in the 9-month-old 3×Tg-AD mouse brain (2026) · cites this paper as Zhou et al., 2024
The Introduction and Discussion address early AD-related changes in the hippocampus, particularly iron deposition, but do not address the olfactory bulb. Searches for “olfactory bulb,” “OLF,” and early olfactory involvement in AD found no passage supporting the claim. Page numbers were not available in our copy. (LLM, conf=0.76)
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- Authors
- Zhou, J., Wearn, A., Huck, J., Hughes, C., Baracchini, G., Tremblay-Mercier, J., Poirier, J., Villeneuve, S., Tardif, C. L., Chakravarty, M. M., Daugherty, A. M., Gauthier, C. J., Turner, G. R., Spreng, R. N., & PREVENT-AD Research Group
- Affiliations
- Montreal Neurological Institute and Hospital (CA)
- Université de Sherbrooke (CA)
- Douglas Mental Health University Institute (CA)
- Wayne State University (US)
- Montreal Heart Institute (CA)
- York University (CA)
- ORCID
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2024-02-22
- Volume
- 44
- Issue
- 19
- Pages
- e1973232024
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC11079967
- OpenAlex
- W4392028257
- Cited by
- 20
- References
- 7
- Citations by year
- 2026: 8 · 2025: 8 · 2024: 4
- FWCI
- 5.88
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- HHS | NIH | National Institute on Aging (R01AG068563)
- Alzheimer's Association (AARG-22-927100)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Neurology › Neurological diseases and metabolism
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Keywords
- pattern separation, pattern completion, episodic memory, Alzheimer's disease risk, quantitative susceptibility mapping, hippocampal subfields, CA1, older adults, memory fidelity
- MeSH terms
- Aged, Alzheimer Disease, Female, Hippocampus, Humans, Iron, Magnetic Resonance Imaging, Male, Middle Aged, Memory, Episodic
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