Evidence map›Paper›PMID 41200502›Full record

ArticleJournal of Alzheimer's disease reports

Comparative analysis of PET and multiparametric MRI biomarkers in Alzheimer's disease continuum cohort.

Chileka Chiyanika, Nga Yan Chan, Wanting Liu, Lisa Wing Chi Au, Weitian Chen, Chunlei Liu, Sirong Chen, Eric Yim Lung Leung, Chi Lai Ho, Yuan Cai and 5 more

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease reports. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

15 authors.

Chileka ChiyanikaDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, China.ORCID https://orcid.org/0000-0002-4744-1714
Nga Yan ChanDepartment of Imaging and Interventional Radiology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Wanting LiuGerald Choa Neuroscience Institute, Lui Che Woo Institute of Innovative Medicine, Lau Tat-Chuen Research Centre of Brain Degenerative Diseases Chinese, Division of Neurology, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Lisa Wing Chi AuGerald Choa Neuroscience Institute, Lui Che Woo Institute of Innovative Medicine, Lau Tat-Chuen Research Centre of Brain Degenerative Diseases Chinese, Division of Neurology, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Weitian ChenDepartment of Imaging and Interventional Radiology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Chunlei LiuDepartment of Electrical Engineering and Computer Sciences, University of California, Berkeley, CA, USA.
Sirong ChenDepartment of Nuclear Medicine & PET, Hong Kong Sanatorium & Hospital, Hong Kong, China.
Eric Yim Lung LeungDepartment of Nuclear Medicine & PET, Hong Kong Sanatorium & Hospital, Hong Kong, China.
Chi Lai HoDepartment of Nuclear Medicine & PET, Hong Kong Sanatorium & Hospital, Hong Kong, China.
Yuan CaiGerald Choa Neuroscience Institute, Lui Che Woo Institute of Innovative Medicine, Lau Tat-Chuen Research Centre of Brain Degenerative Diseases Chinese, Division of Neurology, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Ho KoGerald Choa Neuroscience Institute, Lui Che Woo Institute of Innovative Medicine, Lau Tat-Chuen Research Centre of Brain Degenerative Diseases Chinese, Division of Neurology, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Qianyun ChenDepartment of Imaging and Interventional Radiology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Winnie ChuDepartment of Imaging and Interventional Radiology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Vincent Chung Tong MokGerald Choa Neuroscience Institute, Lui Che Woo Institute of Innovative Medicine, Lau Tat-Chuen Research Centre of Brain Degenerative Diseases Chinese, Division of Neurology, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
Jill AbrigoDepartment of Imaging and Interventional Radiology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Non-invasive biomarkers are key to early Alzheimer's disease (AD) detection. Multiparametric MRI and advanced imaging offer promising, accessible tools for identifying AD-related changes, supporting timely diagnosis and intervention. Objective: To assess how accurately multiparametric MRI biomarkers identify AD using Aβ-PET imaging as the reference, and to evaluate whether MRI metrics in AD-related brain regions can distinguish between Aβ-positive and Aβ-negative subjects across the AD continuum. Methods: In this exploratory retrospective study, 44 subjects aged 50-80 years were classified based on their PET and MRI biomarkers following the NIA-AA 2024 framework. MRI metrics included selected regional brain volumes (T1-weighted), mean diffusivity and fractional anisotropy (DTI-MD, DTI-FA), quantitative susceptibility mapping (QSM), and T1rho imaging. These were compared with amyloid load, and diagnostic performance was assessed using area-under-the-curve (AUC) analysis. Results: 25 subjects were Aβ+ (AD continuum), while 19 were Aβ- (controls). Volumes of the hippocampus, thalamus, amygdala, cingulate, putamen, and corpus callosum and DTI-MD in the hippocampus, corpus callosum, cuneus, and cingulate showed optimal diagnostic performance (AUC ≥ 0.80), with hippocampal volume and hippocampal DTI-MD showing AUCs > 0.90, (both p < 0.05). Combining hippocampal volumetry and hippocampal DTI-MD (AUC = 0.95, p < 0.001) improved diagnostic accuracy by 2.1% compared to using either biomarker alone. LASSO logistic regression analysis showed that amyloid positivity was significantly associated with hippocampal volume (p < 0.001). Conclusions: Hippocampal volumetry and hippocampal DTI-MD may be superior and more sensitive imaging biomarkers for AD. Their combined use could improve diagnostic accuracy and enhance early AD detection.

Indexed as

Alzheimer's diseasediffusion tensor imaging-fractional anisotropydiffusion tensor imaging-mean diffusivityquantitative susceptibility mappingT1rho

Identifiers

PMID41200502
PMCPMC12586874

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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.