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FTO predicts weight regain in the Look AHEAD Clinical Trial

BACKGROUND: Genome-wide association studies have provided new insights into the genetic factors that contribute to the development of obesity. We hypothesized that these genetic markers would also predict magnitude of weight loss and weight regain after initial weight loss. METHODS: Established obes...

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Autores principales: McCaffery, Jeanne, Papandonatos, George D., Huggins, Gordon S., Peter, Inga, Kahn, Steven E., Knowler, William C., Hudnall, Gina Evans, Lipkin, Edward, Kitabchi, Abbas E., Wagenknecht, Lynne E., Wing, Rena R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750057/
https://www.ncbi.nlm.nih.gov/pubmed/23628854
http://dx.doi.org/10.1038/ijo.2013.54
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author McCaffery, Jeanne
Papandonatos, George D.
Huggins, Gordon S.
Peter, Inga
Kahn, Steven E.
Knowler, William C.
Hudnall, Gina Evans
Lipkin, Edward
Kitabchi, Abbas E.
Wagenknecht, Lynne E.
Wing, Rena R.
author_facet McCaffery, Jeanne
Papandonatos, George D.
Huggins, Gordon S.
Peter, Inga
Kahn, Steven E.
Knowler, William C.
Hudnall, Gina Evans
Lipkin, Edward
Kitabchi, Abbas E.
Wagenknecht, Lynne E.
Wing, Rena R.
author_sort McCaffery, Jeanne
collection PubMed
description BACKGROUND: Genome-wide association studies have provided new insights into the genetic factors that contribute to the development of obesity. We hypothesized that these genetic markers would also predict magnitude of weight loss and weight regain after initial weight loss. METHODS: Established obesity risk alleles available on the Illumina CARe iSelect (IBC) chip were characterized in 3,899 overweight or obese participants with type 2 diabetes from the Look AHEAD (Action for Health in Diabetes), a randomized trial to determine the effects of intensive lifestyle intervention (ILI) and Diabetes Support and Education (DSE) on cardiovascular morbidity and mortality. Primary analyses examined the interaction between 13 obesity-risk polymorphisms in 8 genes and randomized treatment arm in predicting weight change at year 1, and weight regain at year 4 among individuals who lost 3% or more of their baseline weight by year 1. RESULTS: No SNPs were significantly associated with magnitude of weight loss or interacted with treatment arm at year 1. However, FTO rs3751812 predicted weight regain within DSE (1.56 kg per risk allele, p = 0.005), but not ILI (p = 0.761), resulting in SNP×treatment arm interaction (p = 0.009). In a partial replication of prior research, the obesity risk (G) allele at BDNF rs6265 was associated with greater weight regain across treatment arms (0.773 kg per risk allele), although results were of borderline statistical significance (p=0.051). CONCLUSIONS: Variations in the FTO and BDNF loci may contribute risk of weight regain after weight loss.
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spelling pubmed-37500572014-06-01 FTO predicts weight regain in the Look AHEAD Clinical Trial McCaffery, Jeanne Papandonatos, George D. Huggins, Gordon S. Peter, Inga Kahn, Steven E. Knowler, William C. Hudnall, Gina Evans Lipkin, Edward Kitabchi, Abbas E. Wagenknecht, Lynne E. Wing, Rena R. Int J Obes (Lond) Article BACKGROUND: Genome-wide association studies have provided new insights into the genetic factors that contribute to the development of obesity. We hypothesized that these genetic markers would also predict magnitude of weight loss and weight regain after initial weight loss. METHODS: Established obesity risk alleles available on the Illumina CARe iSelect (IBC) chip were characterized in 3,899 overweight or obese participants with type 2 diabetes from the Look AHEAD (Action for Health in Diabetes), a randomized trial to determine the effects of intensive lifestyle intervention (ILI) and Diabetes Support and Education (DSE) on cardiovascular morbidity and mortality. Primary analyses examined the interaction between 13 obesity-risk polymorphisms in 8 genes and randomized treatment arm in predicting weight change at year 1, and weight regain at year 4 among individuals who lost 3% or more of their baseline weight by year 1. RESULTS: No SNPs were significantly associated with magnitude of weight loss or interacted with treatment arm at year 1. However, FTO rs3751812 predicted weight regain within DSE (1.56 kg per risk allele, p = 0.005), but not ILI (p = 0.761), resulting in SNP×treatment arm interaction (p = 0.009). In a partial replication of prior research, the obesity risk (G) allele at BDNF rs6265 was associated with greater weight regain across treatment arms (0.773 kg per risk allele), although results were of borderline statistical significance (p=0.051). CONCLUSIONS: Variations in the FTO and BDNF loci may contribute risk of weight regain after weight loss. 2013-04-03 2013-12 /pmc/articles/PMC3750057/ /pubmed/23628854 http://dx.doi.org/10.1038/ijo.2013.54 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
McCaffery, Jeanne
Papandonatos, George D.
Huggins, Gordon S.
Peter, Inga
Kahn, Steven E.
Knowler, William C.
Hudnall, Gina Evans
Lipkin, Edward
Kitabchi, Abbas E.
Wagenknecht, Lynne E.
Wing, Rena R.
FTO predicts weight regain in the Look AHEAD Clinical Trial
title FTO predicts weight regain in the Look AHEAD Clinical Trial
title_full FTO predicts weight regain in the Look AHEAD Clinical Trial
title_fullStr FTO predicts weight regain in the Look AHEAD Clinical Trial
title_full_unstemmed FTO predicts weight regain in the Look AHEAD Clinical Trial
title_short FTO predicts weight regain in the Look AHEAD Clinical Trial
title_sort fto predicts weight regain in the look ahead clinical trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750057/
https://www.ncbi.nlm.nih.gov/pubmed/23628854
http://dx.doi.org/10.1038/ijo.2013.54
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