A review of neuroimaging-based data-driven approach for Alzheimer’s disease heterogeneity analysis
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.
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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.”
From Recent Advances in Therapeutics for the Treatment of Alzheimer’s Disease (2024) · cites this paper as [191]
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.”
From Recent Advances in Therapeutics for the Treatment of Alzheimer’s Disease (2024) · cites this paper as [191]
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.”
From Recent Advances in Therapeutics for the Treatment of Alzheimer’s Disease (2024) · cites this paper as [191]
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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
- Publisher
- Walter de Gruyter GmbH
- 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
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