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Physiogenomic analysis of weight loss induced by dietary carbohydrate restriction

BACKGROUND: Diets that restrict carbohydrate (CHO) have proven to be a successful dietary treatment of obesity for many people, but the degree of weight loss varies across individuals. The extent to which genetic factors associate with the magnitude of weight loss induced by CHO restriction is unkno...

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Autores principales: Ruaño, Gualberto, Windemuth, Andreas, Kocherla, Mohan, Holford, Theodore, Fernandez, Maria Luz, Forsythe, Cassandra E, Wood, Richard J, Kraemer, William J, Volek, Jeff S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1479825/
https://www.ncbi.nlm.nih.gov/pubmed/16700901
http://dx.doi.org/10.1186/1743-7075-3-20
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author Ruaño, Gualberto
Windemuth, Andreas
Kocherla, Mohan
Holford, Theodore
Fernandez, Maria Luz
Forsythe, Cassandra E
Wood, Richard J
Kraemer, William J
Volek, Jeff S
author_facet Ruaño, Gualberto
Windemuth, Andreas
Kocherla, Mohan
Holford, Theodore
Fernandez, Maria Luz
Forsythe, Cassandra E
Wood, Richard J
Kraemer, William J
Volek, Jeff S
author_sort Ruaño, Gualberto
collection PubMed
description BACKGROUND: Diets that restrict carbohydrate (CHO) have proven to be a successful dietary treatment of obesity for many people, but the degree of weight loss varies across individuals. The extent to which genetic factors associate with the magnitude of weight loss induced by CHO restriction is unknown. We examined associations among polymorphisms in candidate genes and weight loss in order to understand the physiological factors influencing body weight responses to CHO restriction. METHODS: We screened for genetic associations with weight loss in 86 healthy adults who were instructed to restrict CHO to a level that induced a small level of ketosis (CHO ~10% of total energy). A total of 27 single nucleotide polymorphisms (SNPs) were selected from 15 candidate genes involved in fat digestion/metabolism, intracellular glucose metabolism, lipoprotein remodeling, and appetite regulation. Multiple linear regression was used to rank the SNPs according to probability of association, and the most significant associations were analyzed in greater detail. RESULTS: Mean weight loss was 6.4 kg. SNPs in the gastric lipase (LIPF), hepatic glycogen synthase (GYS2), cholesteryl ester transfer protein (CETP) and galanin (GAL) genes were significantly associated with weight loss. CONCLUSION: A strong association between weight loss induced by dietary CHO restriction and variability in genes regulating fat digestion, hepatic glucose metabolism, intravascular lipoprotein remodeling, and appetite were detected. These discoveries could provide clues to important physiologic adaptations underlying the body mass response to CHO restriction.
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spelling pubmed-14798252006-06-17 Physiogenomic analysis of weight loss induced by dietary carbohydrate restriction Ruaño, Gualberto Windemuth, Andreas Kocherla, Mohan Holford, Theodore Fernandez, Maria Luz Forsythe, Cassandra E Wood, Richard J Kraemer, William J Volek, Jeff S Nutr Metab (Lond) Research BACKGROUND: Diets that restrict carbohydrate (CHO) have proven to be a successful dietary treatment of obesity for many people, but the degree of weight loss varies across individuals. The extent to which genetic factors associate with the magnitude of weight loss induced by CHO restriction is unknown. We examined associations among polymorphisms in candidate genes and weight loss in order to understand the physiological factors influencing body weight responses to CHO restriction. METHODS: We screened for genetic associations with weight loss in 86 healthy adults who were instructed to restrict CHO to a level that induced a small level of ketosis (CHO ~10% of total energy). A total of 27 single nucleotide polymorphisms (SNPs) were selected from 15 candidate genes involved in fat digestion/metabolism, intracellular glucose metabolism, lipoprotein remodeling, and appetite regulation. Multiple linear regression was used to rank the SNPs according to probability of association, and the most significant associations were analyzed in greater detail. RESULTS: Mean weight loss was 6.4 kg. SNPs in the gastric lipase (LIPF), hepatic glycogen synthase (GYS2), cholesteryl ester transfer protein (CETP) and galanin (GAL) genes were significantly associated with weight loss. CONCLUSION: A strong association between weight loss induced by dietary CHO restriction and variability in genes regulating fat digestion, hepatic glucose metabolism, intravascular lipoprotein remodeling, and appetite were detected. These discoveries could provide clues to important physiologic adaptations underlying the body mass response to CHO restriction. BioMed Central 2006-05-15 /pmc/articles/PMC1479825/ /pubmed/16700901 http://dx.doi.org/10.1186/1743-7075-3-20 Text en Copyright © 2006 Ruaño et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Ruaño, Gualberto
Windemuth, Andreas
Kocherla, Mohan
Holford, Theodore
Fernandez, Maria Luz
Forsythe, Cassandra E
Wood, Richard J
Kraemer, William J
Volek, Jeff S
Physiogenomic analysis of weight loss induced by dietary carbohydrate restriction
title Physiogenomic analysis of weight loss induced by dietary carbohydrate restriction
title_full Physiogenomic analysis of weight loss induced by dietary carbohydrate restriction
title_fullStr Physiogenomic analysis of weight loss induced by dietary carbohydrate restriction
title_full_unstemmed Physiogenomic analysis of weight loss induced by dietary carbohydrate restriction
title_short Physiogenomic analysis of weight loss induced by dietary carbohydrate restriction
title_sort physiogenomic analysis of weight loss induced by dietary carbohydrate restriction
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1479825/
https://www.ncbi.nlm.nih.gov/pubmed/16700901
http://dx.doi.org/10.1186/1743-7075-3-20
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