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Genetics of Severe Obesity

PURPOSE OF REVIEW: This review aims to present current information on genes underlying severe obesity, with the main emphasis on the three genes LEP, LEPR and MC4R. RECENT FINDINGS: There is a substantial amount of evidence that variants in at least ten different genes are the cause of severe monoge...

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Autores principales: Fairbrother, Una, Kidd, Elliot, Malagamuwa, Tanya, Walley, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105241/
https://www.ncbi.nlm.nih.gov/pubmed/30121879
http://dx.doi.org/10.1007/s11892-018-1053-x
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author Fairbrother, Una
Kidd, Elliot
Malagamuwa, Tanya
Walley, Andrew
author_facet Fairbrother, Una
Kidd, Elliot
Malagamuwa, Tanya
Walley, Andrew
author_sort Fairbrother, Una
collection PubMed
description PURPOSE OF REVIEW: This review aims to present current information on genes underlying severe obesity, with the main emphasis on the three genes LEP, LEPR and MC4R. RECENT FINDINGS: There is a substantial amount of evidence that variants in at least ten different genes are the cause of severe monogenic obesity. The majority of these are involved in the leptin-melanocortin signalling pathway. Due to the frequency of some of the identified variants, it is clear that monogenic variants also make a significant contribution to common obesity. SUMMARY: The artificial distinction between rare monogenic obesity and common polygenic obesity is now obsolete with the identification of MC4R variants of strong effect in the general population.
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spelling pubmed-61052412018-08-30 Genetics of Severe Obesity Fairbrother, Una Kidd, Elliot Malagamuwa, Tanya Walley, Andrew Curr Diab Rep Genetics (AP Morris, Section Editor) PURPOSE OF REVIEW: This review aims to present current information on genes underlying severe obesity, with the main emphasis on the three genes LEP, LEPR and MC4R. RECENT FINDINGS: There is a substantial amount of evidence that variants in at least ten different genes are the cause of severe monogenic obesity. The majority of these are involved in the leptin-melanocortin signalling pathway. Due to the frequency of some of the identified variants, it is clear that monogenic variants also make a significant contribution to common obesity. SUMMARY: The artificial distinction between rare monogenic obesity and common polygenic obesity is now obsolete with the identification of MC4R variants of strong effect in the general population. Springer US 2018-08-18 2018 /pmc/articles/PMC6105241/ /pubmed/30121879 http://dx.doi.org/10.1007/s11892-018-1053-x Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Genetics (AP Morris, Section Editor)
Fairbrother, Una
Kidd, Elliot
Malagamuwa, Tanya
Walley, Andrew
Genetics of Severe Obesity
title Genetics of Severe Obesity
title_full Genetics of Severe Obesity
title_fullStr Genetics of Severe Obesity
title_full_unstemmed Genetics of Severe Obesity
title_short Genetics of Severe Obesity
title_sort genetics of severe obesity
topic Genetics (AP Morris, Section Editor)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105241/
https://www.ncbi.nlm.nih.gov/pubmed/30121879
http://dx.doi.org/10.1007/s11892-018-1053-x
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