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Metabolic flexibility across the spectrum of glycemic regulation in youth
BACKGROUND: Metabolic flexibility (MF) refers to the relative ability to utilize lipid and carbohydrate substrates and to transition between them. It is not clear whether MF is impaired in obese youth and what the determining factors are. METHODS: We investigated the determinants of MF (increased re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Clinical Investigation
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934924/ https://www.ncbi.nlm.nih.gov/pubmed/33616083 http://dx.doi.org/10.1172/jci.insight.146000 |
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author | Bacha, Fida Bartz, Sara Klinepeter Puyau, Maurice Adolph, Anne Sharma, Susan |
author_facet | Bacha, Fida Bartz, Sara Klinepeter Puyau, Maurice Adolph, Anne Sharma, Susan |
author_sort | Bacha, Fida |
collection | PubMed |
description | BACKGROUND: Metabolic flexibility (MF) refers to the relative ability to utilize lipid and carbohydrate substrates and to transition between them. It is not clear whether MF is impaired in obese youth and what the determining factors are. METHODS: We investigated the determinants of MF (increased respiratory exchange ratio [ΔRER] under insulin-stimulated conditions) in pubertal youth (n = 104; 15.6 ± 1.8 years) with obesity across the spectrum of glucose tolerance compared with normal weight (NW) controls, including body composition (fat-free mass [FFM], %body fat), visceral adipose fat (VAT) (MRI), glycemia, and insulin sensitivity (IS) [3-hour hyperinsulinemic-euglycemic clamp with measurement of lipolysis ([(2)H(5)] glycerol), free fatty acids (FFAs), and RER (indirect calorimetry)]. RESULTS: Youth with prediabetes and type 2 diabetes had lower ΔRER and oxidative and nonoxidative glucose disposal compared with NW, with no significant difference in ΔRER between NW and obese with normal glucose tolerance. In multiple regression analysis, IS(FFM) (β = 0.4, P = 0.004), percentage suppression of FFAs (r = 0.26, P = 0.007), and race/ethnicity (β = –0.23, P = 0.02) contributed to the variance in ΔRER (R(2) = 0.30, P < 0.001) independent of percentage body fat (or VAT), sex, Tanner stage, and hemoglobin A1c. CONCLUSION: MF is defective at the extreme of the metabolic phenotype in obese youth with dysglycemia related to a defect in IS limiting substrate utilization. FUNDING: USDA/ARS Project Number 3092-51000-057. |
format | Online Article Text |
id | pubmed-7934924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-79349242021-03-09 Metabolic flexibility across the spectrum of glycemic regulation in youth Bacha, Fida Bartz, Sara Klinepeter Puyau, Maurice Adolph, Anne Sharma, Susan JCI Insight Clinical Medicine BACKGROUND: Metabolic flexibility (MF) refers to the relative ability to utilize lipid and carbohydrate substrates and to transition between them. It is not clear whether MF is impaired in obese youth and what the determining factors are. METHODS: We investigated the determinants of MF (increased respiratory exchange ratio [ΔRER] under insulin-stimulated conditions) in pubertal youth (n = 104; 15.6 ± 1.8 years) with obesity across the spectrum of glucose tolerance compared with normal weight (NW) controls, including body composition (fat-free mass [FFM], %body fat), visceral adipose fat (VAT) (MRI), glycemia, and insulin sensitivity (IS) [3-hour hyperinsulinemic-euglycemic clamp with measurement of lipolysis ([(2)H(5)] glycerol), free fatty acids (FFAs), and RER (indirect calorimetry)]. RESULTS: Youth with prediabetes and type 2 diabetes had lower ΔRER and oxidative and nonoxidative glucose disposal compared with NW, with no significant difference in ΔRER between NW and obese with normal glucose tolerance. In multiple regression analysis, IS(FFM) (β = 0.4, P = 0.004), percentage suppression of FFAs (r = 0.26, P = 0.007), and race/ethnicity (β = –0.23, P = 0.02) contributed to the variance in ΔRER (R(2) = 0.30, P < 0.001) independent of percentage body fat (or VAT), sex, Tanner stage, and hemoglobin A1c. CONCLUSION: MF is defective at the extreme of the metabolic phenotype in obese youth with dysglycemia related to a defect in IS limiting substrate utilization. FUNDING: USDA/ARS Project Number 3092-51000-057. American Society for Clinical Investigation 2021-02-22 /pmc/articles/PMC7934924/ /pubmed/33616083 http://dx.doi.org/10.1172/jci.insight.146000 Text en © 2021 Bacha et al. http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Medicine Bacha, Fida Bartz, Sara Klinepeter Puyau, Maurice Adolph, Anne Sharma, Susan Metabolic flexibility across the spectrum of glycemic regulation in youth |
title | Metabolic flexibility across the spectrum of glycemic regulation in youth |
title_full | Metabolic flexibility across the spectrum of glycemic regulation in youth |
title_fullStr | Metabolic flexibility across the spectrum of glycemic regulation in youth |
title_full_unstemmed | Metabolic flexibility across the spectrum of glycemic regulation in youth |
title_short | Metabolic flexibility across the spectrum of glycemic regulation in youth |
title_sort | metabolic flexibility across the spectrum of glycemic regulation in youth |
topic | Clinical Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934924/ https://www.ncbi.nlm.nih.gov/pubmed/33616083 http://dx.doi.org/10.1172/jci.insight.146000 |
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