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Lipidomic profiles, lipid trajectories and clinical biomarkers in female elite endurance athletes
We assessed whether blood lipid metabolites and their changes associate with various cardiometabolic, endocrine, bone- and energy-related comorbidities of Relative Energy Deficiency in Sport (RED-S) in female elite endurance athletes. Thirty-eight Scandinavian female elite athletes underwent a day-l...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012926/ https://www.ncbi.nlm.nih.gov/pubmed/32047202 http://dx.doi.org/10.1038/s41598-020-59127-8 |
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author | Varga, Tibor V. Ali, Ashfaq Herrera, Jose A. R. Ahonen, Linda L. Mattila, Ismo M. Al-Sari, Naba H. Legido-Quigley, Cristina Skouby, Sven Brunak, Søren Tornberg, Åsa B. |
author_facet | Varga, Tibor V. Ali, Ashfaq Herrera, Jose A. R. Ahonen, Linda L. Mattila, Ismo M. Al-Sari, Naba H. Legido-Quigley, Cristina Skouby, Sven Brunak, Søren Tornberg, Åsa B. |
author_sort | Varga, Tibor V. |
collection | PubMed |
description | We assessed whether blood lipid metabolites and their changes associate with various cardiometabolic, endocrine, bone- and energy-related comorbidities of Relative Energy Deficiency in Sport (RED-S) in female elite endurance athletes. Thirty-eight Scandinavian female elite athletes underwent a day-long exercise test. Five blood samples were obtained during the day - at fasting state and before and after two standardized exercise tests. Clinical biomarkers were assessed at fasting state, while untargeted lipidomics was undertaken using all blood samples. Linear and logistic regression was used to assess associations between lipidomic features and clinical biomarkers. Overrepresentations of findings with P < 0.05 from these association tests were assessed using Fisher’s exact tests. Self-organizing maps and a trajectory clustering algorithm were utilized to identify informative clusters in the population. Twenty associations P(FDR) < 0.05 were detected between lipidomic features and clinical biomarkers. Notably, cortisol demonstrated an overrepresentation of associations with P < 0.05 compared to other traits (P(Fisher) = 1.9×10(−14)). Mean lipid trajectories were created for 201 named features for the cohort and subsequently by stratifying participants by their energy availability and menstrual dysfunction status. This exploratory analysis of lipid trajectories indicates that participants with menstrual dysfunction might have decreased adaptive response to exercise interventions. |
format | Online Article Text |
id | pubmed-7012926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70129262020-02-21 Lipidomic profiles, lipid trajectories and clinical biomarkers in female elite endurance athletes Varga, Tibor V. Ali, Ashfaq Herrera, Jose A. R. Ahonen, Linda L. Mattila, Ismo M. Al-Sari, Naba H. Legido-Quigley, Cristina Skouby, Sven Brunak, Søren Tornberg, Åsa B. Sci Rep Article We assessed whether blood lipid metabolites and their changes associate with various cardiometabolic, endocrine, bone- and energy-related comorbidities of Relative Energy Deficiency in Sport (RED-S) in female elite endurance athletes. Thirty-eight Scandinavian female elite athletes underwent a day-long exercise test. Five blood samples were obtained during the day - at fasting state and before and after two standardized exercise tests. Clinical biomarkers were assessed at fasting state, while untargeted lipidomics was undertaken using all blood samples. Linear and logistic regression was used to assess associations between lipidomic features and clinical biomarkers. Overrepresentations of findings with P < 0.05 from these association tests were assessed using Fisher’s exact tests. Self-organizing maps and a trajectory clustering algorithm were utilized to identify informative clusters in the population. Twenty associations P(FDR) < 0.05 were detected between lipidomic features and clinical biomarkers. Notably, cortisol demonstrated an overrepresentation of associations with P < 0.05 compared to other traits (P(Fisher) = 1.9×10(−14)). Mean lipid trajectories were created for 201 named features for the cohort and subsequently by stratifying participants by their energy availability and menstrual dysfunction status. This exploratory analysis of lipid trajectories indicates that participants with menstrual dysfunction might have decreased adaptive response to exercise interventions. Nature Publishing Group UK 2020-02-11 /pmc/articles/PMC7012926/ /pubmed/32047202 http://dx.doi.org/10.1038/s41598-020-59127-8 Text en © The Author(s) 2020 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 Varga, Tibor V. Ali, Ashfaq Herrera, Jose A. R. Ahonen, Linda L. Mattila, Ismo M. Al-Sari, Naba H. Legido-Quigley, Cristina Skouby, Sven Brunak, Søren Tornberg, Åsa B. Lipidomic profiles, lipid trajectories and clinical biomarkers in female elite endurance athletes |
title | Lipidomic profiles, lipid trajectories and clinical biomarkers in female elite endurance athletes |
title_full | Lipidomic profiles, lipid trajectories and clinical biomarkers in female elite endurance athletes |
title_fullStr | Lipidomic profiles, lipid trajectories and clinical biomarkers in female elite endurance athletes |
title_full_unstemmed | Lipidomic profiles, lipid trajectories and clinical biomarkers in female elite endurance athletes |
title_short | Lipidomic profiles, lipid trajectories and clinical biomarkers in female elite endurance athletes |
title_sort | lipidomic profiles, lipid trajectories and clinical biomarkers in female elite endurance athletes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012926/ https://www.ncbi.nlm.nih.gov/pubmed/32047202 http://dx.doi.org/10.1038/s41598-020-59127-8 |
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