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Role of UCP1 Gene Variants in Interethnic Differences in the Development of Cardio-Metabolic Diseases
Cardio-metabolic diseases (CMDs) comprise a cluster of risk factors that contribute to chronic pathological conditions with adverse consequences for cardiovascular function and metabolic processes. A wide range of CMD prevalence rates among different ethnic groups has been documented. In view of acc...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5277005/ https://www.ncbi.nlm.nih.gov/pubmed/28194159 http://dx.doi.org/10.3389/fgene.2017.00007 |
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author | Flouris, Andreas D. Shidlovskii, Yulii V. Shaposhnikov, Alexander V. Yepiskoposyan, Levon Nadolnik, Liliya Karabon, Lidia Kowalska, Anna Carrillo, Andres E. Metsios, George S. Sakellariou, Paraskevi |
author_facet | Flouris, Andreas D. Shidlovskii, Yulii V. Shaposhnikov, Alexander V. Yepiskoposyan, Levon Nadolnik, Liliya Karabon, Lidia Kowalska, Anna Carrillo, Andres E. Metsios, George S. Sakellariou, Paraskevi |
author_sort | Flouris, Andreas D. |
collection | PubMed |
description | Cardio-metabolic diseases (CMDs) comprise a cluster of risk factors that contribute to chronic pathological conditions with adverse consequences for cardiovascular function and metabolic processes. A wide range of CMD prevalence rates among different ethnic groups has been documented. In view of accumulated evidence, there is a trend toward increasing CMD prevalence rates in Eastern Europe and Western Asia. Numerous studies have revealed an association between uncoupling protein 1 (UCP1) gene variants and CMDs. UCP1 activity is essential for brown adipose tissue (BAT)-mediated thermogenesis. Experimental animal studies and epidemiological studies in humans highlight the significance of BAT-mediated thermogenesis in protecting against obesity and maintaining a lean phenotype. We hypothesize that the genetic variation in UCP1 gene expression observed among different ethnic groups could contribute to the ethnic-specific predisposition to CMD development. Constructing such prevalence maps of UCP1 gene variants could contribute significantly into identifying high-risk ethnic groups predisposed to the development of CMDs, and further shaping public health policies by the improvement of existing preventive and management strategies. |
format | Online Article Text |
id | pubmed-5277005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52770052017-02-13 Role of UCP1 Gene Variants in Interethnic Differences in the Development of Cardio-Metabolic Diseases Flouris, Andreas D. Shidlovskii, Yulii V. Shaposhnikov, Alexander V. Yepiskoposyan, Levon Nadolnik, Liliya Karabon, Lidia Kowalska, Anna Carrillo, Andres E. Metsios, George S. Sakellariou, Paraskevi Front Genet Genetics Cardio-metabolic diseases (CMDs) comprise a cluster of risk factors that contribute to chronic pathological conditions with adverse consequences for cardiovascular function and metabolic processes. A wide range of CMD prevalence rates among different ethnic groups has been documented. In view of accumulated evidence, there is a trend toward increasing CMD prevalence rates in Eastern Europe and Western Asia. Numerous studies have revealed an association between uncoupling protein 1 (UCP1) gene variants and CMDs. UCP1 activity is essential for brown adipose tissue (BAT)-mediated thermogenesis. Experimental animal studies and epidemiological studies in humans highlight the significance of BAT-mediated thermogenesis in protecting against obesity and maintaining a lean phenotype. We hypothesize that the genetic variation in UCP1 gene expression observed among different ethnic groups could contribute to the ethnic-specific predisposition to CMD development. Constructing such prevalence maps of UCP1 gene variants could contribute significantly into identifying high-risk ethnic groups predisposed to the development of CMDs, and further shaping public health policies by the improvement of existing preventive and management strategies. Frontiers Media S.A. 2017-01-30 /pmc/articles/PMC5277005/ /pubmed/28194159 http://dx.doi.org/10.3389/fgene.2017.00007 Text en Copyright © 2017 Flouris, Shidlovskii, Shaposhnikov, Yepiskoposyan, Nadolnik, Karabon, Kowalska, Carrillo, Metsios and Sakellariou. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Flouris, Andreas D. Shidlovskii, Yulii V. Shaposhnikov, Alexander V. Yepiskoposyan, Levon Nadolnik, Liliya Karabon, Lidia Kowalska, Anna Carrillo, Andres E. Metsios, George S. Sakellariou, Paraskevi Role of UCP1 Gene Variants in Interethnic Differences in the Development of Cardio-Metabolic Diseases |
title | Role of UCP1 Gene Variants in Interethnic Differences in the Development of Cardio-Metabolic Diseases |
title_full | Role of UCP1 Gene Variants in Interethnic Differences in the Development of Cardio-Metabolic Diseases |
title_fullStr | Role of UCP1 Gene Variants in Interethnic Differences in the Development of Cardio-Metabolic Diseases |
title_full_unstemmed | Role of UCP1 Gene Variants in Interethnic Differences in the Development of Cardio-Metabolic Diseases |
title_short | Role of UCP1 Gene Variants in Interethnic Differences in the Development of Cardio-Metabolic Diseases |
title_sort | role of ucp1 gene variants in interethnic differences in the development of cardio-metabolic diseases |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5277005/ https://www.ncbi.nlm.nih.gov/pubmed/28194159 http://dx.doi.org/10.3389/fgene.2017.00007 |
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