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Multi-modal latent factor exploration of atrophy, cognitive and tau heterogeneity in Alzheimer's disease
Sun N, Mormino EC, Chen J, Sabuncu MR, Yeo BTT, Alzheimer’s Disease Neuroimaging Initiative.. NeuroImage, 2019-07-22
Topic: Amyloid, tau and blood-test diagnosis
Individuals with Alzheimer's disease (AD) dementia exhibit significant heterogeneity across clinical symptoms, atrophy patterns, and spatial distribution of Tau deposition. Most previous studies of AD heterogeneity have focused on atypical clinical subtypes, defined subtypes with a single modality, or restricted their analyses to a priori brain regions and cognitive tests. Here, we considered a data-driven hierarchical Bayesian model to identify latent factors from atrophy patterns and cognitive deficits simultaneously, thus exploiting the rich dimensionality within each modality.
Cite this study APA, Vancouver, BibTeX · download .bib or .ris
APA 7th
Sun, N., Mormino, E. C., Chen, J., Sabuncu, M. R., Yeo, B. T. T., & Alzheimer’s Disease Neuroimaging Initiative. (2019). Multi-modal latent factor exploration of atrophy, cognitive and tau heterogeneity in Alzheimer's disease. NeuroImage. https://doi.org/10.1016/j.neuroimage.2019.116043
Vancouver
Sun N, Mormino EC, Chen J, Sabuncu MR, Yeo BTT, Alzheimer’s Disease Neuroimaging Initiative. Multi-modal latent factor exploration of atrophy, cognitive and tau heterogeneity in Alzheimer's disease. NeuroImage. 2019. doi:10.1016/j.neuroimage.2019.116043. PMID: 31344486.
BibTeX
@article{sun2019-31344486,
author = {Sun, N. and Mormino, E. C. and Chen, J. and Sabuncu, M. R. and Yeo, B. T. T. and {Alzheimer’s Disease Neuroimaging Initiative}},
title = {{Multi-modal latent factor exploration of atrophy, cognitive and tau heterogeneity in Alzheimer's disease}},
journal = {NeuroImage},
year = {2019},
doi = {10.1016/j.neuroimage.2019.116043},
pmid = {31344486},
url = {https://doi.org/10.1016/j.neuroimage.2019.116043}
}
Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. Check the citation against the original before you use it.
Key findings
- Most previous studies of AD heterogeneity have focused on atypical clinical subtypes, defined subtypes with a single modality, or restricted their analyses to a priori brain regions and cognitive tests.
- Here, we considered a data-driven hierarchical Bayesian model to identify latent factors from atrophy patterns and cognitive deficits simultaneously, thus exploiting the rich dimensionality within each modality.
- Unlike most previous studies, our model allows each factor to be expressed to varying degrees within an individual, in order to reflect potential multiple co-existing pathologies.
- By applying our model to ADNI-GO/2 AD dementia participants, we found three atrophy-cognitive factors.
Why it matters
This study used a data-driven model to identify latent factors from atrophy patterns and cognitive deficits in people with Alzheimer's disease dementia. It is an observational study of disease heterogeneity, so it does not treat, cure, or prevent Alzheimer's disease.
Study details
- Study designlongitudinal study
- Evidence strengthModerate
How this study scored 54/100
Published in a peer-reviewed journal, and it is a longitudinal study following the same people over time. Scored zero for sample size, effect reported, studied in people and randomised / blinded because the record does not state it.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (NeuroImage) |
| Journal's citation record | 4 / 4 | NeuroImage: journal h-index 523 (OpenAlex, 2026-10-29) |
| Study design | 7 / 12 | A longitudinal study following the same people over time |
| Strength of evidence | 3 / 5 | Rated “moderate” in our summary |
| Peer-review validation | 10 / 10 | Peer-reviewed. Published as an article in a named peer-reviewed journal. |
| How recent | 2 / 5 | 2019 — within 10 year(s) of the newest study here |
| Sample size | 0 / 4 | Participant count not stated — scores zero (not stated in the record — scored 0) |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 0 / 3 | Not stated whether this was studied in people — scores zero (not stated in the record — scored 0) |
| Randomised / blinded | 0 / 2 | No randomisation or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 4 / 7 | Cited 47 times (OpenAlex, 2026-10-10) |
| Citations per year | 2 / 5 | 5.2 citations a year over 9 year(s) since 2019 |
| Impact for its field and year | 3 / 6 | Cited 5.4× the average for papers of its field and year (OpenAlex FWCI) |
| Cited by studies here | 1 / 6 | Cited by 1 other studies in this library |
| Still being cited | 1 / 4 | Cited 11 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | 3 / 4 | Last-listed author B.T. Thomas Yeo: h-index 77 (OpenAlex, whole career) |
| Institution's track record | 3 / 3 | Stanford University: institution h-index 2,684 (OpenAlex) |
| Multi-centre collaboration | 2 / 3 | OpenAlex lists 7 institution(s) in 2 countries |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 31344486) |
| Free to read | 0 / 2 | Behind a paywall — scores zero |
| Total | 54 / 100 | — |
What each of these 20 components measures, and what this score is not →
Read the original
- DOI: 10.1016/j.neuroimage.2019.116043
- PubMed: 31344486
- Original source →
- Free full text: NeuroImage →
Full text: free to read — OpenAlex lists this copy as free to read: the link above (checked 6 Feb 1020).
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