Evidence map›Paper›PMID 41775699›Full record

ArticleTranslational psychiatry2026

Stage-Dependent mediation of white matter hyperintensities between plasma biomarkers and cognitive function in Alzheimer's disease.

Hui Juan Chen, Yihao Guo, Weiyuan Huang, Kun Zhang, Tao Liu, Feng Chen

Abstract read
In one paragraph

Article in Translational psychiatry, 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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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hui Juan ChenDepartment of Radiology, Hainan General Hospital, and Hainan Affiliated Hospital of Hainan Medical University, Haikou, China.
Yihao GuoDepartment of Radiology, Hainan General Hospital, and Hainan Affiliated Hospital of Hainan Medical University, Haikou, China.
Weiyuan HuangDepartment of Radiology, Hainan General Hospital, and Hainan Affiliated Hospital of Hainan Medical University, Haikou, China.
Kun ZhangDepartment of Neurology, Hainan General Hospital, and Hainan Affiliated Hospital of Hainan Medical University, Haikou, China.
Tao LiuDepartment of Neurology, Hainan General Hospital, and Hainan Affiliated Hospital of Hainan Medical University, Haikou, China.
Feng ChenDepartment of Radiology, Hainan General Hospital, and Hainan Affiliated Hospital of Hainan Medical University, Haikou, China. fenger0802@hainmc.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

White matter hyperintensities (WMHs) are common in Alzheimer's disease (AD) and may contribute to cognitive impairment. However, the associations between regional WMH volumes, cognitive domains, and plasma biomarkers remain unclear. This study aimed to explore these relationships across the AD spectrum. A total of 311 participants were enrolled, including healthy controls (HC), individuals with subjective cognitive decline (SCD), mild cognitive impairment (MCI), and AD. All participants underwent comprehensive neuropsychological assessment, brain magnetic resonance imaging, and plasma biomarker analysis. WMH volumes were segmented using United Imaging software and classified based on anatomical location: juxtaventricular WMH (juxWMH), periventricular WMH (pWMH), juxtacortical WMH (jcWMH), and deep WMH (dWMH). Correlations among regional WMH volumes, plasma biomarkers, and cognitive domains were analyzed with multiple comparisons. Path analysis was used to assess potential mediation effects. Mediation analyses using bootstrapping were conducted separately in cognitively unimpaired and cognitively impaired groups to assess WMH-mediated pathways between biomarkers and cognition. Compared with HC, SCD, and MCI groups, the AD group showed significantly increased log-transformed (lg) juxWMH volumes (all P < 0.05, Bonferroni corrected). The AD group showed significantly larger lgpWMH and lgjcWMH volumes than HC, SCD and AD groups (all P < 0.05). Lower plasma Aβ42/Aβ40 ratio was associated with higher lgjuxWMH, lgpWMH, and lgjcWMH volumes. Higher lgjuxWMH volume was associated with worse memory (r = -0.16, P = 0.006), language (r = -0.34, P < 0.001), and executive function (r = 0.18, P = 0.003). Similar trends were found for lgpWMH and lgjcWMH volumes. Mediation analysis revealed that in cognitively unimpaired individuals, juxWMH and pWMH primarily mediated amyloid-cognitive associations, while in cognitively impaired patients, mediation expanded to include neuroinflammatory and neurodegeneration pathways across multiple location-specific WMH. Location-specific WMH demonstrate stage-dependent mediation patterns in AD pathophysiology, evolving from amyloid-driven changes to multi-factorial processes. These findings provide insights for developing targeted therapeutic strategies at different disease stages.

Indexed as

Alzheimer DiseaseCognitionCognitive DysfunctionWhite MatterAgedAmyloid beta-PeptidesBiomarkersBrainCase-Control StudiesFemaleHumansMagnetic Resonance ImagingMaleNeuropsychological TestsPeptide FragmentsAmyloid beta-PeptidesBiomarkersPeptide Fragments

Identifiers

PMID41775699
PMCPMC12982599

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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.