Evidence map›Paper›PMID 41065118›Full record

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

Retinal microvascular alterations in Alzheimer's disease: Linking blood plasma biomarkers and cerebral small vessel pathology.

William Robert Kwapong, Ning Wu, Weihong Lin, Jianing Shen, Youjie Wang, Jiajing Qian, Caiyun Wen, Xiaoqian Luan, Yuntao Liu, Haoran Cheng and 7 more

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Mendelian randomization evidence refines retinal alterations in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
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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

17 authors.

William Robert KwapongDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Ning WuDepartment of Medical Imaging, Yanjing Medical College, Capital Medical University, Beijing, China.
Weihong LinKey Laboratory of Alzheimer's Disease of Zhejiang Province, Wenzhou, China.
Jianing ShenDepartment of Geriatrics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Youjie WangDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, China.
Jiajing QianDepartment of Geriatrics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Caiyun WenDepartment of Geriatrics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Xiaoqian LuanDepartment of Geriatrics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Yuntao LiuDepartment of Geriatrics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Haoran ChengDepartment of Geriatrics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Huihua QiuDepartment of Geriatrics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Carol Y CheungDepartment of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Chunwen ZhengDepartment of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Yinhe LiuOphthalmology Department, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Yunjun YangDepartment of Radiology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Vincent MokDepartment of Medicine and Therapeutics, Division of Neurology, Margaret K.L. Cheung Research Centre for Management of Parkinsonism, Lui Che Woo Institute of Innovative Medicine, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Zhen WangKey Laboratory of Alzheimer's Disease of Zhejiang Province, Wenzhou, China.

Funding

Key Laboratory of Novel Nuclide Technologies on Precision DiagnosisTreatment & Clinical Transformation of Wenzhou City 2023HZSY0012Zhejiang Clinovation Pride Code CXTD202501044
6 · The paper itself

Abstract

backgroundRetinal microvascular alterations, detectable via color fundus photography (CFP), may reflect cerebral microvascular pathology in Alzheimer's disease (AD). However, their associations with blood-based biomarkers and cerebral small vessel disease (SVD) remain unclear.

methodsThis cross-sectional study included 72 AD patients and 82 cognitively unimpaired (CU) controls. Participants underwent CFP, plasma biomarker analysis (amyloid beta [Aβ]42, Aβ42/40, phosphorylated tau [p-tau]181, p-tau217), and 3T magnetic resonance imaging. Retinal microvascular metrics (vessel density [VD], fractal dimension [FD]) were analyzed alongside SVD markers (white matter hyperintensities [WMHs], SVD burden) and medial temporal lobe atrophy (MTA).

resultsAD patients exhibited significantly reduced VD and FD compared to CU (all p < 0.001), with strong diagnostic accuracy (area under the curve: 0.969 for VD; 0.904 for FD). Retinal microvascular impairment correlated with plasma biomarkers (lower Aβ42, Aβ42/40; elevated p-tau181, p-tau217; all p < 0.05) and neuroimaging markers of SVD (WMHs, MTA; all p < 0.05). Apolipoprotein E ε4 carriers showed more severe retinal microvascular damage (p < 0.001). DISCUSSION: Retinal microvascular alterations, assayed via CFP, are linked to AD-specific proteinopathy and cerebrovascular pathology, supporting CFP as a scalable, non-invasive tool for AD biomarker discovery. HIGHLIGHTS: Retinal microvasculature assayed via color fundus photography (CFP) is sensitive to microvascular damage and can differentiate Alzheimer's disease (AD) from cognitively unimpaired controls. Retinal microvascular damage in AD is associated with phosphorylated tau [p-tau]181, p-tau217, p-tau217/amyloid beta (Aβ)42, and increased amyloid burden (lower Aβ42 and Aβ42/40). Retinal microvascular damage in AD is associated with increased cerebral small vessel burden.

Indexed as

Alzheimer DiseaseCerebral Small Vessel DiseasesMicrovesselsRetinal VesselsAgedAmyloid beta-PeptidesBiomarkersCross-Sectional StudiesFemaleHumansMagnetic Resonance ImagingMaleMiddle Agedtau ProteinsAmyloid beta-PeptidesBiomarkerstau Proteinsamyloidcerebral small vessel diseaseretinal microvasculaturetau

Identifiers

PMID41065118
PMCPMC12509039

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Registered trials

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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.