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Erik A Imel

Professor

Indiana University School of Medicine
Country flagUnited States

Research Interests

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Articles (9)

Year:

2026

Year:

2026

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Introduction Sarcopenia (low muscle mass and strength) causes dysmobility and loss of independence. Sarcopenia is often not directly coded or described in electronic health records (EHR). The objective was to improve sarcopenia detection using structured data from EHR. Methods Adults undergoing musculoskeletal testing (December 2017–March 2020) were classified as meeting sarcopenia thresholds for 0 (controls), ≥1 (Sarcopenia-1), or ≥2 (Sarcopenia-2) tests. Electronic health record diagnoses, medications, and laboratory testing were extracted from the Indiana Network for Patient Care. Five machine learning models were applied to EHR data for predicting sarcopenia. Results Of 1304 participants, 1055 were controls, 249 met Sarcopenia-1 and 76 met Sarcopenia-2. Sarcopenic participants were older, with higher fat mass, Charlson Comorbidity Index, and more chronic diseases. All models performed better for Sarcopenia-2 than Sarcopenia-1. The top performing models for Sarcopenia-1 were Logistic Regression [area under the curve (AUC) 71.59 (95% confidence interval [CI], 71.51–71.66)] and Multi-Layer Perceptron [AUC 71.48 (95%CI, 71.00–71.97)]. The top performing models for Sarcopenia-2 were Logistic Regression [AUC 91.44 (95%CI, 91.28–91.60)] and Support Vector Machine [AUC 90.81 (95%CI, 88.41–93.20)]. For the best Logistic Regression Model, important sarcopenia predictors included diabetes mellitus, digestive system complaints, signs and symptoms involving the nervous, musculoskeletal and respiratory systems, metabolic disorders, and kidney or urinary tract disorders. Opioids, corticosteroids, and antihyperlipidemic drugs were also more common among sarcopenic participants. Conclusions Applying machine learning models, sarcopenia can be predicted from structured data in EHR, which may be developed through future studies to facilitate large-scale early detection and intervention in clinical populations.

Year:

2023

Collaborators (13)

Signe Beck-Nielsen

Aarhus University

DENMARK
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Suma Uday

University of Birmingham

UNITED KINGDOM
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Stuart Warden

Chancellor's Professor

Indiana University-Purdue University Indianapolis

UNITED STATES
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Seiji Fukumoto

Tokushima University

JAPAN
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Thomas O Carpenter

Yale University School of Medicine

UNITED STATES
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Catherine Chaussain

Prof

Université Paris Cité

FRANCE
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Sharon M Moe

-

UNITED STATES
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Robyn K Fuchs

Professor of Physiology

Marian University

UNITED STATES
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Jill Simmons

Professor

Vanderbilt University

UNITED STATES
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Rachel Surowiec

Assistant Professor

Purdue University

UNITED STATES
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Rachel Crowley

St. Vincent's University Hospital

IRELAND
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Paul Goodyer

Professor

McGill University

CANADA
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Natasha M. Appelman‐Dijkstra

Endocrinologist

Leiden University Medical Center

NETHERLANDS
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