Publication

Metabolic flexibility differs by body composition in adults

Downloadable Content

Persistent URL
Last modified
  • 09/19/2025
Type of Material
Authors
    Siran He, Emory UniversityNgoc-Anh Le, VA Medical CenterManuel Ramírez-Zea, Institute of Nutrition of Central America and Panama GuatemalaReynaldo Martorell, Emory UniversityVenkat KM Narayan, Emory UniversityAryeh Stein, Emory University
Language
  • English
Date
  • 2021-12-01
Publisher
  • Elsevier Inc.
Publication Version
Copyright Statement
  • Published by Elsevier B.V. on behalf of International Federation of Clinical Neurophysiology.
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 46
Start Page
  • 372
End Page
  • 379
Grant/Funding Information
  • This work was supported by the National Institutes of Health (Grant No. HD075784). The funding agency had no involvement in the study design, in the collection, analysis, and interpretation of data, in the writing of the report, nor in the decision to submit the article for publication.
Supplemental Material (URL)
Abstract
  • Background & aims: With the rise of global cardiometabolic diseases, it is important to investigate risk factors such as obesity. Metabolic flexibility, the ability to maintain metabolic homeostasis following an acute challenge, can reflect cardiometabolic health. We investigated the association between body composition and the metabolic flexibility following meal consumption in an adult population. Methods: In this study of 1027 participants (mean age 44.0 y ± SD 4.2 y), we administered a mixed-macronutrient meal challenge. Fasting and 2-h postprandial plasma were assayed for lipids, glycemic, and inflammation biomarkers. We characterized metabolic flexibility through meal-induced biomarker responses (%Δ, the difference between postprandial and fasting concentrations, divided by fasting concentration). We then compared the responses by sex-specific tertiles of body mass index (BMI) and percent body fat. Results: With every unit (kg/m2) increase in BMI, %Δ (95% confidence interval) increased by 0.17% (0.09, 0.26%) for total cholesterol, 0.31% (0.07, 0.54%) for triglycerides, and 0.11% (0.01, 0.20%) for apoA-I, whereas insulin elevation was reduced (−6.30%; −8.41, −4.20%), and the reduction in leptin was attenuated (0.64%; 0.25, 1.05%). With each unit (percent) increase in body fat, we observed similar changes in the %Δ of total cholesterol and leptin but not in triglycerides, apoA-I, or insulin. Glucose response increased by 0.29% (0.06, 0.51%) as body fat increases by one unit. Conclusion: Metabolic flexibility, as assessed by biomarker responses to an acute physiological meal challenge, differed by body composition. These findings may help elucidate the pathways through which obesity contributes to cardiometabolic diseases.
Author Notes
  • Aryeh D. Stein, PhD, MPH, Mailing address: Room 7007, 1518 Clifton Rd NE, Atlanta GA 30322, Telephone: (+1) 404 727 4255. Email: aryeh.stein@emory.edu
Keywords

Tools

Relations

In Collection:

Items