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Testing for Protein Leverage in Patients with Gastric Bypass: A Pilot Study
INTRODUCTION: Protein leverage (PL) is the phenomenon whereby a dominant appetite for protein drives overconsumption of energy with a decline in the ratio of protein to fat and carbohydrate in the diet. PL has been independently verified in several randomized control trials, and its predictions are...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10614273/ https://www.ncbi.nlm.nih.gov/pubmed/37536296 http://dx.doi.org/10.1159/000532125 |
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author | Rodriguez-Murguia, Nantli Malacara, Juan M. Kusnir, Daniel Siniego, Alberto Melendez-Rios, Dora Raubenheimer, David Simpson, Stephen Martinez-Cordero, Claudia |
author_facet | Rodriguez-Murguia, Nantli Malacara, Juan M. Kusnir, Daniel Siniego, Alberto Melendez-Rios, Dora Raubenheimer, David Simpson, Stephen Martinez-Cordero, Claudia |
author_sort | Rodriguez-Murguia, Nantli |
collection | PubMed |
description | INTRODUCTION: Protein leverage (PL) is the phenomenon whereby a dominant appetite for protein drives overconsumption of energy with a decline in the ratio of protein to fat and carbohydrate in the diet. PL has been independently verified in several randomized control trials, and its predictions are supported by diet surveillance data. Our aim in the present study was to test whether surgical intervention through gastric bypass will ameliorate the PL effect. METHODS: Ten patients with gastric bypass (2–5 years postsurgical time) were given ad libitum access to study food comprising 10%, 15%, or 25% protein and no access to other foods for 3 days while controlling food palatability and variety. Food intake was measured, and energy and nutrient intakes were calculated. Body weight, blood chemistry, lipid profile, hormones (insulin, leptin, and ghrelin), and creatinine were determined before and after each experimental period. RESULTS: The gastric bypass patients in our study did not show evidence for protein intake regulation as predicted under PL but ate to constant total energy intake on the 10%, 15%, and 25% protein diets with protein intake varying significantly. Patients lost weight in the three study periods, but significant weight loss was observed only on the 15% protein diet. CONCLUSION: Our results suggest that gastric bypass might disengage the PL mechanism, thus ameliorating an appetite-specific mechanism that drives energy overconsumption in modern food environments. |
format | Online Article Text |
id | pubmed-10614273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-106142732023-10-31 Testing for Protein Leverage in Patients with Gastric Bypass: A Pilot Study Rodriguez-Murguia, Nantli Malacara, Juan M. Kusnir, Daniel Siniego, Alberto Melendez-Rios, Dora Raubenheimer, David Simpson, Stephen Martinez-Cordero, Claudia Ann Nutr Metab Human Nutrition: Research Article INTRODUCTION: Protein leverage (PL) is the phenomenon whereby a dominant appetite for protein drives overconsumption of energy with a decline in the ratio of protein to fat and carbohydrate in the diet. PL has been independently verified in several randomized control trials, and its predictions are supported by diet surveillance data. Our aim in the present study was to test whether surgical intervention through gastric bypass will ameliorate the PL effect. METHODS: Ten patients with gastric bypass (2–5 years postsurgical time) were given ad libitum access to study food comprising 10%, 15%, or 25% protein and no access to other foods for 3 days while controlling food palatability and variety. Food intake was measured, and energy and nutrient intakes were calculated. Body weight, blood chemistry, lipid profile, hormones (insulin, leptin, and ghrelin), and creatinine were determined before and after each experimental period. RESULTS: The gastric bypass patients in our study did not show evidence for protein intake regulation as predicted under PL but ate to constant total energy intake on the 10%, 15%, and 25% protein diets with protein intake varying significantly. Patients lost weight in the three study periods, but significant weight loss was observed only on the 15% protein diet. CONCLUSION: Our results suggest that gastric bypass might disengage the PL mechanism, thus ameliorating an appetite-specific mechanism that drives energy overconsumption in modern food environments. S. Karger AG 2023-08-03 2023-11 /pmc/articles/PMC10614273/ /pubmed/37536296 http://dx.doi.org/10.1159/000532125 Text en © 2023 The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution 4.0 International License (CC BY) (http://www.karger.com/Services/OpenAccessLicense). Usage, derivative works and distribution are permitted provided that proper credit is given to the author and the original publisher. |
spellingShingle | Human Nutrition: Research Article Rodriguez-Murguia, Nantli Malacara, Juan M. Kusnir, Daniel Siniego, Alberto Melendez-Rios, Dora Raubenheimer, David Simpson, Stephen Martinez-Cordero, Claudia Testing for Protein Leverage in Patients with Gastric Bypass: A Pilot Study |
title | Testing for Protein Leverage in Patients with Gastric Bypass: A Pilot Study |
title_full | Testing for Protein Leverage in Patients with Gastric Bypass: A Pilot Study |
title_fullStr | Testing for Protein Leverage in Patients with Gastric Bypass: A Pilot Study |
title_full_unstemmed | Testing for Protein Leverage in Patients with Gastric Bypass: A Pilot Study |
title_short | Testing for Protein Leverage in Patients with Gastric Bypass: A Pilot Study |
title_sort | testing for protein leverage in patients with gastric bypass: a pilot study |
topic | Human Nutrition: Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10614273/ https://www.ncbi.nlm.nih.gov/pubmed/37536296 http://dx.doi.org/10.1159/000532125 |
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