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Molecular Sex Differences in Human Serum

BACKGROUND: Sex is an important factor in the prevalence, incidence, progression, and response to treatment of many medical conditions, including autoimmune and cardiovascular diseases and psychiatric conditions. Identification of molecular differences between typical males and females can provide a...

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Autores principales: Ramsey, Jordan M., Schwarz, Emanuel, Guest, Paul C., van Beveren, Nico J. M., Leweke, F. Markus, Rothermundt, Matthias, Bogerts, Bernhard, Steiner, Johann, Ruta, Liliana, Baron-Cohen, Simon, Bahn, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520798/
https://www.ncbi.nlm.nih.gov/pubmed/23251558
http://dx.doi.org/10.1371/journal.pone.0051504
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author Ramsey, Jordan M.
Schwarz, Emanuel
Guest, Paul C.
van Beveren, Nico J. M.
Leweke, F. Markus
Rothermundt, Matthias
Bogerts, Bernhard
Steiner, Johann
Ruta, Liliana
Baron-Cohen, Simon
Bahn, Sabine
author_facet Ramsey, Jordan M.
Schwarz, Emanuel
Guest, Paul C.
van Beveren, Nico J. M.
Leweke, F. Markus
Rothermundt, Matthias
Bogerts, Bernhard
Steiner, Johann
Ruta, Liliana
Baron-Cohen, Simon
Bahn, Sabine
author_sort Ramsey, Jordan M.
collection PubMed
description BACKGROUND: Sex is an important factor in the prevalence, incidence, progression, and response to treatment of many medical conditions, including autoimmune and cardiovascular diseases and psychiatric conditions. Identification of molecular differences between typical males and females can provide a valuable basis for exploring conditions differentially affected by sex. METHODOLOGY/PRINCIPAL FINDINGS: Using multiplexed immunoassays, we analyzed 174 serum molecules in 9 independent cohorts of typical individuals, comprising 196 males and 196 females. Sex differences in analyte levels were quantified using a meta-analysis approach and put into biological context using k-means to generate clusters of analytes with distinct biological functions. Natural sex differences were established in these analyte groups and these were applied to illustrate sexually dimorphic analyte expression in a cohort of 22 males and 22 females with Asperger syndrome. Reproducible sex differences were found in the levels of 77 analytes in serum of typical controls, and these comprised clusters of molecules enriched with distinct biological functions. Analytes involved in fatty acid oxidation/hormone regulation, immune cell growth and activation, and cell death were found at higher levels in females, and analytes involved in immune cell chemotaxis and other indistinct functions were higher in males. Comparison of these naturally occurring sex differences against a cohort of people with Asperger syndrome indicated that a cluster of analytes that had functions related to fatty acid oxidation/hormone regulation was associated with sex and the occurrence of this condition. CONCLUSIONS/SIGNIFICANCE: Sex-specific molecular differences were detected in serum of typical controls and these were reproducible across independent cohorts. This study extends current knowledge of sex differences in biological functions involved in metabolism and immune function. Deviations from typical sex differences were found in a cluster of molecules in Asperger syndrome. These findings illustrate the importance of investigating the influence of sex on medical conditions.
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spelling pubmed-35207982012-12-18 Molecular Sex Differences in Human Serum Ramsey, Jordan M. Schwarz, Emanuel Guest, Paul C. van Beveren, Nico J. M. Leweke, F. Markus Rothermundt, Matthias Bogerts, Bernhard Steiner, Johann Ruta, Liliana Baron-Cohen, Simon Bahn, Sabine PLoS One Research Article BACKGROUND: Sex is an important factor in the prevalence, incidence, progression, and response to treatment of many medical conditions, including autoimmune and cardiovascular diseases and psychiatric conditions. Identification of molecular differences between typical males and females can provide a valuable basis for exploring conditions differentially affected by sex. METHODOLOGY/PRINCIPAL FINDINGS: Using multiplexed immunoassays, we analyzed 174 serum molecules in 9 independent cohorts of typical individuals, comprising 196 males and 196 females. Sex differences in analyte levels were quantified using a meta-analysis approach and put into biological context using k-means to generate clusters of analytes with distinct biological functions. Natural sex differences were established in these analyte groups and these were applied to illustrate sexually dimorphic analyte expression in a cohort of 22 males and 22 females with Asperger syndrome. Reproducible sex differences were found in the levels of 77 analytes in serum of typical controls, and these comprised clusters of molecules enriched with distinct biological functions. Analytes involved in fatty acid oxidation/hormone regulation, immune cell growth and activation, and cell death were found at higher levels in females, and analytes involved in immune cell chemotaxis and other indistinct functions were higher in males. Comparison of these naturally occurring sex differences against a cohort of people with Asperger syndrome indicated that a cluster of analytes that had functions related to fatty acid oxidation/hormone regulation was associated with sex and the occurrence of this condition. CONCLUSIONS/SIGNIFICANCE: Sex-specific molecular differences were detected in serum of typical controls and these were reproducible across independent cohorts. This study extends current knowledge of sex differences in biological functions involved in metabolism and immune function. Deviations from typical sex differences were found in a cluster of molecules in Asperger syndrome. These findings illustrate the importance of investigating the influence of sex on medical conditions. Public Library of Science 2012-12-12 /pmc/articles/PMC3520798/ /pubmed/23251558 http://dx.doi.org/10.1371/journal.pone.0051504 Text en © 2012 Ramsey et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ramsey, Jordan M.
Schwarz, Emanuel
Guest, Paul C.
van Beveren, Nico J. M.
Leweke, F. Markus
Rothermundt, Matthias
Bogerts, Bernhard
Steiner, Johann
Ruta, Liliana
Baron-Cohen, Simon
Bahn, Sabine
Molecular Sex Differences in Human Serum
title Molecular Sex Differences in Human Serum
title_full Molecular Sex Differences in Human Serum
title_fullStr Molecular Sex Differences in Human Serum
title_full_unstemmed Molecular Sex Differences in Human Serum
title_short Molecular Sex Differences in Human Serum
title_sort molecular sex differences in human serum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520798/
https://www.ncbi.nlm.nih.gov/pubmed/23251558
http://dx.doi.org/10.1371/journal.pone.0051504
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