Evidence map›Paper›PMID 42317862›Full record

ArticleAMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science2026

Evaluating Representation Embeddings from LLMs and Time-Series Foundation Models for Wearable Accelerometer-Based Health Prediction.

Soomin You, Tian Gu

Abstract read
In one paragraph

Article in AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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.

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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

2 authors.

Soomin YouDepartment of Biostatistics, Columbia University Mailman School of Public Health, New York, NY.
Tian GuDepartment of Biostatistics, Columbia University Mailman School of Public Health, New York, NY.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wearable accelerometer data capture rich behavioral signals relevant for personalized health, yet the comparative evidence on modern representation-learning approaches remains limited. Using accelerometer data from the National Health and Nutrition Examination Survey (NHANES), we evaluated three representation families for predicting multiple clinical outcomes: simple entropy-based features, pretrained large-language-model (LLM) embeddings, and time-series foundation model embeddings. Outcomes included overweight status, lipid biomarkers, glucose, arthritis, and cancers. Across all endpoints, entropy-based features consistently performed comparably to, and often slightly better than, embedding approaches. LLM-derived embeddings offered only marginal improvements (ΔAUC≈0.01-0.05), and time-series foundation model embeddings provided minimal value across varying sequence lengths. Prompt-based LLM reasoning performed worst (AUC≈0.56-0.65), demonstrating limited ability to infer quantitative physiological states from structured text. These results highlight the strength of simple variability features and underscore the need for domain-aligned pretraining in future time-series foundation models for health sensing.

Identifiers

PMID42317862
PMCPMC13274337

What OpenQuestion holds

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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.