Evidence map›Paper›PMID 42453495›Full record

ArticleNeurology open access2025

Facial Expression Metrics as Digital Biomarkers of Neurologic Disease.

Alyssa Nylander, Shane Poole, Nathan S Hsu, Kyra Henderson, Nikki Sisodia, Jaeleene Wijangco, Jim Rowson, Cathra Halabi, Jill L Ostrem, Simon Little and 3 more

Abstract read
In one paragraph

Article in Neurology open access, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Alyssa NylanderUniversity of California San Francisco, Division of Neuroimmunology and Glial Biology.
Shane PooleUniversity of California San Francisco, Division of Neuroimmunology and Glial Biology.
Nathan S HsuUniversity of California San Francisco, Division of Neuroimmunology and Glial Biology.
Kyra HendersonUniversity of California San Francisco, Division of Neuroimmunology and Glial Biology.
Nikki SisodiaUniversity of California San Francisco, Division of Neuroimmunology and Glial Biology.
Jaeleene WijangcoUniversity of California San Francisco, Division of Neuroimmunology and Glial Biology.
Jim RowsonUniversity of California San Francisco, Division of Neuroimmunology and Glial Biology.
Cathra HalabiUniversity of California, San Francisco, Division of Neurovascular.
Jill L OstremUniversity of California, San Francisco, Movement Disorders and Neuromodulation Center.
Simon LittleUniversity of California, San Francisco, Movement Disorders and Neuromodulation Center.
Ethan BrownUniversity of California, San Francisco, Movement Disorders and Neuromodulation Center.
Adam StaffaroniUniversity of California, San Francisco, Memory and Aging Center.
Riley BoveUniversity of California San Francisco, Division of Neuroimmunology and Glial Biology.

Funding

Assessing Cognitive Overload in People with Multiple SclerosisK23HD116016 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ALYSSA Nicole NYLANDER · 2025 to 2026
$346k
NICHD NIH HHS K23 HD116016
6 · The paper itself

Abstract

Background and Objectives: Facial movements can be key indicators of neurological health and emotional state, offering insights into motor and neuropsychiatric functions that are disrupted in neurologic disorders. Neurological disease can present with characteristic differences in facial movements, like the masked facies of parkinsonism. Automated digital facial expression recognition could assist in asynchronous, remote and objective diagnostic processes. We hypothesized that facial movements relating to smiling, frowning, and blinking could be extracted from brief video-taped encounters in a clinic setting and used to (1) differentiate between neurologic diagnoses, and (2) identify people with symptoms of anxiety and depression. Methods: Using untargeted recruitment, individuals with multiple sclerosis (MS), other conditions (parkinsonism, frontotemporal dementia (FTD)), and healthy controls (HC) enrolled in an ongoing digital phenotyping study. Participant faces were video-recorded during a spontaneous language task. Videos were processed using OpenFace 2.2.0, an open-access digital tool pre-trained for facial landmark detection and facial action unit recognition. Participants with MS completed the General Anxiety Disorder-7 (GAD-7) and the Hospital Anxiety and Depression Scale (HADS-D). Results: Videos were analyzed for adults with MS (n=151, mean age 48, 72% female), parkinsonism (n=23, mean age 67, 35% female), FTD (n=14, mean age 68, 29% female), and HCs (n=33, mean age 55, 58% female). Sampling duration was 60-90 seconds; 91% videos passed quality control. Individuals with parkinsonism had decreased eye-blinking compared to all groups, and decreased smiling and increased brow-lowering compared to MS and HCs. Individuals with FTD had increased blinking relative to other groups. There were no significant differences between individuals with MS and HCs. Classification accuracy for partition analysis model was 88% (ROC-AUC 0.84 for parkinsonism). In individuals with MS, decreased variability in brow lowerering was seen with higher anxiety symptoms, and decreased cheek raising intensity was seen with higher depression symptoms. Interpretation: Digitally identified facial movements have face validity for recapitulating known clinical characteristics of neurological disease, as well as reflecting internal state relating to mood. This provides a foundation for expanded longitudinal validation of computer vision-based facial movement analysis in neurological research. However, findings should be interpreted in the context of sample size imbalance across diagnostic groups, which may have influenced classification performance.

Identifiers

PMID42453495
PMCPMC13367924

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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.