Evidence map›Paper›PMID 42859279›Full record

ArticleBrain imaging and behavior2026

Characterizing hippocampal activation during pattern separation with multi-echo fMRI in cognitively normal older adults.

Kevin Grant Solar, Sriranga Kashyap, Nicolas Deom, Kâmil Uludağ, Ljubica Zotovic, Krista Lanctôt, Sandra E Black, Mary Pat McAndrews

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Article in Brain imaging and behavior, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Kevin Grant SolarDivision of Clinical & Computational Neuroscience, Krembil Brain Institute, University Health Network, 399 Bathurst Street, Toronto, ON, M5T 2S8, Canada.ORCID http://orcid.org/0000-0002-4072-6645
Sriranga KashyapDivision of Brain, Imaging & Behaviour, Krembil Brain Institute, University Health Network, 399 Bathurst Street, Toronto, ON, M5T 2S8, Canada.
Nicolas DeomDivision of Clinical & Computational Neuroscience, Krembil Brain Institute, University Health Network, 399 Bathurst Street, Toronto, ON, M5T 2S8, Canada.
Kâmil UludağDivision of Brain, Imaging & Behaviour, Krembil Brain Institute, University Health Network, 399 Bathurst Street, Toronto, ON, M5T 2S8, Canada.
Ljubica ZotovicDivision of Neurology, Department of Medicine, Sunnybrook Research Institute, University of Toronto, 2075 Bayview Avenue, Toronto, ON, M4N 3M5, Canada.
Krista LanctôtEvaluative Clinical Sciences, Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, Departments of Psychiatry and Pharmacology and Toxicology, University of Toronto, 2075 Bayview Avenue, Toronto, ON, M4N 3M5, Canada.
Sandra E BlackDivision of Neurology, Department of Medicine, Sunnybrook Research Institute, University of Toronto, 2075 Bayview Avenue, Toronto, ON, M4N 3M5, Canada.
Mary Pat McAndrewsDivision of Clinical & Computational Neuroscience, Krembil Brain Institute, University Health Network, 399 Bathurst Street, Toronto, ON, M5T 2S8, Canada. Mary.McAndrews@uhn.ca.

Funding

Weston Family Foundation CT200401
6 · The paper itself

Abstract

Hippocampal hyperactivity, detected with mnemonic similarity task (MST) fMRI, is both a promising marker of risk and a probable driver of degeneration in Alzheimer's disease (AD). However, implementation of such fMRI in interventional research is limited by long scan times and the absence of a framework for identifying prospective participants with hyperactivity who could be targeted with therapeutic approaches aimed at reducing this activity. We used multi-echo fMRI during the MST, an episodic memory task previously shown to engage hippocampal subfields CA3 and dentate gyrus (DG), to characterize activity profiles in 33 cognitively normal older adults. We compared MST-related CA3 and DG activation and behavioural performance across subsets of eight task runs. Behavioural and activation effects were equivalent for the first set of four runs (Runs-A) and the second set (Runs-B), suggesting that robust data can be obtained with four runs. Left and right CA3 + DG activation did not differ. We provide an exemplar framework for the derivation of a threshold for single-participant classification of elevated hippocampal activation as an indicator of AD risk in cognitively normal older individuals. Scalable (~22 min) multi-echo MST fMRI robustly captures hippocampal activation and provides a framework for individual-level characterization of hippocampal function in cognitively normal older adults. This enables individualized detection of elevated hippocampal activation as a modifiable risk factor and may guide enrolment into prevention trials targeting preclinical AD.

Indexed as

CognitionHippocampusMagnetic Resonance ImagingAgedAged, 80 and overAgingAlzheimer DiseaseBrain MappingDentate GyrusFemaleHumansImage Processing, Computer-AssistedMaleMemory, EpisodicNeuropsychological TestsFunctional MRIHippocampusMemoryMnemonic similarity taskPreclinical Alzheimer’s disease

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.