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Single nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases

BACKGROUND/OBJECTIVES: Obesity is an important risk factor for the development of diseases such as diabetes mellitus, hypertension, and dyslipidemia; however, a small number of individuals with long-standing obesity do not present with these cardiometabolic diseases. Such individuals are referred to...

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Autores principales: Schlauch, Karen A., Kulick, Doina, Subramanian, Krishnamurthy, De Meirleir, Kenny L., Palotás, András, Lombardi, Vincent C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365206/
https://www.ncbi.nlm.nih.gov/pubmed/30120429
http://dx.doi.org/10.1038/s41366-018-0181-3
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author Schlauch, Karen A.
Kulick, Doina
Subramanian, Krishnamurthy
De Meirleir, Kenny L.
Palotás, András
Lombardi, Vincent C.
author_facet Schlauch, Karen A.
Kulick, Doina
Subramanian, Krishnamurthy
De Meirleir, Kenny L.
Palotás, András
Lombardi, Vincent C.
author_sort Schlauch, Karen A.
collection PubMed
description BACKGROUND/OBJECTIVES: Obesity is an important risk factor for the development of diseases such as diabetes mellitus, hypertension, and dyslipidemia; however, a small number of individuals with long-standing obesity do not present with these cardiometabolic diseases. Such individuals are referred to as metabolically healthy obese (MHO) and potentially represent a subgroup of the general population with a protective genetic predisposition to obesity-related diseases. We hypothesized that individuals who were metabolically healthy but significantly obese (BMI ≥35 kg/m(2)) would represent a highly homogenous subgroup, with which to investigate potential genetic associations to obesity. We further hypothesized that such a cohort may lend itself well to investigate potential genotypes that are protective with respect to the development of cardiometabolic disease. SUBJECTS/METHODS: In the present study, we implemented this novel selection strategy by screening 892 individuals diagnosed as Class 2 or Class 3 obese and identified 38 who presented without any manifestations of cardiometabolic disease. We then assessed these subjects for single nucleotide polymorphisms (SNPs) that associated with this phenotype. RESULTS: Our analysis identified 89 SNPs that reach statistical significance (p<1×10(−5)), some of which are associated with genes of biological pathways that influences dietary behavior; others are associated with genes previously linked to obesity and cardiometabolic disease as well as neuroimmune disease. This study, to the best of our knowledge, represents the first genetic screening of a cardiometabolically healthy but significantly obese population.
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spelling pubmed-63652062019-02-17 Single nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases Schlauch, Karen A. Kulick, Doina Subramanian, Krishnamurthy De Meirleir, Kenny L. Palotás, András Lombardi, Vincent C. Int J Obes (Lond) Article BACKGROUND/OBJECTIVES: Obesity is an important risk factor for the development of diseases such as diabetes mellitus, hypertension, and dyslipidemia; however, a small number of individuals with long-standing obesity do not present with these cardiometabolic diseases. Such individuals are referred to as metabolically healthy obese (MHO) and potentially represent a subgroup of the general population with a protective genetic predisposition to obesity-related diseases. We hypothesized that individuals who were metabolically healthy but significantly obese (BMI ≥35 kg/m(2)) would represent a highly homogenous subgroup, with which to investigate potential genetic associations to obesity. We further hypothesized that such a cohort may lend itself well to investigate potential genotypes that are protective with respect to the development of cardiometabolic disease. SUBJECTS/METHODS: In the present study, we implemented this novel selection strategy by screening 892 individuals diagnosed as Class 2 or Class 3 obese and identified 38 who presented without any manifestations of cardiometabolic disease. We then assessed these subjects for single nucleotide polymorphisms (SNPs) that associated with this phenotype. RESULTS: Our analysis identified 89 SNPs that reach statistical significance (p<1×10(−5)), some of which are associated with genes of biological pathways that influences dietary behavior; others are associated with genes previously linked to obesity and cardiometabolic disease as well as neuroimmune disease. This study, to the best of our knowledge, represents the first genetic screening of a cardiometabolically healthy but significantly obese population. 2018-08-17 2019-02 /pmc/articles/PMC6365206/ /pubmed/30120429 http://dx.doi.org/10.1038/s41366-018-0181-3 Text en Users may view, print, copy, and download 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
Schlauch, Karen A.
Kulick, Doina
Subramanian, Krishnamurthy
De Meirleir, Kenny L.
Palotás, András
Lombardi, Vincent C.
Single nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases
title Single nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases
title_full Single nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases
title_fullStr Single nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases
title_full_unstemmed Single nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases
title_short Single nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases
title_sort single nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365206/
https://www.ncbi.nlm.nih.gov/pubmed/30120429
http://dx.doi.org/10.1038/s41366-018-0181-3
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