Comparing Human-Smartphone Interactions and Actigraphy Measurements for Circadian Rhythm Stability and Adiposity: Algorithm Development and Validation Study.


Journal

Journal of medical Internet research
ISSN: 1438-8871
Titre abrégé: J Med Internet Res
Pays: Canada
ID NLM: 100959882

Informations de publication

Date de publication:
05 Jun 2024
Historique:
received: 21 06 2023
accepted: 20 03 2024
revised: 17 11 2023
medline: 5 6 2024
pubmed: 5 6 2024
entrez: 5 6 2024
Statut: epublish

Résumé

This study aimed to investigate the relationships between adiposity and circadian rhythm and compare the measurement of circadian rhythm using both actigraphy and a smartphone app that tracks human-smartphone interactions. We hypothesized that the app-based measurement may provide more comprehensive information, including light-sensitive melatonin secretion and social rhythm, and have stronger correlations with adiposity indicators. We enrolled a total of 78 participants (mean age 41.5, SD 9.9 years; 46/78, 59% women) from both an obesity outpatient clinic and a workplace health promotion program. All participants (n=29 with obesity, n=16 overweight, and n=33 controls) were required to wear a wrist actigraphy device and install the Rhythm app for a minimum of 4 weeks, contributing to a total of 2182 person-days of data collection. The Rhythm app estimates sleep and circadian rhythm indicators by tracking human-smartphone interactions, which correspond to actigraphy. We examined the correlations between adiposity indices and sleep and circadian rhythm indicators, including sleep time, chronotype, and regularity of circadian rhythm, while controlling for physical activity level, age, and gender. Sleep onset and wake time measurements did not differ significantly between the app and actigraphy; however, wake after sleep onset was longer (13.5, SD 19.5 minutes) with the app, resulting in a longer actigraphy-measured total sleep time (TST) of 20.2 (SD 66.7) minutes. The obesity group had a significantly longer TST with both methods. App-measured circadian rhythm indicators were significantly lower than their actigraphy-measured counterparts. The obesity group had significantly lower interdaily stability (IS) than the control group with both methods. The multivariable-adjusted model revealed a negative correlation between BMI and app-measured IS (P=.007). Body fat percentage (BF%) and visceral adipose tissue area (VAT) showed significant correlations with both app-measured IS and actigraphy-measured IS. The app-measured midpoint of sleep showed a positive correlation with both BF% and VAT. Actigraphy-measured TST exhibited a positive correlation with BMI, VAT, and BF%, while no significant correlation was found between app-measured TST and either BMI, VAT, or BF%. Our findings suggest that IS is strongly correlated with various adiposity indicators. Further exploration of the role of circadian rhythm, particularly measured through human-smartphone interactions, in obesity prevention could be warranted.

Sections du résumé

BACKGROUND BACKGROUND
This study aimed to investigate the relationships between adiposity and circadian rhythm and compare the measurement of circadian rhythm using both actigraphy and a smartphone app that tracks human-smartphone interactions.
OBJECTIVE OBJECTIVE
We hypothesized that the app-based measurement may provide more comprehensive information, including light-sensitive melatonin secretion and social rhythm, and have stronger correlations with adiposity indicators.
METHODS METHODS
We enrolled a total of 78 participants (mean age 41.5, SD 9.9 years; 46/78, 59% women) from both an obesity outpatient clinic and a workplace health promotion program. All participants (n=29 with obesity, n=16 overweight, and n=33 controls) were required to wear a wrist actigraphy device and install the Rhythm app for a minimum of 4 weeks, contributing to a total of 2182 person-days of data collection. The Rhythm app estimates sleep and circadian rhythm indicators by tracking human-smartphone interactions, which correspond to actigraphy. We examined the correlations between adiposity indices and sleep and circadian rhythm indicators, including sleep time, chronotype, and regularity of circadian rhythm, while controlling for physical activity level, age, and gender.
RESULTS RESULTS
Sleep onset and wake time measurements did not differ significantly between the app and actigraphy; however, wake after sleep onset was longer (13.5, SD 19.5 minutes) with the app, resulting in a longer actigraphy-measured total sleep time (TST) of 20.2 (SD 66.7) minutes. The obesity group had a significantly longer TST with both methods. App-measured circadian rhythm indicators were significantly lower than their actigraphy-measured counterparts. The obesity group had significantly lower interdaily stability (IS) than the control group with both methods. The multivariable-adjusted model revealed a negative correlation between BMI and app-measured IS (P=.007). Body fat percentage (BF%) and visceral adipose tissue area (VAT) showed significant correlations with both app-measured IS and actigraphy-measured IS. The app-measured midpoint of sleep showed a positive correlation with both BF% and VAT. Actigraphy-measured TST exhibited a positive correlation with BMI, VAT, and BF%, while no significant correlation was found between app-measured TST and either BMI, VAT, or BF%.
CONCLUSIONS CONCLUSIONS
Our findings suggest that IS is strongly correlated with various adiposity indicators. Further exploration of the role of circadian rhythm, particularly measured through human-smartphone interactions, in obesity prevention could be warranted.

Identifiants

pubmed: 38838328
pii: v26i1e50149
doi: 10.2196/50149
doi:

Types de publication

Journal Article Comparative Study Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e50149

Informations de copyright

©Hai-Hua Chuang, Chen Lin, Li-Ang Lee, Hsiang-Chih Chang, Guan-Jie She, Yu-Hsuan Lin. Originally published in the Journal of Medical Internet Research (https://www.jmir.org), 05.06.2024.

Auteurs

Hai-Hua Chuang (HH)

College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Department of Family Medicine, Chang Gung Memorial Hospital, Linkou Main Branch, Taoyuan, Taiwan.
Department of Industrial Engineering and Management, National Taipei University of Technology, Taipei, Taiwan.
School of Medicine, National Tsing Hua University, Hsinchu, Taiwan.

Chen Lin (C)

Department of Biomedical Sciences and Engineering, National Central University, Taoyuan City, Taiwan.

Li-Ang Lee (LA)

College of Medicine, Chang Gung University, Taoyuan, Taiwan.
School of Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Department of Otorhinolaryngology - Head and Neck Surgery, Chang Gung Memorial Hospital, Linkou Main Branch, Taoyuan, Taiwan.

Hsiang-Chih Chang (HC)

Institute of Population Health Sciences, National Health Research Institutes, Miaoli County, Taiwan.

Guan-Jie She (GJ)

Institute of Population Health Sciences, National Health Research Institutes, Miaoli County, Taiwan.

Yu-Hsuan Lin (YH)

Institute of Population Health Sciences, National Health Research Institutes, Miaoli County, Taiwan.
Department of Psychiatry, National Taiwan University Hospital, Taipei, Taiwan.
Department of Psychiatry, College of Medicine, National Taiwan University, Taipei, Taiwan.

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