Evidence map›Paper›PMID 38802684›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2024

Interactions between physical exercise, associative memory, and genetic risk for Alzheimer's disease.

Kinga Igloi, Blanca Marin Bosch, Noémie Kuenzi, Aurélien Thomas, Estelle Lauer, Aurélien Bringard, Sophie Schwartz

Abstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

7 authors.

Kinga IgloiDepartment of Fundamental Neurosciences, University of Geneva, CH-1211 Geneva, Switzerland.ORCID 0000-0002-3428-8474
Blanca Marin BoschDepartment of Fundamental Neurosciences, University of Geneva, CH-1211 Geneva, Switzerland.
Noémie KuenziDepartment of Fundamental Neurosciences, University of Geneva, CH-1211 Geneva, Switzerland.
Aurélien ThomasFaculty Unit of Toxicology, CURML, Faculty of Biology and Medicine, University of Lausanne, CH-1015 Lausanne, Switzerland.
Estelle LauerUnit of Forensic Toxicology and Chemistry, CURML, Lausanne and Geneva University Hospitals, Lausanne, CH-1011 Geneva, Switzerland.
Aurélien BringardDepartment of Pneumology, Geneva University Hospitals, CH-1011 Geneva, Switzerland.
Sophie SchwartzDepartment of Fundamental Neurosciences, University of Geneva, CH-1211 Geneva, Switzerland.

Funding

Swiss National Science Foundation P1GEP3_184161Swiss National Science Foundation SNF 320030-182589
6 · The paper itself

Abstract

The ε4 allele of the APOE gene heightens the risk of late onset Alzheimer's disease. ε4 carriers, may exhibit cognitive and neural changes early on. Given the known memory-enhancing effects of physical exercise, particularly through hippocampal plasticity via endocannabinoid signaling, here we aimed to test whether a single session of physical exercise may benefit memory and underlying neurophysiological processes in young ε3 carriers (ε3/ε4 heterozygotes, risk group) compared with a matched control group (homozygotes for ε3). Participants underwent fMRI while learning picture sequences, followed by cycling or rest before a memory test. Blood samples measured endocannabinoid levels. At the behavioral level, the risk group exhibited poorer associative memory performance, regardless of the exercising condition. At the brain level, the risk group showed increased medial temporal lobe activity during memory retrieval irrespective of exercise (suggesting neural compensatory effects even at baseline), whereas, in the control group, such increase was only detectable after physical exercise. Critically, an exercise-related endocannabinoid increase correlated with task-related hippocampal activation in the control group only. In conclusion, healthy young individuals carrying the ε4 allele may present suboptimal associative memory performance (when compared with homozygote ε3 carriers), together with reduced plasticity (and functional over-compensation) within medial temporal structures.

Indexed as

Alzheimer DiseaseExerciseMagnetic Resonance ImagingAdultApolipoprotein E4Association LearningBrainEndocannabinoidsFemaleGenetic Predisposition to DiseaseHeterozygoteHippocampusHumansMaleMemoryYoung AdultApolipoprotein E4EndocannabinoidsAlzheimer’s diseaseendocannabinoidsfMRImemoryphysical exercise

Identifiers

PMID38802684
PMCPMC11129939

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.