Evidence map›Paper›PMID 41346442›Full record

ArticleFrontiers in aging neuroscience2025

MRI-derived global small vessel disease burden serves as a marker of hippocampal sclerosis and clinical stage across the probable Alzheimer's disease continuum.

Ya-Che Chen, Ting-Bin Chen, Hsin-Chieh Chen

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2025. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Ya-Che ChenDepartment of Radiology, Tri-Service General Hospital, National Defense Medical University, Taipei, Taiwan.
Ting-Bin ChenDepartment of Neurology, Kuang Tien General Hospital, Taichung, Taiwan.
Hsin-Chieh ChenDepartment of Medical Equipment Development and Application, Hungkuang University, Taichung, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Cerebral small vessel disease (SVD) contributes to cognitive decline and hippocampal sclerosis (HS), yet its role across the Alzheimer's disease (AD) continuum remains incompletely understood. We aimed to determine whether composite MRI-based SVD scores serve as markers of cognitive impairment and HS in cognitively unimpaired (CU) individuals, patients with mild cognitive impairment (MCI), and those with probable AD dementia. Methods: We retrospectively analyzed 200 participants (24 CUs, 34 MCI, 142 AD) from the dementia registry at Kuang Tien General Hospital (January 2024-June 2025). SVD burden was quantified using three composite imaging scores: global SVD, cerebral amyloid angiopathy (CAA)-SVD, and hypertensive arteriopathy (HA)-SVD. Associations with cognitive performance, clinical staging, and HS were examined using multivariable regression models. Results: Global SVD and CAA-SVD scores correlated with Cognitive Abilities Screening Instrument (CASI) total and domain subscores, Clinical Dementia Rating (CDR) global score, and CDR sum of boxes (CDR-SB). Notably, only the global SVD score remained independently associated with both CDR-SB and HS after adjustment for relevant confounders. Discussion: MRI-derived global SVD burden, reflecting the combined effects of CAA and HA, is strongly associated with cognition, clinical staging, and HS across the probable AD continuum, supporting the global SVD score as a clinically useful biomarker of vascular contributions. Since MCI/AD diagnoses were based on clinical criteria without confirmation using cerebrospinal fluid or positive positron emission tomography biomarkers, potential misclassification may exist; findings should be interpreted with caution.

Indexed as

amyloid angiopathybiomarkerhypertensive arteriopathylacunemicrobleedwhite matter hyperintensity

Identifiers

PMID41346442
PMCPMC12672439

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