Associations between eating behaviours and cardiometabolic risk among adolescents in the Health Outcomes and Measures of the Environment study
- PMID: 36094787
- PMCID: PMC10392767
- DOI: 10.1111/ijpo.12979
Associations between eating behaviours and cardiometabolic risk among adolescents in the Health Outcomes and Measures of the Environment study
Abstract
Background: Eating behaviours are associated with childhood obesity, but their associations with cardiometabolic risk are less clear.
Objectives: We evaluated cross-sectional associations between eating behaviours and cardiometabolic risk among 185 adolescents (age 12.4 ± 0.7 years; 53% female; body mass index (BMI)-z 0.72 ± 1.37) from Cincinnati, Ohio (HOME Study; enrolled 2003-2006).
Methods: Caregivers assessed adolescents' eating behaviours with the Child Eating Behaviour Questionnaire. We computed adolescents' cardiometabolic risk scores based on HOMA-IR, triglycerides to high-density lipoprotein cholesterol ratio, adiponectin to leptin ratio, systolic blood pressure, and cross-sectional area of fat inside the abdominal cavity. Using multivariable linear regression models, we estimated associations of eating behaviour subscales with cardiometabolic risk scores or individual risk components.
Results: Emotional overeating (ß = 1.34, 95% CI: 0.67, 2.01), food responsiveness (ß = 0.99, 95% CI: 0.41, 1.57), and emotional undereating (ß = 0.64, 95% CI: 0.08, 1.21) were associated with higher cardiometabolic risk scores. Satiety responsiveness (ß = -0.79, 95% CI: -1.59, 0.00) was associated with lower cardiometabolic risk scores. Adjusting for adolescent BMI-z at age 12 attenuated these associations, suggesting that adiposity may mediate these associations.
Conclusion: Hedonistic eating behaviours were associated with higher cardiometabolic risk in these adolescents.
Keywords: adolescents; cardiometabolic risk; eating behaviours; epidemiology; prevention.
© 2022 World Obesity Federation.
Conflict of interest statement
Conflicts of Interest Statement
JMB was financially compensated for his services as an expert witness for plaintiffs in litigation related to PFAS-contaminated drinking water. KMC was a Joint Steering Committee Member for the Vigilan Study of Creatine Transporter Deficiency and served on the Advisory Council for the American Society of Neuroradiology, which had no role in this research. CBE was financially compensated for his services as an expert witness for plaintiffs in litigation related to PFAS-contaminated drinking water. The other authors report no actual or potential conflicts of interest.
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