# Spatial pattern separation deficits in early Alzheimer’s disease are comparable in humans and animal models

**Authors:** Martina Laczó, Kristyna Maleninska, Natalie Khazaalova, Sarka Borovska, Martin Vyhnalek, Jakub Hort, Ales Stuchlik, Jan Svoboda, Jan Laczó

PMC · DOI: 10.1038/s41598-026-36266-y · 2026-01-22

## TL;DR

This study shows that spatial pattern separation deficits in early Alzheimer's disease are similar in humans and animal models, suggesting a useful tool for translational research.

## Contribution

The study demonstrates that spatial pattern separation deficits are comparable in humans and animal models of early Alzheimer's disease.

## Key findings

- AD aMCI participants performed worse than cognitively normal participants in spatial pattern separation tasks.
- TgF344-AD rats performed worse than wild-type rats in a 90° spatial pattern separation probe trial.
- SPS deficits in early AD are not due to general memory impairment and are comparable across species.

## Abstract

Spatial pattern separation (SPS) is a memory process that enables the discrimination of similar spatial locations. This process is vulnerable to pathophysiological changes in the early stages of Alzheimer’s disease (AD), but the translational potential of its testing remains unclear. This study aimed to evaluate the potential of SPS testing as a translational cognitive marker for identifying early AD and enabling direct comparisons of cognitive outcomes in animals and humans. We used a validated SPS task to examine biomarker-defined participants with amnestic mild cognitive impairment due to AD (AD aMCI; n = 56) and cognitively normal (CN) participants (n = 60). An animal version of this task, based on a modified Morris Water Maze task, was used to test six-month-old transgenic TgF344-AD rats (n = 38) and wild-type (WT) rats (n = 36). AD aMCI participants performed worse than CN participants, with performance declining as distance decreased. These results remained unchanged when adjusted for memory performance. TgF344-AD rats performed worse than WT rats in a probe trial with a 90° SPS design, but not in probe trials with an 180° SPS design or no SPS demands. The discriminatory power of the task was similar in the human and animal experiments. The findings demonstrate comparable SPS deficits in the early stages of AD in both humans and rodent models, which are not attributable to general memory impairment. SPS testing enables direct comparisons to be made between the cognitive performance of rats and humans, making it a promising approach for translational AD research.

The online version contains supplementary material available at 10.1038/s41598-026-36266-y.

## Linked entities

- **Diseases:** Alzheimer’s disease (MONDO:0004975)
- **Species:** Homo sapiens (taxon 9606), Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** memory impairment (MESH:D008569), AD (MESH:D000544), cognitive impairment (MESH:D003072)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12902105/full.md

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Source: https://tomesphere.com/paper/PMC12902105