Evidence map›Paper›PMID 39001624›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2024

Assessing cognitive impairment and disability in older adults through the lens of whole brain white matter patterns.

Hyun Woong Roh, Nishant Chauhan, Sang Won Seo, Seong Hye Choi, Eun-Joo Kim, Soo Hyun Cho, Byeong C Kim, Jin Wook Choi, Young-Sil An, Bumhee Park and 7 more

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. 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

17 authors.

Hyun Woong RohDepartment of Psychiatry, Ajou University School of Medicine, Suwon, Republic of Korea.
Nishant ChauhanCognitive Science Research Group, Korea Brain Research Institute, Daegu, Republic of Korea.
Sang Won SeoDepartment of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Seong Hye ChoiDepartment of Neurology, Inha University School of Medicine, Incheon, Republic of Korea.
Eun-Joo KimDepartment of Neurology, Pusan National University Hospital, Pusan National University School of Medicine and Medical Research Institute, Busan, Republic of Korea.
Soo Hyun ChoDepartment of Neurology, Chonnam National University Medical School, Chonnam National University Hospital, Gwangju, Republic of Korea.
Byeong C KimDepartment of Neurology, Chonnam National University Medical School, Chonnam National University Hospital, Gwangju, Republic of Korea.
Jin Wook ChoiDepartment of Radiology, Ajou University School of Medicine, Suwon, Republic of Korea.
Young-Sil AnDepartment of Nuclear Medicine and Molecular Imaging, Ajou University School of Medicine, Suwon, Republic of Korea.
Bumhee ParkDepartment of Biomedical Informatics, Ajou University School of Medicine, Suwon, Republic of Korea.
Sun Min LeeDepartment of Neurology, Ajou University School of Medicine, Suwon, Republic of Korea.
So Young MoonDepartment of Neurology, Ajou University School of Medicine, Suwon, Republic of Korea.
You Jin NamDepartment of Psychiatry, Ajou University School of Medicine, Suwon, Republic of Korea.
Sunhwa HongDepartment of Psychiatry, Ajou University School of Medicine, Suwon, Republic of Korea.
Sang Joon SonDepartment of Psychiatry, Ajou University School of Medicine, Suwon, Republic of Korea.
Chang Hyung HongDepartment of Psychiatry, Ajou University School of Medicine, Suwon, Republic of Korea.
Dongha LeeCognitive Science Research Group, Korea Brain Research Institute, Daegu, Republic of Korea.ORCID 0000-0001-8316-2141

Funding

Korea Brain Research Institute 24-BR-05-01Korea Brain Research Institute 24-BR-05-02Korea Health Industry Development Institute, Ministry of Health and Welfare HI22C0724Korea Health Industry Development Institute, Ministry of Health and Welfare HR21C1003Korea Health Industry Development Institute, Ministry of Health and Welfare HR22C1734Korea Health Industry Development Institute, Ministry of Health and Welfare HV22C0073Korea Health Industry Development Institute, Ministry of Health and Welfare HV22C0164National Research Foundation of Korea, Ministry of Science and ICT NRF-2019R1A5A2026045
6 · The paper itself

Abstract

introductionThis study aimed to explore the potential of whole brain white matter patterns as novel neuroimaging biomarkers for assessing cognitive impairment and disability in older adults.

methodsWe conducted an in-depth analysis of magnetic resonance imaging (MRI) and amyloid positron emission tomography (PET) scans in 454 participants, focusing on white matter patterns and white matter inter-subject variability (WM-ISV).

resultsThe white matter pattern ensemble model, combining MRI and amyloid PET, demonstrated a significantly higher classification performance for cognitive impairment and disability. Participants with Alzheimer's disease (AD) exhibited higher WM-ISV than participants with subjective cognitive decline, mild cognitive impairment, and vascular dementia. Furthermore, WM-ISV correlated significantly with blood-based biomarkers (such as glial fibrillary acidic protein and phosphorylated tau-217 [p-tau217]), and cognitive function and disability scores. DISCUSSION: Our results suggest that white matter pattern analysis has significant potential as an adjunct neuroimaging biomarker for clinical decision-making and determining cognitive impairment and disability. HIGHLIGHTS: The ensemble model combined both magnetic resonance imaging (MRI) and amyloid positron emission tomography (PET) and demonstrated a significantly higher classification performance for cognitive impairment and disability. Alzheimer's disease (AD) revealed a notably higher heterogeneity compared to that in subjective cognitive decline, mild cognitive impairment, or vascular dementia. White matter inter-subject variability (WM-ISV) was significantly correlated with blood-based biomarkers (glial fibrillary acidic protein and phosphorylated tau-217 [p-tau217]) and with the polygenic risk score for AD. White matter pattern analysis has significant potential as an adjunct neuroimaging biomarker for clinical decision-making processes and determining cognitive impairment and disability.

Indexed as

BiomarkersBrainCognitive DysfunctionMagnetic Resonance ImagingPositron-Emission TomographyWhite MatterAgedAged, 80 and overAlzheimer DiseaseFemaleHumansMaleNeuroimagingtau ProteinsBiomarkerstau Proteinscognitive impairmentfunctional disabilityMRI and PET imagingneurodegenerationwhite matter pattern

Identifiers

PMID39001624
PMCPMC11497644

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LicenceCC BY-NC-ND
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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.