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Modulation of the lipidomic profile due to a lipid challenge and fitness level: a postprandial study

BACKGROUND: The lipid composition of plasma is known to vary due to both phenotypic factors such as age, gender and BMI as well as with various diseases including cancer and neurological disorders. However, there is little investigation into the variation in the lipidome due to exercise and/ or meta...

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Autores principales: Morris, Ciara, O’Grada, Colm M., Ryan, Miriam F., Gibney, Michael J., Roche, Helen M., Gibney, Eileen R., Brennan, Lorraine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489019/
https://www.ncbi.nlm.nih.gov/pubmed/26123789
http://dx.doi.org/10.1186/s12944-015-0062-x
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author Morris, Ciara
O’Grada, Colm M.
Ryan, Miriam F.
Gibney, Michael J.
Roche, Helen M.
Gibney, Eileen R.
Brennan, Lorraine
author_facet Morris, Ciara
O’Grada, Colm M.
Ryan, Miriam F.
Gibney, Michael J.
Roche, Helen M.
Gibney, Eileen R.
Brennan, Lorraine
author_sort Morris, Ciara
collection PubMed
description BACKGROUND: The lipid composition of plasma is known to vary due to both phenotypic factors such as age, gender and BMI as well as with various diseases including cancer and neurological disorders. However, there is little investigation into the variation in the lipidome due to exercise and/ or metabolic challenges. The objectives of this present study were (i) To identify the glycerophospholipid, sphingolipids and ceramide changes in response to an oral lipid tolerance test (OLTT) in healthy adults and (ii) To identify the effect of aerobic fitness level on lipidomic profiles. METHODS: 214 healthy adults aged 18–60 years were recruited as part of a metabolic challenge study. A sub-group of 40 volunteers were selected for lipidomic analysis based on their aerobic fitness level. Ceramides, glycerophospholipids and sphingomyelins were quantified in baseline fasting plasma samples as well as at 60, 120, 180, 240 and 300 min following a lipid challenge using high-throughput flow injection ESI-MS/MS. RESULTS: Mixed model repeated measures analysis identified lipids which were significantly changing over the time course of the lipid challenge. Included in these lipids were lysophosphoethanolamines (LPE), phosphoethanolamines (PE), phosphoglycerides (PG) and ceramides (Cer). Five lipids (LPE a C18:2, LPE a C18:1, PE aa C36:2, PE aa C36:3 and N-C16:1-Cer) had a fold change > 1.5 at 120 min following the challenge and these lipids remained elevated. Furthermore, three of these lipids (LPE a C18:2, PE aa C36:2 and PE aa C36:3) were predictive of fasting and peak plasma TAG concentrations following the OLTT. Further analysis revealed that fitness level has a significant impact on the response to the OLTT: in particular significant differences between fitness groups were observed for phosphatidylcholines (PC), sphingomyelins (SM) and ceramides. CONCLUSION: This study identified specific lipids which were modulated by an acute lipid challenge. Furthermore, it identified a series of lipids which were modulated by fitness level. Future lipidomic studies should take into account environmental factors such as diet and fitness level during biomarker discovery work. TRIAL REGISTRATION: Data, clinicaltrials.gov, NCT01172951 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12944-015-0062-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-44890192015-07-03 Modulation of the lipidomic profile due to a lipid challenge and fitness level: a postprandial study Morris, Ciara O’Grada, Colm M. Ryan, Miriam F. Gibney, Michael J. Roche, Helen M. Gibney, Eileen R. Brennan, Lorraine Lipids Health Dis Research BACKGROUND: The lipid composition of plasma is known to vary due to both phenotypic factors such as age, gender and BMI as well as with various diseases including cancer and neurological disorders. However, there is little investigation into the variation in the lipidome due to exercise and/ or metabolic challenges. The objectives of this present study were (i) To identify the glycerophospholipid, sphingolipids and ceramide changes in response to an oral lipid tolerance test (OLTT) in healthy adults and (ii) To identify the effect of aerobic fitness level on lipidomic profiles. METHODS: 214 healthy adults aged 18–60 years were recruited as part of a metabolic challenge study. A sub-group of 40 volunteers were selected for lipidomic analysis based on their aerobic fitness level. Ceramides, glycerophospholipids and sphingomyelins were quantified in baseline fasting plasma samples as well as at 60, 120, 180, 240 and 300 min following a lipid challenge using high-throughput flow injection ESI-MS/MS. RESULTS: Mixed model repeated measures analysis identified lipids which were significantly changing over the time course of the lipid challenge. Included in these lipids were lysophosphoethanolamines (LPE), phosphoethanolamines (PE), phosphoglycerides (PG) and ceramides (Cer). Five lipids (LPE a C18:2, LPE a C18:1, PE aa C36:2, PE aa C36:3 and N-C16:1-Cer) had a fold change > 1.5 at 120 min following the challenge and these lipids remained elevated. Furthermore, three of these lipids (LPE a C18:2, PE aa C36:2 and PE aa C36:3) were predictive of fasting and peak plasma TAG concentrations following the OLTT. Further analysis revealed that fitness level has a significant impact on the response to the OLTT: in particular significant differences between fitness groups were observed for phosphatidylcholines (PC), sphingomyelins (SM) and ceramides. CONCLUSION: This study identified specific lipids which were modulated by an acute lipid challenge. Furthermore, it identified a series of lipids which were modulated by fitness level. Future lipidomic studies should take into account environmental factors such as diet and fitness level during biomarker discovery work. TRIAL REGISTRATION: Data, clinicaltrials.gov, NCT01172951 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12944-015-0062-x) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-01 /pmc/articles/PMC4489019/ /pubmed/26123789 http://dx.doi.org/10.1186/s12944-015-0062-x Text en © Morris et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Morris, Ciara
O’Grada, Colm M.
Ryan, Miriam F.
Gibney, Michael J.
Roche, Helen M.
Gibney, Eileen R.
Brennan, Lorraine
Modulation of the lipidomic profile due to a lipid challenge and fitness level: a postprandial study
title Modulation of the lipidomic profile due to a lipid challenge and fitness level: a postprandial study
title_full Modulation of the lipidomic profile due to a lipid challenge and fitness level: a postprandial study
title_fullStr Modulation of the lipidomic profile due to a lipid challenge and fitness level: a postprandial study
title_full_unstemmed Modulation of the lipidomic profile due to a lipid challenge and fitness level: a postprandial study
title_short Modulation of the lipidomic profile due to a lipid challenge and fitness level: a postprandial study
title_sort modulation of the lipidomic profile due to a lipid challenge and fitness level: a postprandial study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489019/
https://www.ncbi.nlm.nih.gov/pubmed/26123789
http://dx.doi.org/10.1186/s12944-015-0062-x
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