Evidence map›Paper›PMID 40851076›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2025

Alterations in MRI-visible perivascular spaces precede dementia diagnosis by 18 years in autosomal dominant Alzheimer's disease.

Riccardo Leone, Xenia Kobeleva, Bryan Rowe, Jeiran Choupan, John M Ringman, Giuseppe Barisano

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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.

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

5 citing papers in PubMed.

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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

6 authors.

Riccardo LeoneComputational Neurology Group, Ruhr University Bochum, Bochum, Germany.ORCID 0000-0001-5569-6090
Xenia KobelevaComputational Neurology Group, Ruhr University Bochum, Bochum, Germany.
Bryan RoweDepartment of Neurology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Jeiran ChoupanLaboratory of Neuro Imaging (LONI), Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
John M RingmanDepartment of Neurology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Giuseppe BarisanoDepartment of Neurosurgery, Stanford University, Stanford, California, USA.ORCID 0000-0001-5598-1369

Funding

Imaging CoreU19AG032438 · NIA · WASHINGTON UNIVERSITY · PI BATEMAN, RANDALL J · 2010 to 2025
$53.9M
USCADRC Diversity Supplement PachicanoP30AG066530 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LON S SCHNEIDER · 2020 to 2026
$27.8M
Motor, Visual, and Olfactory Changes in Genetic Subtypes of Alzheimer’s DiseaseR01AG062007 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI RINGMAN, JOHN M · 2019 to 2023
$4.1M
Structural and diffusion changes of perivascular space in aging, cognitive decline and Alzheimer's diseaseR01AG070825 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHOUPAN, JEIRAN · 2021 to 2025
$4.1M
Large-scale harmonization and integration of multi-modal ADNI data for the early detection of Alzheimer's disease and related dementiasR01NS128486 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Jeiran Choupan, Nasim Sheikh-Bahaei · 2022 to 2026
$4.0M
The structural and functional connectome across Alzheimer's disease subtypesU01AG051218 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI RINGMAN, JOHN M · 2015 to 2018
$3.6M
Mapping human brain perivascular space in lifespan using human connectome project dataRF1MH123223 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHOUPAN, JEIRAN · 2020 to 2020
$1.3M
FMRI in Pre-Symptomatic PS1-related Alzheimer's DiseaseK08AG022228 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RINGMAN, JOHN M · 2003 to 2005
$481k
Alzheimer's Association SG-20-690363-DIANAlzheimer's Drug Discovery Foundation RC-202405-2026586German Center for Neurodegenerative Diseases (DZNE)Helene and Lou Galen ProfessorshipJapan Agency for Medical Research and Development (AMED)Korea Dementia Research Center (KDRC)Korea Health Industry Development Institute (KHIDI)Ministry of Health & Welfare and Ministry of Science ICT, Republic of Korea RS-2024-00344521NIA NIH HHS K01AG22228NIA NIH HHS K08 AG022228NIA NIH HHS P30 AG066530NIA NIH HHS P30AG066530NIA NIH HHS R01 AG062007NIA NIH HHS R01AG062007NIA NIH HHS R01 AG070825NIA NIH HHS R01AG070825NIA NIH HHS U01 AG051218NIA NIH HHS U01AG051218NIA NIH HHS U19 AG032438NIA NIH HHS U19AG032438NIMH NIH HHS RF1 MH123223NIMH NIH HHS RF1MH123223NINDS NIH HHS R01 NS128486NINDS NIH HHS R01NS128486Raul Carrea Institute for Neurological Research (FLENI)Spanish Institute of Health Carlos III (ISCIII)
6 · The paper itself

Abstract

introductionPerivascular space (PVS) alterations are traditionally linked to cardiovascular risk factors and aging, but may also play a direct role in Alzheimer's disease (AD). To reduce confounding from age-related comorbidities, we examined PVSs in autosomal dominant AD (ADAD).

methodsIn this cross-sectional study of 96 non-demented individuals (62 mutation carriers), we quantified PVS count fraction and mean diameter in white matter and basal ganglia using automated magnetic resonance imaging analysis. Linear mixed models assessed group differences along the disease course, adjusting for cardiovascular risk factors.

resultsCompared to non-carriers, mutation carriers showed lower PVS count fraction in white matter and basal ganglia, and larger PVS diameter in basal ganglia and the temporal lobe. Changes were evident up to 18 years before expected dementia onset and followed trajectories similar to amyloid beta 42 and tau biomarkers. DISCUSSION: ADAD is associated with early PVS alterations, suggesting perivascular changes may be integral to primary AD pathology. HIGHLIGHTS: Autosomal dominant Alzheimer's disease (ADAD) mutation carriers have reduced magnetic resonance imaging-visible perivascular space (PVS) count fraction in the white matter and basal ganglia. ADAD mutation carriers show enlarged PVS in the basal ganglia and temporal white matter. PVS alterations start 18 years before the estimated time of dementia diagnosis. The spatial localization of PVS changes overlaps with regions of amyloid beta (Aβ) accumulation. The temporal evolution of PVS alterations aligns with Aβ and tau changes in the cerebrospinal fluid.

Indexed as

Alzheimer DiseaseBasal GangliaGlymphatic SystemWhite MatterAgedAmyloid beta-PeptidesCross-Sectional StudiesDisease ProgressionFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedMutationtau ProteinsAmyloid beta-Peptidestau ProteinsAlzheimer's diseaseautosomal dominant Alzheimer's diseasecerebral small vessel diseasedominantly inherited Alzheimer's diseasemagnetic resonance imagingperivascular spaces

Identifiers

PMID40851076
PMCPMC12375433

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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.