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Heritability and responses to high fat diet of plasma lipidomics in a twin study
Lipidomics have a great potential as clinical tool for monitoring metabolic changes in health and disease. Nevertheless hardly anything is known about the heritability of lipids. Therefore, it is necessary to clarify how and how much we can affect these progresses in individuals. In our intervention...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473837/ https://www.ncbi.nlm.nih.gov/pubmed/28623287 http://dx.doi.org/10.1038/s41598-017-03965-6 |
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author | Frahnow, Turid Osterhoff, Martin A. Hornemann, Silke Kruse, Michael Surma, Michal A. Klose, Christian Simons, Kai Pfeiffer, Andreas F. H. |
author_facet | Frahnow, Turid Osterhoff, Martin A. Hornemann, Silke Kruse, Michael Surma, Michal A. Klose, Christian Simons, Kai Pfeiffer, Andreas F. H. |
author_sort | Frahnow, Turid |
collection | PubMed |
description | Lipidomics have a great potential as clinical tool for monitoring metabolic changes in health and disease. Nevertheless hardly anything is known about the heritability of lipids. Therefore, it is necessary to clarify how and how much we can affect these progresses in individuals. In our interventional twin study (46 healthy, non-obese twin pairs) we investigated the lipid profile in plasma samples after switching from a low fat diet to an isocaloric high fat diet (HFD) to characterize the metabolic adaptation. Additionally we used the ACE model for Additive genetics, Common and unique Environment as well as linear mixed modelling to analyse the heritability of lipids. The heritability of lipids varied between 0–62% and applied to lipid species rather than to lipid classes. Phospholipids showed the highest inheritance. In addition, sex, body mass index (BMI) and age were important modifiers. The lipid profile changed already after one week of HFD and diverged further after 5 weeks of additional HFD. Basal concentrations of specific lipids within phospholipids are strongly inherited and are likely to be associated with heritable disease risks. BMI, sex and age were major modifiers. Nutrition strongly alters specific lipid classes, and has to be controlled in clinical association studies. |
format | Online Article Text |
id | pubmed-5473837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54738372017-06-21 Heritability and responses to high fat diet of plasma lipidomics in a twin study Frahnow, Turid Osterhoff, Martin A. Hornemann, Silke Kruse, Michael Surma, Michal A. Klose, Christian Simons, Kai Pfeiffer, Andreas F. H. Sci Rep Article Lipidomics have a great potential as clinical tool for monitoring metabolic changes in health and disease. Nevertheless hardly anything is known about the heritability of lipids. Therefore, it is necessary to clarify how and how much we can affect these progresses in individuals. In our interventional twin study (46 healthy, non-obese twin pairs) we investigated the lipid profile in plasma samples after switching from a low fat diet to an isocaloric high fat diet (HFD) to characterize the metabolic adaptation. Additionally we used the ACE model for Additive genetics, Common and unique Environment as well as linear mixed modelling to analyse the heritability of lipids. The heritability of lipids varied between 0–62% and applied to lipid species rather than to lipid classes. Phospholipids showed the highest inheritance. In addition, sex, body mass index (BMI) and age were important modifiers. The lipid profile changed already after one week of HFD and diverged further after 5 weeks of additional HFD. Basal concentrations of specific lipids within phospholipids are strongly inherited and are likely to be associated with heritable disease risks. BMI, sex and age were major modifiers. Nutrition strongly alters specific lipid classes, and has to be controlled in clinical association studies. Nature Publishing Group UK 2017-06-16 /pmc/articles/PMC5473837/ /pubmed/28623287 http://dx.doi.org/10.1038/s41598-017-03965-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Frahnow, Turid Osterhoff, Martin A. Hornemann, Silke Kruse, Michael Surma, Michal A. Klose, Christian Simons, Kai Pfeiffer, Andreas F. H. Heritability and responses to high fat diet of plasma lipidomics in a twin study |
title | Heritability and responses to high fat diet of plasma lipidomics in a twin study |
title_full | Heritability and responses to high fat diet of plasma lipidomics in a twin study |
title_fullStr | Heritability and responses to high fat diet of plasma lipidomics in a twin study |
title_full_unstemmed | Heritability and responses to high fat diet of plasma lipidomics in a twin study |
title_short | Heritability and responses to high fat diet of plasma lipidomics in a twin study |
title_sort | heritability and responses to high fat diet of plasma lipidomics in a twin study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473837/ https://www.ncbi.nlm.nih.gov/pubmed/28623287 http://dx.doi.org/10.1038/s41598-017-03965-6 |
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