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The Malmö Offspring Study (MOS): design, methods and first results
As cardio metabolic disease manifestations tend to cluster in families there is a need to better understand the underlying mechanisms in order to further develop preventive strategies. In fact, genetic markers used in genetic risk scores, important as they are, will not be able alone to explain thes...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847466/ https://www.ncbi.nlm.nih.gov/pubmed/33222051 http://dx.doi.org/10.1007/s10654-020-00695-4 |
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author | Brunkwall, Louise Jönsson, Daniel Ericson, Ulrika Hellstrand, Sophie Kennbäck, Cecilia Östling, Gerd Jujic, Amra Melander, Olle Engström, Gunnar Nilsson, Jan Ohlsson, Bodil Klinge, Björn Orho-Melander, Marju Persson, Margaretha Nilsson, Peter M. |
author_facet | Brunkwall, Louise Jönsson, Daniel Ericson, Ulrika Hellstrand, Sophie Kennbäck, Cecilia Östling, Gerd Jujic, Amra Melander, Olle Engström, Gunnar Nilsson, Jan Ohlsson, Bodil Klinge, Björn Orho-Melander, Marju Persson, Margaretha Nilsson, Peter M. |
author_sort | Brunkwall, Louise |
collection | PubMed |
description | As cardio metabolic disease manifestations tend to cluster in families there is a need to better understand the underlying mechanisms in order to further develop preventive strategies. In fact, genetic markers used in genetic risk scores, important as they are, will not be able alone to explain these family clusters. Therefore, the search goes on for the so called missing heritability to better explain these associations. Shared lifestyle and social conditions in families, but also early life influences may be of importance. Gene-environmental interactions should be explored. In recent years interest has grown for the role of diet-microbiota associations, as microbiota patterns may be shared by family members. In the Malmö Offspring Study that started in 2013, we have so far been able to examine about 4700 subjects (18–71 years) representing children and grandchildren of index subjects from the first generation, examined in the Malmö Diet Cancer Study during 1991 to 1996. This will provide rich data and opportunities to analyse family traits of chronic disease across three generations. We will provide extensive genotyping and phenotyping including cardiovascular and respiratory function, as well as markers of glucose metabolism. In addition, also cognitive function will be assessed. A 4-day online dietary recall will be conducted and gut as well as oral microbiota analysed. The ambition is to provide one of the first large-scale European family studies with individual data across three generations, which could deepen our knowledge about the role of family traits for chronic disease and its underlying mechanisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10654-020-00695-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7847466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-78474662021-02-08 The Malmö Offspring Study (MOS): design, methods and first results Brunkwall, Louise Jönsson, Daniel Ericson, Ulrika Hellstrand, Sophie Kennbäck, Cecilia Östling, Gerd Jujic, Amra Melander, Olle Engström, Gunnar Nilsson, Jan Ohlsson, Bodil Klinge, Björn Orho-Melander, Marju Persson, Margaretha Nilsson, Peter M. Eur J Epidemiol New Study As cardio metabolic disease manifestations tend to cluster in families there is a need to better understand the underlying mechanisms in order to further develop preventive strategies. In fact, genetic markers used in genetic risk scores, important as they are, will not be able alone to explain these family clusters. Therefore, the search goes on for the so called missing heritability to better explain these associations. Shared lifestyle and social conditions in families, but also early life influences may be of importance. Gene-environmental interactions should be explored. In recent years interest has grown for the role of diet-microbiota associations, as microbiota patterns may be shared by family members. In the Malmö Offspring Study that started in 2013, we have so far been able to examine about 4700 subjects (18–71 years) representing children and grandchildren of index subjects from the first generation, examined in the Malmö Diet Cancer Study during 1991 to 1996. This will provide rich data and opportunities to analyse family traits of chronic disease across three generations. We will provide extensive genotyping and phenotyping including cardiovascular and respiratory function, as well as markers of glucose metabolism. In addition, also cognitive function will be assessed. A 4-day online dietary recall will be conducted and gut as well as oral microbiota analysed. The ambition is to provide one of the first large-scale European family studies with individual data across three generations, which could deepen our knowledge about the role of family traits for chronic disease and its underlying mechanisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10654-020-00695-4) contains supplementary material, which is available to authorized users. Springer Netherlands 2020-11-21 2021 /pmc/articles/PMC7847466/ /pubmed/33222051 http://dx.doi.org/10.1007/s10654-020-00695-4 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | New Study Brunkwall, Louise Jönsson, Daniel Ericson, Ulrika Hellstrand, Sophie Kennbäck, Cecilia Östling, Gerd Jujic, Amra Melander, Olle Engström, Gunnar Nilsson, Jan Ohlsson, Bodil Klinge, Björn Orho-Melander, Marju Persson, Margaretha Nilsson, Peter M. The Malmö Offspring Study (MOS): design, methods and first results |
title | The Malmö Offspring Study (MOS): design, methods and first results |
title_full | The Malmö Offspring Study (MOS): design, methods and first results |
title_fullStr | The Malmö Offspring Study (MOS): design, methods and first results |
title_full_unstemmed | The Malmö Offspring Study (MOS): design, methods and first results |
title_short | The Malmö Offspring Study (MOS): design, methods and first results |
title_sort | malmö offspring study (mos): design, methods and first results |
topic | New Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847466/ https://www.ncbi.nlm.nih.gov/pubmed/33222051 http://dx.doi.org/10.1007/s10654-020-00695-4 |
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