Evidence map›Paper›PMID 41264615›Full record

ArticlePLOS digital health2025

Longitudinal wearable sensor data enhance precision of Long COVID detection.

Chibuike K Uwakwe, Ekanath Srihari Rangan, Satyajit Kumar, Georg Gutjahr, Xuhui Miao, Andrew W Brooks, Peter Maguire, Tejaswini Mishra, Lettie McGuire, Michael P Snyder

Abstract read
In one paragraph

Article in PLOS digital health, 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

10 authors.

Chibuike K UwakweDepartment of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0002-5963-4943
Ekanath Srihari RanganDepartment of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, United States of America.
Satyajit KumarDepartment of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, United States of America.
Georg GutjahrDepartment of Health Science Research, School of Medicine, Amrita Vishwa Vidyapeetham University, Kochi, Kerala, India.
Xuhui MiaoDepartment of Computer Science, School of Engineering, Stanford University, Stanford, California, United States of America.
Andrew W BrooksDepartment of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, United States of America.
Peter MaguireDepartment of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, United States of America.
Tejaswini MishraDepartment of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0001-9931-1260
Lettie McGuireDepartment of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, United States of America.ORCID https://orcid.org/0000-0003-0899-3521
Michael P SnyderDepartment of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, United States of America.

Funding

Spectrum Stanford Center for clinical and Translational Research and EducationUL1TR001085 · NCATS · STANFORD UNIVERSITY · PI CULLEN, MARK RICHARD, GREENBERG, HARRY BERNARD · 2013 to 2017
$37.1M
Computational appliance: a supercomputer for modern biomedical researchS10OD023452 · OD · STANFORD UNIVERSITY · PI DATTA, SOMALEE · 2017 to 2017
$600k
NCATS NIH HHS UL1 TR001085NIH HHS S10 OD023452
6 · The paper itself

Abstract

Despite the millions of individuals struggling with persistent symptoms, Long COVID has remained difficult to diagnose due to limited objective biomarkers, often leading to underdiagnosis or even misdiagnosis. To bridge this gap, we investigated the potential of utilizing wearable sensor data to aid in the diagnosis of Long COVID. We analyzed longitudinal heart rate (HR) data from 126 individuals with acute SARS-CoV-2 infections to develop machine learning models capable of predicting Long COVID status using derived HR features, symptom features, or a combination of both feature sets. The HR features were derived across six analytical categories, including time-domain, Poincaré nonlinear, raw signal, Kullback-Leibler (KL) divergence, variational mode decomposition (VMD), and the Shannon energy envelope (SEE), enabling the capture of heart rate dynamics over various temporal scales and the quantification of day-to-day shifts in HR distributions. The symptom features used in the final models included chest pain, vomiting, excessive sweating, memory loss, brain fog, heart palpitations, and loss of smell. The combined HR- and symptom-feature model demonstrated robust predictive performance, achieving an area under the Receiver Operating Characteristic curve (ROC-AUC) of 95.1% and an area under the Precision-Recall curve (PR-AUC) of 85.9%. These values represent a significant improvement of approximately 5% in both the ROC-AUC and PR-AUC over the symptoms-only model. At the population level, this improvement in discrimination could lead to clinically meaningful reductions in misclassification and improved patient outcomes, achieved through a non-invasive diagnostic tool. These findings suggest that wearable HR data could be used to derive an objective biomarker for Long COVID, thereby enhancing diagnostic precision.

Identifiers

PMID41264615
PMCPMC12633932

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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.