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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2021-02-01
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Online Access: | https://doi.org/10.1038/s41598-021-83602-5 |
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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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