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Lipidomic analysis of plasma samples from women with polycystic ovary syndrome
Polycystic ovary syndrome (PCOS) is a common disorder affecting between 5 and 18 % of females of reproductive age and can be diagnosed based on a combination of clinical, ultrasound and biochemical features, none of which on its own is diagnostic. A lipidomic approach using liquid chromatography cou...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419155/ https://www.ncbi.nlm.nih.gov/pubmed/25972770 http://dx.doi.org/10.1007/s11306-014-0726-y |
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author | Haoula, Zeina Ravipati, Srinivasarao Stekel, Dov J. Ortori, Catharine A. Hodgman, Charlie Daykin, Clare Raine-Fenning, Nick Barrett, David A. Atiomo, William |
author_facet | Haoula, Zeina Ravipati, Srinivasarao Stekel, Dov J. Ortori, Catharine A. Hodgman, Charlie Daykin, Clare Raine-Fenning, Nick Barrett, David A. Atiomo, William |
author_sort | Haoula, Zeina |
collection | PubMed |
description | Polycystic ovary syndrome (PCOS) is a common disorder affecting between 5 and 18 % of females of reproductive age and can be diagnosed based on a combination of clinical, ultrasound and biochemical features, none of which on its own is diagnostic. A lipidomic approach using liquid chromatography coupled with accurate mass high-resolution mass-spectrometry (LC-HRMS) was used to investigate if there were any differences in plasma lipidomic profiles in women with PCOS compared with control women at different stages of menstrual cycle. Plasma samples from 40 women with PCOS and 40 controls aged between 18 and 40 years were analysed in combination with multivariate statistical analyses. Multivariate data analysis (LASSO regression and OPLS-DA) of the sample lipidomics datasets showed a weak prediction model for PCOS versus control samples from the follicular and mid-cycle phases of the menstrual cycle, but a stronger model (specificity 85 % and sensitivity 95 %) for PCOS versus the luteal phase menstrual cycle controls. The PCOS vs luteal phase model showed increased levels of plasma triglycerides and sphingomyelins and decreased levels of lysophosphatidylcholines and phosphatidylethanolamines in PCOS women compared with controls. Lipid biomarkers of PCOS were tentatively identified which may be useful in distinguishing PCOS from controls especially when performed during the menstrual cycle luteal phase. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11306-014-0726-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4419155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-44191552015-05-11 Lipidomic analysis of plasma samples from women with polycystic ovary syndrome Haoula, Zeina Ravipati, Srinivasarao Stekel, Dov J. Ortori, Catharine A. Hodgman, Charlie Daykin, Clare Raine-Fenning, Nick Barrett, David A. Atiomo, William Metabolomics Original Article Polycystic ovary syndrome (PCOS) is a common disorder affecting between 5 and 18 % of females of reproductive age and can be diagnosed based on a combination of clinical, ultrasound and biochemical features, none of which on its own is diagnostic. A lipidomic approach using liquid chromatography coupled with accurate mass high-resolution mass-spectrometry (LC-HRMS) was used to investigate if there were any differences in plasma lipidomic profiles in women with PCOS compared with control women at different stages of menstrual cycle. Plasma samples from 40 women with PCOS and 40 controls aged between 18 and 40 years were analysed in combination with multivariate statistical analyses. Multivariate data analysis (LASSO regression and OPLS-DA) of the sample lipidomics datasets showed a weak prediction model for PCOS versus control samples from the follicular and mid-cycle phases of the menstrual cycle, but a stronger model (specificity 85 % and sensitivity 95 %) for PCOS versus the luteal phase menstrual cycle controls. The PCOS vs luteal phase model showed increased levels of plasma triglycerides and sphingomyelins and decreased levels of lysophosphatidylcholines and phosphatidylethanolamines in PCOS women compared with controls. Lipid biomarkers of PCOS were tentatively identified which may be useful in distinguishing PCOS from controls especially when performed during the menstrual cycle luteal phase. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11306-014-0726-y) contains supplementary material, which is available to authorized users. Springer US 2014-08-17 2015 /pmc/articles/PMC4419155/ /pubmed/25972770 http://dx.doi.org/10.1007/s11306-014-0726-y Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Haoula, Zeina Ravipati, Srinivasarao Stekel, Dov J. Ortori, Catharine A. Hodgman, Charlie Daykin, Clare Raine-Fenning, Nick Barrett, David A. Atiomo, William Lipidomic analysis of plasma samples from women with polycystic ovary syndrome |
title | Lipidomic analysis of plasma samples from women with polycystic ovary syndrome |
title_full | Lipidomic analysis of plasma samples from women with polycystic ovary syndrome |
title_fullStr | Lipidomic analysis of plasma samples from women with polycystic ovary syndrome |
title_full_unstemmed | Lipidomic analysis of plasma samples from women with polycystic ovary syndrome |
title_short | Lipidomic analysis of plasma samples from women with polycystic ovary syndrome |
title_sort | lipidomic analysis of plasma samples from women with polycystic ovary syndrome |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419155/ https://www.ncbi.nlm.nih.gov/pubmed/25972770 http://dx.doi.org/10.1007/s11306-014-0726-y |
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