Automated body composition estimation from device-agnostic 3D optical scans in pediatric populations.


Journal

Clinical nutrition (Edinburgh, Scotland)
ISSN: 1532-1983
Titre abrégé: Clin Nutr
Pays: England
ID NLM: 8309603

Informations de publication

Date de publication:
09 2023
Historique:
received: 09 01 2023
revised: 19 05 2023
accepted: 12 07 2023
pmc-release: 01 09 2024
medline: 28 8 2023
pubmed: 24 7 2023
entrez: 23 7 2023
Statut: ppublish

Résumé

Excess adiposity in children is strongly correlated with obesity-related metabolic disease in adulthood, including diabetes, cardiovascular disease, and 13 types of cancer. Despite the many long-term health risks of childhood obesity, body mass index (BMI) Z-score is typically the only adiposity marker used in pediatric studies and clinical applications. The effects of regional adiposity are not captured in a single scalar measurement, and their effects on short- and long-term metabolic health are largely unknown. However, clinicians and researchers rarely deploy gold-standard methods for measuring compartmental fat such as magnetic resonance imaging (MRI) and dual X-ray absorptiometry (DXA) on children and adolescents due to cost or radiation concerns. Three-dimensional optical (3DO) scans are relatively inexpensive to obtain and use non-invasive and radiation-free imaging techniques to capture the external surface geometry of a patient's body. This 3D shape contains cues about the body composition that can be learned from a structured correlation between 3D body shape parameters and reference DXA scans obtained on a sample population. This study seeks to introduce a radiation-free, automated 3D optical imaging solution for monitoring body shape and composition in children aged 5-17. We introduce an automated, linear learning method to predict total and regional body composition of children aged 5-17 from 3DO scans. We collected 145 male and 206 female 3DO scans on children between the ages of 5 and 17 with three scanners from independent manufacturers. We used an automated shape templating method first introduced on an adult population to fit a topologically consistent 60,000 vertex (60 k) mesh to 3DO scans of arbitrary scanning source and mesh topology. We constructed a parameterized body shape space using principal component analysis (PCA) and estimated a regression matrix between the shape parameters and their associated DXA measurements. We automatically fit scans of 30 male and 38 female participants from a held-out test set and predicted 12 body composition measurements. The coefficient of determination (R Optical imaging can quickly, safely, and inexpensively estimate regional body composition in children aged 5-17. Frequent repeat measurements can be taken to chart changes in body adiposity over time without risk of radiation overexposure.

Sections du résumé

BACKGROUND
Excess adiposity in children is strongly correlated with obesity-related metabolic disease in adulthood, including diabetes, cardiovascular disease, and 13 types of cancer. Despite the many long-term health risks of childhood obesity, body mass index (BMI) Z-score is typically the only adiposity marker used in pediatric studies and clinical applications. The effects of regional adiposity are not captured in a single scalar measurement, and their effects on short- and long-term metabolic health are largely unknown. However, clinicians and researchers rarely deploy gold-standard methods for measuring compartmental fat such as magnetic resonance imaging (MRI) and dual X-ray absorptiometry (DXA) on children and adolescents due to cost or radiation concerns. Three-dimensional optical (3DO) scans are relatively inexpensive to obtain and use non-invasive and radiation-free imaging techniques to capture the external surface geometry of a patient's body. This 3D shape contains cues about the body composition that can be learned from a structured correlation between 3D body shape parameters and reference DXA scans obtained on a sample population.
STUDY AIM
This study seeks to introduce a radiation-free, automated 3D optical imaging solution for monitoring body shape and composition in children aged 5-17.
METHODS
We introduce an automated, linear learning method to predict total and regional body composition of children aged 5-17 from 3DO scans. We collected 145 male and 206 female 3DO scans on children between the ages of 5 and 17 with three scanners from independent manufacturers. We used an automated shape templating method first introduced on an adult population to fit a topologically consistent 60,000 vertex (60 k) mesh to 3DO scans of arbitrary scanning source and mesh topology. We constructed a parameterized body shape space using principal component analysis (PCA) and estimated a regression matrix between the shape parameters and their associated DXA measurements. We automatically fit scans of 30 male and 38 female participants from a held-out test set and predicted 12 body composition measurements.
RESULTS
The coefficient of determination (R
CONCLUSION
Optical imaging can quickly, safely, and inexpensively estimate regional body composition in children aged 5-17. Frequent repeat measurements can be taken to chart changes in body adiposity over time without risk of radiation overexposure.

Identifiants

pubmed: 37481870
pii: S0261-5614(23)00231-5
doi: 10.1016/j.clnu.2023.07.012
pmc: PMC10528749
mid: NIHMS1918617
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1619-1630

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK040561
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK111698
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK072476
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK109008
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD082166
Pays : United States

Informations de copyright

Copyright © 2023 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.

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Auteurs

Isaac Y Tian (IY)

Paul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA, 98195, USA. Electronic address: iytian@cs.washington.edu.

Michael C Wong (MC)

University of Hawaii Cancer Center, University of Hawaii - Manoa, Honolulu, HI, 96813, USA.

William M Nguyen (WM)

Paul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA, 98195, USA.

Samantha Kennedy (S)

Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA, 70808, USA.

Cassidy McCarthy (C)

Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA, 70808, USA.

Nisa N Kelly (NN)

University of Hawaii Cancer Center, University of Hawaii - Manoa, Honolulu, HI, 96813, USA.

Yong E Liu (YE)

University of Hawaii Cancer Center, University of Hawaii - Manoa, Honolulu, HI, 96813, USA.

Andrea K Garber (AK)

UCSF School of Medicine, University of California - San Francisco, San Francisco, CA, 94118, USA.

Steven B Heymsfield (SB)

Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA, 70808, USA.

Brian Curless (B)

Paul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA, 98195, USA.

John A Shepherd (JA)

University of Hawaii Cancer Center, University of Hawaii - Manoa, Honolulu, HI, 96813, USA.

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Classifications MeSH