Metabolomic differences between critically Ill women and men

Abstract Metabolism differs in women and men at homeostasis. Critically ill patients have profound dysregulation of homeostasis and metabolism. It is not clear if the metabolic response to critical illness differs in women compared to men. Such sex-specific differences in illness response would have...

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Main Authors: Sowmya Chary, Karin Amrein, Jessica A. Lasky-Su, Harald Dobnig, Kenneth B. Christopher
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-83602-5
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spelling doaj-08901062dd8d4176b2c1e7b834afaf462021-02-21T12:31:11ZengNature Publishing GroupScientific Reports2045-23222021-02-0111111110.1038/s41598-021-83602-5Metabolomic differences between critically Ill women and menSowmya Chary0Karin Amrein1Jessica A. Lasky-Su2Harald Dobnig3Kenneth B. Christopher4Biogen, Inc.Division of Endocrinology and Diabetology, Medical University of GrazChanning Division of Network Medicine, Brigham and Women’s HospitalThyroid Endocrinology Osteoporosis Institute DobnigChanning Division of Network Medicine, Brigham and Women’s HospitalAbstract Metabolism differs in women and men at homeostasis. Critically ill patients have profound dysregulation of homeostasis and metabolism. It is not clear if the metabolic response to critical illness differs in women compared to men. Such sex-specific differences in illness response would have consequences for personalized medicine. Our aim was to determine the sex-specific metabolomic response to early critical illness. We performed a post-hoc metabolomics study of the VITdAL-ICU trial where subjects received high dose vitamin D3 or placebo. Using mixed-effects modeling, we studied sex-specific changes in metabolites over time adjusted for age, Simplified Acute Physiology Score II, admission diagnosis, day 0 25-hydroxyvitamin D level, and 25-hydroxyvitamin D response to intervention. In women, multiple members of the sphingomyelin and lysophospholipid metabolite classes had significantly positive Bonferroni corrected associations over time compared to men. Further, multiple representatives of the acylcarnitine, androgenic steroid, bile acid, nucleotide and amino acid metabolite classes had significantly negative Bonferroni corrected associations over time compared to men. Gaussian graphical model analyses revealed sex-specific functional modules. Our findings show that robust and coordinated sex-specific metabolite differences exist early in critical illness.https://doi.org/10.1038/s41598-021-83602-5
collection DOAJ
language English
format Article
sources DOAJ
author Sowmya Chary
Karin Amrein
Jessica A. Lasky-Su
Harald Dobnig
Kenneth B. Christopher
spellingShingle Sowmya Chary
Karin Amrein
Jessica A. Lasky-Su
Harald Dobnig
Kenneth B. Christopher
Metabolomic differences between critically Ill women and men
Scientific Reports
author_facet Sowmya Chary
Karin Amrein
Jessica A. Lasky-Su
Harald Dobnig
Kenneth B. Christopher
author_sort Sowmya Chary
title Metabolomic differences between critically Ill women and men
title_short Metabolomic differences between critically Ill women and men
title_full Metabolomic differences between critically Ill women and men
title_fullStr Metabolomic differences between critically Ill women and men
title_full_unstemmed Metabolomic differences between critically Ill women and men
title_sort metabolomic differences between critically ill women and men
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-02-01
description Abstract Metabolism differs in women and men at homeostasis. Critically ill patients have profound dysregulation of homeostasis and metabolism. It is not clear if the metabolic response to critical illness differs in women compared to men. Such sex-specific differences in illness response would have consequences for personalized medicine. Our aim was to determine the sex-specific metabolomic response to early critical illness. We performed a post-hoc metabolomics study of the VITdAL-ICU trial where subjects received high dose vitamin D3 or placebo. Using mixed-effects modeling, we studied sex-specific changes in metabolites over time adjusted for age, Simplified Acute Physiology Score II, admission diagnosis, day 0 25-hydroxyvitamin D level, and 25-hydroxyvitamin D response to intervention. In women, multiple members of the sphingomyelin and lysophospholipid metabolite classes had significantly positive Bonferroni corrected associations over time compared to men. Further, multiple representatives of the acylcarnitine, androgenic steroid, bile acid, nucleotide and amino acid metabolite classes had significantly negative Bonferroni corrected associations over time compared to men. Gaussian graphical model analyses revealed sex-specific functional modules. Our findings show that robust and coordinated sex-specific metabolite differences exist early in critical illness.
url https://doi.org/10.1038/s41598-021-83602-5
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