Effects of Moderate and Subsequent Progressive Weight Loss on Metabolic Function and Adipose Tissue Biology in Humans with Obesity

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Effects of Moderate and Subsequent Progressive Weight Loss on Metabolic Function and Adipose Tissue Biology in Humans with Obesity
Title:
Effects of Moderate and Subsequent Progressive Weight Loss on Metabolic Function and Adipose Tissue Biology in Humans with Obesity
Journal Title:
Cell Metabolism
OA Status:
Keywords:
Publication Date:
22 February 2016
Citation:
Magkos F, Fraterrigo G, Yoshino J, et al. Effects of Moderate and Subsequent Progressive Weight Loss on Metabolic Function and Adipose Tissue Biology in Humans with Obesity. Cell Metab. 2016;23(4):591‐601. doi:10.1016/j.cmet.2016.02.005
Abstract:
Although 5%-10% weight loss is routinely recommended for people with obesity, the precise effects of 5% and further weight loss on metabolic health are unclear. We conducted a randomized controlled trial that evaluated the effects of 5.1% ± 0.9% (n = 19), 10.8% ± 1.3% (n = 9), and 16.4% ± 2.1% (n = 9) weight loss and weight maintenance (n = 14) on metabolic outcomes. 5% weight loss improved adipose tissue, liver and muscle insulin sensitivity, and β cell function, without a concomitant change in systemic or subcutaneous adipose tissue markers of inflammation. Additional weight loss further improved β cell function and insulin sensitivity in muscle and caused stepwise changes in adipose tissue mass, intrahepatic triglyceride content, and adipose tissue expression of genes involved in cholesterol flux, lipid synthesis, extracellular matrix remodeling, and oxidative stress. These results demonstrate that moderate 5% weight loss improves metabolic function in multiple organs simultaneously, and progressive weight loss causes dose-dependent alterations in key adipose tissue biological pathways.
License type:
PublisherCopyrights
Funding Info:
This study was supported by National Institutes of Health grants DK 37948, DK 104995, DK 56341 (Nutrition Obesity Research Center), DK20579 (Diabetes Research Center) and RR024992 (Clinical and Translational Science Award), a KL2 Career Development Award (TR 000450), and grants from the Pershing Square Foundation and the Longer Life Foundation.
Description:
The full paper is available for download at the publisher's URL: https://doi.org/10.1016/j.cmet.2016.02.005
ISSN:
1550-4131
1932-7420
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