Evidence map›Paper›PMID 42374489›Full record

ArticleAlzheimer's research & therapy2026

Structural and molecular determinants of medial temporal lobe network vulnerability in aging and Alzheimer's disease.

Elise Saul, Léa Chauveau, Brigitte Landeau, Jade Lasserve, Blandine Montagne, Emilie Foyard, Géraldine Poisnel, Gaël Chételat, Robin de Flores, Medit-Ageing Research Group

Registry-linked trialAbstract read
In one paragraph

Article in Alzheimer's research & therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02977819 (Interventional Study in Cognitively Intact Seniors Aiming to Assess the Effects of Meditation Training and Foreign Language Learning on Behavioral, Biological and Neuroimaging Measures), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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.

NCT02977819 nacompletednot on this map

Interventional Study in Cognitively Intact Seniors Aiming to Assess the Effects of Meditation Training and Foreign Language Learning on Behavioral, Biological and Neuroimaging Measures

TypeinterventionalSponsorInstitut National de la Santé Et de la Recherche Médicale, FranceRan2016 to 2023Enrolled137ConditionsCognitive AgingArmsMeditation practice, Learning English as a foreign language
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

10 authors.

Elise SaulNormandie Univ, UNICAEN, INSERM, UA20, NEUROPRESAGE, GIP Cyceron, , Bd Henri Becquerel, BP 5229, Caen, 14074, cedex 5, France.
Léa ChauveauNormandie Univ, UNICAEN, INSERM, UA20, NEUROPRESAGE, GIP Cyceron, , Bd Henri Becquerel, BP 5229, Caen, 14074, cedex 5, France.
Brigitte LandeauNormandie Univ, UNICAEN, INSERM, UA20, NEUROPRESAGE, GIP Cyceron, , Bd Henri Becquerel, BP 5229, Caen, 14074, cedex 5, France.
Jade LasserveNormandie Univ, UNICAEN, INSERM, UA20, NEUROPRESAGE, GIP Cyceron, , Bd Henri Becquerel, BP 5229, Caen, 14074, cedex 5, France.
Blandine MontagneNormandie Univ, UNICAEN, INSERM, UA20, NEUROPRESAGE, GIP Cyceron, , Bd Henri Becquerel, BP 5229, Caen, 14074, cedex 5, France.
Emilie FoyardNormandie Univ, UNICAEN, INSERM, UA20, NEUROPRESAGE, GIP Cyceron, , Bd Henri Becquerel, BP 5229, Caen, 14074, cedex 5, France.
Géraldine PoisnelNormandie Univ, UNICAEN, INSERM, UA20, NEUROPRESAGE, GIP Cyceron, , Bd Henri Becquerel, BP 5229, Caen, 14074, cedex 5, France.
Gaël ChételatNormandie Univ, UNICAEN, INSERM, UA20, NEUROPRESAGE, GIP Cyceron, , Bd Henri Becquerel, BP 5229, Caen, 14074, cedex 5, France.
Robin de FloresNormandie Univ, UNICAEN, INSERM, UA20, NEUROPRESAGE, GIP Cyceron, , Bd Henri Becquerel, BP 5229, Caen, 14074, cedex 5, France. deflores@cyceron.fr.ORCID https://orcid.org/0000-0003-3953-3392
Medit-Ageing Research Group

Funding

European Union's Horizon 2020 Research and Innovation Program 667696
6 · The paper itself

Abstract

backgroundThe medial temporal lobe is organized into two memory-critical networks: the anterior-temporal and posterior-medial systems. While these systems show selective vulnerability to aging and Alzheimer's disease, the underlying structural and molecular determinants of this susceptibility remain unclear. We aimed to characterize the specific white matter pathways supporting these networks, investigate how amyloid-β and neuroinflammation interact to impact their integrity, and determine if structural changes relate to functional connectivity alterations.

methodsIn 88 cognitively unimpaired (CU) older adults (≥ 65 years) from the Age-Well cohort (NCT02977819), we combined longitudinal diffusion MRI tractography, resting-state fMRI, amyloid-β PET (Florbetapir), and plasma glial fibrillary acidic protein (GFAP). We reconstructed fiber pathways of the perirhinal (anterior-temporal system hub) and parahippocampal (posterior-medial system hub) cortices and quantified their microstructural integrity, network connectivity, and relationships to pathology.

resultsThe anterior-temporal and posterior-medial systems relied on partly distinct structural pathways. Both involved the inferior longitudinal and cingulum bundles, but the anterior-temporal system was specifically associated to their inferior portions, as well as thalamic radiations, and callosal fibers, whereas the posterior-medial system relied more on their superior portions and the inferior fronto-occipital fasciculus. We identified a non-linear, inverted U-shaped association between pathway integrity and amyloid-β burden, suggesting dynamic structural changes across early pathological stages. Crucially, plasma GFAP moderated this relationship for the posterior-medial pathway: the negative impact of amyloid-β on structural integrity was exacerbated in individuals with higher astroglial reactivity, highlighting a synergistic pathological effect. Finally, in high amyloid-β individuals, increased anterior-temporal functional connectivity correlated with lower anterior-temporal pathway integrity, suggesting that network higher FC may represent a maladaptive response to early amyloid-β deposition leading to white matter integrity loss.

conclusionsTogether, our findings reveal distinct mechanisms of vulnerability within medial temporal networks: while the posterior-medial system is primarily sensitive to the synergistic effects of amyloid-β and astroglial reactivity, the anterior-temporal system shows lower structural integrity linked to higher FC in the presence of amyloid. By providing a mechanistic framework for these early disruptions, this study advances the understanding of preclinical Alzheimer's disease and identifies specific structural-functional signatures that could serve as sensitive biomarkers for targeted interventions.

Indexed as

AgingAlzheimer DiseaseNerve NetTemporal LobeAgedAged, 80 and overAmyloid beta-PeptidesDiffusion Tensor ImagingFemaleGlial Fibrillary Acidic ProteinHumansLongitudinal StudiesMagnetic Resonance ImagingMaleNeural PathwaysPositron-Emission TomographyAmyloid beta-PeptidesGlial Fibrillary Acidic ProteinAgingAlzheimer’s DiseaseAmyloid-βFunctional connectivityMedial temporal lobeNeuroinflammationStructural connectivity

Identifiers

PMID42374489
PMCPMC13591752

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Registered trials

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.