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Enhanced diagnostic interpretation of the MoCA using machine learning
Christian Gourdeau, Charles L. Gourdeau, Patrick J. Bernier, Robert Jr Laforce. Frontiers in Neuroscience, 2026-02-20
Topic: Risk, prevention and care in population studies
Machine learning models consistently outperformed conventional approach. For the global detection of cognitive impairment, XGBoost achieved the best performance (Youden Index 0.61 vs. 0.54 for the standard cutoff). Regarding subtype classification, models demonstrated variable discriminative capacity depending on clinical homogeneity: primary progressive aphasia was best classified (Youden ≈ 0.77), followed by Lewy body dementia and Alzheimer's disease, while vascular dementia remained more challenging to isolate. Feature importance analysis highlighted the Cognitive Quotient as a robust universal predictor, while pinpointing disease-specific drivers such as delayed recall for Alzheimer's disease and verbal fluency for primary progressive aphasia. Our findings suggest interpretable machine learning enhances diagnostic utility of the MoCA, yielding superior accuracy compared to a fixed cutoff. By synthesizing individualized subtest profiles within a transparent framework, this approach offers a clinically actionable solution. It transforms the MoCA from a simple screening tool to a precision diagnostic aid, optimizing patient triage in the era of disease-modifying therapies.
Key findings
- Machine learning models consistently outperformed conventional approach.
- For the global detection of cognitive impairment, XGBoost achieved the best performance (Youden Index 0.61 vs. 0.54 for the standard cutoff).
- Regarding subtype classification, models demonstrated variable discriminative capacity depending on clinical homogeneity: primary progressive aphasia was best classified (Youden ≈ 0.77), followed by Lewy body dementia and Alzheimer's disease, while vascular dementia remained more challenging to isolate.
- Feature importance analysis highlighted the Cognitive Quotient as a robust universal predictor, while pinpointing disease-specific drivers such as delayed recall for Alzheimer's disease and verbal fluency for primary progressive aphasia.
- Our findings suggest interpretable machine learning enhances diagnostic utility of the MoCA, yielding superior accuracy compared to a fixed cutoff.
Why it matters
This study reports that machine learning models using MoCA test data performed better than the standard cutoff for detecting cognitive impairment and classifying subtypes. It is a diagnostic aid only and does not test any treatment, cure or prevention.
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Study details
- Participants38,746
- Evidence strengthLow
How this study scored 46/100
Published in a peer-reviewed journal. Scored zero for study design, effect reported and randomised / blinded because the record does not state it.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Frontiers in Neuroscience) |
| Journal's citation record | 2 / 4 | Frontiers in Neuroscience: journal h-index 226 (OpenAlex, 2026-10-29) |
| Study design | 0 / 12 | No study design recorded — scores zero, not guessed (not stated in the record — scored 0) |
| Strength of evidence | 1 / 5 | Rated “low” in our summary |
| Peer-review validation | 10 / 10 | Peer-reviewed. Published as an article in a named peer-reviewed journal. |
| How recent | 5 / 5 | 2026 — within 1 year(s) of the newest study here |
| Sample size | 4 / 4 | 38,746 participants |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 3 / 3 | Studied in people (participant count stated) |
| Randomised / blinded | 0 / 2 | No randomisation or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 1 / 7 | Cited 3 times (OpenAlex, 2026-10-10) |
| Citations per year | 1 / 5 | 1.5 citations a year over 2 year(s) since 2026 |
| Impact for its field and year | 4 / 6 | Cited 14.2× the average for papers of its field and year (OpenAlex FWCI) |
| Cited by studies here | 0 / 6 | No other study in this library cites it |
| Still being cited | 1 / 4 | Cited 3 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | 2 / 4 | Last-listed author Robert Jr Laforce: h-index 49 (OpenAlex, whole career) |
| Institution's track record | 0 / 3 | Centre hospitalier universitaire de Québec: institution h-index 345 (OpenAlex) |
| Multi-centre collaboration | 1 / 3 | OpenAlex lists 3 institution(s) in 1 country |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 41799879) |
| Free to read | 2 / 2 | Free to read |
| Total | 46 / 100 | — |
What each of these 20 components measures, and what this score is not →
Read the original
- DOI: 10.3389/fnins.2026.1679649
- PubMed: 41799879
- Original source →
- Free full text: Frontiers in Neuroscience →
Full text: free to read — OpenAlex lists this copy as free to read: the link above (checked 6 Feb 1020).
Cite this study APA, Vancouver, BibTeX · download .bib or .ris
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.
APA 7th
Gourdeau, C., Gourdeau, C. L., Bernier, P. J., & Laforce, R. J. (2026). Enhanced diagnostic interpretation of the MoCA using machine learning. Frontiers in Neuroscience. https://doi.org/10.3389/fnins.2026.1679649
Vancouver
Gourdeau C, Gourdeau CL, Bernier PJ, Laforce RJ. Enhanced diagnostic interpretation of the MoCA using machine learning. Frontiers in Neuroscience. 2026. doi:10.3389/fnins.2026.1679649. PMID: 41799879.
BibTeX
@article{gourdeau2026-41799879,
author = {Gourdeau, Christian and Gourdeau, Charles L. and Bernier, Patrick J. and Laforce, Robert Jr},
title = {{Enhanced diagnostic interpretation of the MoCA using machine learning}},
journal = {Frontiers in Neuroscience},
year = {2026},
doi = {10.3389/fnins.2026.1679649},
pmid = {41799879},
url = {https://doi.org/10.3389/fnins.2026.1679649}
}
Studies this one cites
Referenced by this study and also in the alzhub library, so you can read them here.