Cited by 16Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsFunctional Brain Connectivity Studies

A review of neuroimaging-based data-driven approach for Alzheimer’s disease heterogeneity analysis

Liu, Lingyu, Sun, Shen, Kang, Wenjie, Wu, Shuicai, Lin, Lan·2024·Reviews in the Neurosciences

Abstract

Alzheimer's disease (AD) is a complex form of dementia and due to its high phenotypic variability, its diagnosis and monitoring can be quite challenging. Biomarkers play a crucial role in AD diagnosis and monitoring, but interpreting these biomarkers can be problematic due to their spatial and temporal heterogeneity. Therefore, researchers are increasingly turning to imaging-based biomarkers that employ data-driven computational approaches to examine the heterogeneity of AD. In this comprehensive review article, we aim to provide health professionals with a comprehensive view of past applications of data-driven computational approaches in studying AD heterogeneity and planning future research directions. We first define and offer basic insights into different categories of heterogeneity analysis, including spatial heterogeneity, temporal heterogeneity, and spatial-temporal heterogeneity. Then, we scrutinize 22 articles relating to spatial heterogeneity, 14 articles relating to temporal heterogeneity, and five articles relating to spatial-temporal heterogeneity, highlighting the strengths and limitations of these strategies. Furthermore, we discuss the importance of understanding spatial heterogeneity in AD subtypes and their clinical manifestations, biomarkers for abnormal orderings and AD stages, the recent advancements in spatial-temporal heterogeneity analysis for AD, and the emerging role of omics data integration in advancing personalized diagnosis and treatment for AD patients. By emphasizing the significance of understanding AD heterogeneity, we hope to stimulate further research in this field to facilitate the development of personalized interventions for AD patients.

Integrity signals

Registry

Crossref · 10.1515/revneuro-2023-0033

Cites

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Increasing research recognizes etiological and clinical heterogeneity of AD as a hallmark of AD and related diseases (ADRDs), making diagnosis, treatment, and drug development/testing more difficult.

    “More and more research is recognizing the etiological and clinical heterogeneity of AD as a hallmark of AD and related diseases (ADRDs), which makes it more difficult to diagnose, treat, and develop and test new medications for AD.”
  • Cognitive, neurological, psychological, and functional deficits in AD are complicated and different due to interactions with environmental factors.

    “Cognitive, neurological, psychological, and functional deficits are complicated and different as a result of these interactions with environmental factors.”
  • The interplay between phenotypes and genotypes is part of the heterogeneity of AD.

    “The interplay between phenotypes and genotypes is part of the heterogeneity of AD.”

The citation lists haven’t been fetched yet

References 96 · Cited by 16

Authors
Liu, L., Sun, S., Kang, W., Wu, S., & Lin, L.
Affiliations
Beijing University of Technology (CN)
Corresponding author
Lin, Lan
Venue
Reviews in the Neurosciences
Published
2023-07-10
Volume
35
Issue
2
Pages
121-139
ISSN
  • 0334-1763 (ISSN-L)
  • 2191-0200
OpenAlex
W4383506410
Cited by
16
References
96
Citations by year
2026: 5 · 2025: 4 · 2024: 6 · 2023: 1
FWCI
0.73
Type
journal article
Language
en
Open access
closed
Locations
  • Reviews in the Neurosciences (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Natural Science Foundation of China (81971683)
  • Natural Science Foundation of Beijing Municipality (L182010)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
Keywords
Alzheimer's disease, disease heterogeneity, spatial heterogeneity, temporal heterogeneity, spatiotemporal heterogeneity, imaging biomarkers, Alzheimer's disease subtypes, disease staging, multi-omics integration, personalized diagnosis, personalized treatment
MeSH terms
Alzheimer Disease, Brain, Humans, Biomarkers, Neuroimaging

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review