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Sex-associated differences in baseline urinary metabolites of healthy adults
The biological basis for gender variability among disease states is not well established. There have been many prior efforts attempting to identify the unique urine metabolomic profiles associated with specific diseases. However, there has been little advancement in investigating the metabolomic dif...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082868/ https://www.ncbi.nlm.nih.gov/pubmed/30089834 http://dx.doi.org/10.1038/s41598-018-29592-3 |
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author | Fan, Sili Yeon, Austin Shahid, Muhammad Anger, Jennifer T. Eilber, Karyn S. Fiehn, Oliver Kim, Jayoung |
author_facet | Fan, Sili Yeon, Austin Shahid, Muhammad Anger, Jennifer T. Eilber, Karyn S. Fiehn, Oliver Kim, Jayoung |
author_sort | Fan, Sili |
collection | PubMed |
description | The biological basis for gender variability among disease states is not well established. There have been many prior efforts attempting to identify the unique urine metabolomic profiles associated with specific diseases. However, there has been little advancement in investigating the metabolomic differences associated with gender, which underlies the misconception that risk factors and treatment regimens should be the same for both male and female patients. This present study aimed to identify biologically-meaningful baseline sex-related differences using urine samples provided by healthy female and male participants. To elucidate whether urinary metabolic signatures are globally distinct between healthy males and females, we applied metabolomics profiling of primary metabolism with comprehensive bioinformatics analyses on urine samples from 60 healthy males and females. We found that levels of α-ketoglutarate and 4-hydroxybutyric acid increased 2.3-fold and 4.41-fold in males compared to females, respectively. Furthermore, chemical similarity enrichment analysis revealed that differentially expressed metabolites, such as saturated fatty acids, TCA, and butyrates, were significantly related to the gender effect. These findings indicate that there are baseline sex-related differences in urinary metabolism, which should be considered in biomarker discovery, diagnosis, and treatment of bladder diseases, such as interstitial cystitis. |
format | Online Article Text |
id | pubmed-6082868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60828682018-08-10 Sex-associated differences in baseline urinary metabolites of healthy adults Fan, Sili Yeon, Austin Shahid, Muhammad Anger, Jennifer T. Eilber, Karyn S. Fiehn, Oliver Kim, Jayoung Sci Rep Article The biological basis for gender variability among disease states is not well established. There have been many prior efforts attempting to identify the unique urine metabolomic profiles associated with specific diseases. However, there has been little advancement in investigating the metabolomic differences associated with gender, which underlies the misconception that risk factors and treatment regimens should be the same for both male and female patients. This present study aimed to identify biologically-meaningful baseline sex-related differences using urine samples provided by healthy female and male participants. To elucidate whether urinary metabolic signatures are globally distinct between healthy males and females, we applied metabolomics profiling of primary metabolism with comprehensive bioinformatics analyses on urine samples from 60 healthy males and females. We found that levels of α-ketoglutarate and 4-hydroxybutyric acid increased 2.3-fold and 4.41-fold in males compared to females, respectively. Furthermore, chemical similarity enrichment analysis revealed that differentially expressed metabolites, such as saturated fatty acids, TCA, and butyrates, were significantly related to the gender effect. These findings indicate that there are baseline sex-related differences in urinary metabolism, which should be considered in biomarker discovery, diagnosis, and treatment of bladder diseases, such as interstitial cystitis. Nature Publishing Group UK 2018-08-08 /pmc/articles/PMC6082868/ /pubmed/30089834 http://dx.doi.org/10.1038/s41598-018-29592-3 Text en © The Author(s) 2018 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 Fan, Sili Yeon, Austin Shahid, Muhammad Anger, Jennifer T. Eilber, Karyn S. Fiehn, Oliver Kim, Jayoung Sex-associated differences in baseline urinary metabolites of healthy adults |
title | Sex-associated differences in baseline urinary metabolites of healthy adults |
title_full | Sex-associated differences in baseline urinary metabolites of healthy adults |
title_fullStr | Sex-associated differences in baseline urinary metabolites of healthy adults |
title_full_unstemmed | Sex-associated differences in baseline urinary metabolites of healthy adults |
title_short | Sex-associated differences in baseline urinary metabolites of healthy adults |
title_sort | sex-associated differences in baseline urinary metabolites of healthy adults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082868/ https://www.ncbi.nlm.nih.gov/pubmed/30089834 http://dx.doi.org/10.1038/s41598-018-29592-3 |
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