Evidence map›Paper›PMID 41656106›Full record

ArticleMagnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine2026

White Matter Microstructural Alterations Mediate the Association between Polygenic Risk for Alzheimer's Disease and Cognitive Performance in Clinically Asymptomatic Adults.

Rui Zou, Kaito Takabayashi, Christina Andica, Wataru Uchida, Takafumi Kitagawa, Koyo Mizuta, Akifumi Hagiwara, Junko Kikuta, Shigeki Aoki, Koji Kamagata

Abstract read
In one paragraph

Article in Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine, 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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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

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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

10 authors.

Rui ZouDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Kaito TakabayashiDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Christina AndicaDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Wataru UchidaDepartment of Data Science, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Takafumi KitagawaDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Koyo MizutaDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Akifumi HagiwaraDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Junko KikutaDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Shigeki AokiDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Koji KamagataDepartment of Radiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAlzheimer's disease (AD) is a progressive neurodegenerative disorder influenced by genetic factors, with a long preclinical phase characterized by subtle alterations in brain microstructure. Although the apolipoprotein E ε4 allele is a well-established genetic risk factor, AD is increasingly recognized as a polygenic condition. However, how polygenic risk manifests in white matter (WM) microstructure and cognition remains unclear. This study aims to investigate the associations between AD polygenic risk scores (ADPRS), WM microstructure, and cognitive performance in clinically asymptomatic adults.

methodsData from 36400 individuals (aged 45-83 years) in the UK Biobank were analyzed. Diffusion tensor imaging and neurite orientation dispersion and density imaging metrics were extracted from 48 WM tracts. General linear models were used to examine associations between ADPRS, WM integrity, and 10 cognitive measures. Mediation analyses were conducted to test whether WM microstructure mediated the relationship between ADPRS and cognitive performance.

resultsHigher ADPRS was significantly associated with reduced fractional anisotropy and intracellular volume fraction, and with increased mean, axial, and radial diffusivity, as well as isotropic volume fraction across limbic and association fibers, particularly in the cingulum hippocampus, fornix, posterior thalamic radiation, and superior fronto-occipital fasciculus. Higher ADPRS was also associated with poorer cognitive performance, most prominently on tests of executive function (Trail Making Test B), episodic memory (Paired Associate Learning), and processing speed (Symbol Digit Substitution). Mediation analysis revealed that WM microstructural alterations, especially increased radial diffusivity and reduced fractional anisotropy in the posterior thalamic radiation, partially mediated the association between ADPRS and cognitive performance, accounting for up to 4.88% of the total effect.

conclusionADPRS is linked to selective WM microstructural alterations and subtle cognitive difference in clinically asymptomatic adults. WM microstructural changes partially mediate the association between ADPRS and cognitive performance.

Indexed as

Alzheimer DiseaseCognitionDiffusion Tensor ImagingWhite MatterAgedAged, 80 and overFemaleGenetic Risk ScoreHumansMaleMiddle AgedRisk Factorscognitive functionneurite orientation dispersion and density imagingpolygenic risk score of Alzheimer’s diseaseUK Biobankwhite matter microstructure

Identifiers

PMID41656106
PMCPMC13481157

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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.