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Blunted rest-activity rhythms link to higher body mass index and inflammatory markers in children
Jingyi Qian1,2, Nuria Martinez-Lozano3,4, Asta Tvarijonaviciute5
1Medical Chronobiology Program, Division of Sleep and Circadian Disorders, Departments of Medicine and Neurology, Brigham and Women's Hospital, Boston, MA.
Insights
Children with weaker rest-activity rhythms have higher BMI and inflammation. Improving these rhythms early may prevent childhood obesity and related inflammation.
Area of Science:
- Pediatric Health
- Chronobiology
- Obesity Research
Background:
- Disturbances in daily rest-activity patterns are linked to increased body mass index (BMI) in adults.
- The relationship between rest-activity rhythms and childhood obesity is not well understood.
- This study investigates the connection between rest-activity patterns and BMI in children.
Purpose of the Study:
- To examine the association between rest-activity rhythm characteristics and BMI z-score in school-aged children.
- To investigate the link between rest-activity rhythm metrics and obesity-related inflammatory markers in children.
- To explore potential early intervention strategies for childhood obesity.
Main Methods:
- 411 healthy Spanish children (mean age 10.1 years) wore accelerometers for 7 days.
- Rest-activity rhythm metrics were analyzed using parametric and nonparametric methods.
- Salivary inflammatory markers were measured in a subset of participants (n=121).
Main Results:
- Lower relative amplitude of rest-activity rhythms was associated with higher BMI z-score (p=0.02).
- This association remained significant after adjusting for sleep duration but attenuated after accounting for daytime activity.
- Less robust rhythms correlated with elevated pro-inflammatory markers, including C-reactive protein, independently of BMI and activity levels.
Conclusions:
- Blunted rest-activity rhythms are associated with higher BMI and pro-inflammatory markers in children.
- These associations appear independent of sleep duration and, for inflammation, also independent of daytime activity.
- Enhancing rest-activity rhythm strength in early life may offer a novel target for preventing childhood obesity and associated inflammation.
Study Objectives:
Disturbances of rest-activity rhythms are associated with higher body mass index (BMI) in adults. Whether such relationship exists in children is unclear. We aimed to examine cross-sectional associations of rest-activity rhythm characteristics with BMI z-score and obesity-related inflammatory markers in school-age children.
Methods:
Participants included 411 healthy children (mean ± SD age 10.1 ± 1.3 years, 50.8% girls) from a Mediterranean area of Spain who wore wrist accelerometers for 7 consecutive days. Metrics of rest-activity rhythm were derived using both parametric and nonparametric approaches. Obesity-related inflammatory markers were measured in saliva (n = 121).
Results:
In a multivariable-adjusted model, higher BMI z-score is associated with less robust 24-h rest-activity rhythms as represented by lower relative amplitude (-0.16 [95% CI -0.29, -0.02] per SD, p = 0.02). The association between BMI z-score and relative amplitude persisted with additional adjustment for sleep duration, and attenuated after adjustment for daytime activity level. Less robust rest-activity rhythms were related to increased levels of several salivary pro-inflammatory markers, including C-reactive protein, which is inversely associated with relative amplitude (-32.6% [-47.8%, -12.9%] per SD), independently of BMI z-score, sleep duration, and daytime activity level.
Conclusion:
Blunted rest-activity rhythms are associated with higher BMI z-score and salivary pro-inflammatory markers already at an early age. The association with BMI z-score seem to be independent of sleep duration, and those with pro-inflammatory markers further independent of BMI z-score and daytime activity. Novel intervention targets at an early age based on improving the strength of rest-activity rhythms may help to prevent childhood obesity and related inflammation.
Clinical Trials Registration:
NCT02895282.
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