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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.
Affiliation
  • Varga TV; Novo Nordisk Foundation Center for Protein Research, Translational Disease Systems Biology Group, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Ali A; Department of Clinical Sciences, Genetic and Molecular Epidemiology Unit, Lund University, Skåne University Hospital Malmö, Malmö, Sweden.
  • Herrera JAR; Steno Diabetes Center Copenhagen, Gentofte, Denmark.
  • Ahonen LL; National Bioinformatics Infrastructure Sweden (NBIS), SciLifeLab, Lund, Sweden.
  • Mattila IM; Novo Nordisk Foundation Center for Protein Research, Translational Disease Systems Biology Group, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Al-Sari NH; Steno Diabetes Center Copenhagen, Gentofte, Denmark.
  • Legido-Quigley C; Biosyntia ApS, Copenhagen, Denmark.
  • Skouby S; Steno Diabetes Center Copenhagen, Gentofte, Denmark.
  • Brunak S; Steno Diabetes Center Copenhagen, Gentofte, Denmark.
  • Tornberg ÅB; Steno Diabetes Center Copenhagen, Gentofte, Denmark.
Sci Rep ; 10(1): 2349, 2020 02 11.
Article in En | MEDLINE | ID: mdl-32047202
ABSTRACT
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 PFDR < 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 (PFisher = 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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Physical Endurance / Biomarkers / Exercise / Athletes / Lipidomics / Lipids Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Female / Humans Language: En Journal: Sci Rep Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Physical Endurance / Biomarkers / Exercise / Athletes / Lipidomics / Lipids Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Female / Humans Language: En Journal: Sci Rep Year: 2020 Document type: Article Affiliation country: