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Sex, sepsis and the brain: defining the role of sexual dimorphism on neurocognitive outcomes after infection
Sexual dimorphisms exist in multiple domains, from learning and memory to neurocognitive disease, and even in the immune system. Male sex has been associated with increased susceptibility to infection, as well as increased risk of adverse outcomes. Sepsis remains a major source of morbidity and mort...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285043/ https://www.ncbi.nlm.nih.gov/pubmed/37337946 http://dx.doi.org/10.1042/CS20220555 |
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author | Polcz, Valerie E. Barrios, Evan L. Chapin, Benjamin Price, Catherine C. Nagpal, Ravinder Chakrabarty, Paramita Casadesus, Gemma Foster, Thomas Moldawer, Lyle L. Efron, Philip A. |
author_facet | Polcz, Valerie E. Barrios, Evan L. Chapin, Benjamin Price, Catherine C. Nagpal, Ravinder Chakrabarty, Paramita Casadesus, Gemma Foster, Thomas Moldawer, Lyle L. Efron, Philip A. |
author_sort | Polcz, Valerie E. |
collection | PubMed |
description | Sexual dimorphisms exist in multiple domains, from learning and memory to neurocognitive disease, and even in the immune system. Male sex has been associated with increased susceptibility to infection, as well as increased risk of adverse outcomes. Sepsis remains a major source of morbidity and mortality globally, and over half of septic patients admitted to intensive care are believed to suffer some degree of sepsis-associated encephalopathy (SAE). In the short term, SAE is associated with an increased risk of in-hospital mortality, and in the long term, has the potential for significant impairment of cognition, memory, and acceleration of neurocognitive disease. Despite increasing information regarding sexual dimorphism in neurologic and immunologic systems, research into these dimorphisms in sepsis-associated encephalopathy remains critically understudied. In this narrative review, we discuss how sex has been associated with brain morphology, chemistry, and disease, sexual dimorphism in immunity, and existing research into the effects of sex on SAE. |
format | Online Article Text |
id | pubmed-10285043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102850432023-06-23 Sex, sepsis and the brain: defining the role of sexual dimorphism on neurocognitive outcomes after infection Polcz, Valerie E. Barrios, Evan L. Chapin, Benjamin Price, Catherine C. Nagpal, Ravinder Chakrabarty, Paramita Casadesus, Gemma Foster, Thomas Moldawer, Lyle L. Efron, Philip A. Clin Sci (Lond) Gene Expression & Regulation Sexual dimorphisms exist in multiple domains, from learning and memory to neurocognitive disease, and even in the immune system. Male sex has been associated with increased susceptibility to infection, as well as increased risk of adverse outcomes. Sepsis remains a major source of morbidity and mortality globally, and over half of septic patients admitted to intensive care are believed to suffer some degree of sepsis-associated encephalopathy (SAE). In the short term, SAE is associated with an increased risk of in-hospital mortality, and in the long term, has the potential for significant impairment of cognition, memory, and acceleration of neurocognitive disease. Despite increasing information regarding sexual dimorphism in neurologic and immunologic systems, research into these dimorphisms in sepsis-associated encephalopathy remains critically understudied. In this narrative review, we discuss how sex has been associated with brain morphology, chemistry, and disease, sexual dimorphism in immunity, and existing research into the effects of sex on SAE. Portland Press Ltd. 2023-06 2023-06-20 /pmc/articles/PMC10285043/ /pubmed/37337946 http://dx.doi.org/10.1042/CS20220555 Text en © 2023 The Author(s). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . Open access for this article was enabled by the participation of University of Florida in an all-inclusive Read & Publish agreement with Portland Press and the Biochemical Society under a transformative agreement with Individual. |
spellingShingle | Gene Expression & Regulation Polcz, Valerie E. Barrios, Evan L. Chapin, Benjamin Price, Catherine C. Nagpal, Ravinder Chakrabarty, Paramita Casadesus, Gemma Foster, Thomas Moldawer, Lyle L. Efron, Philip A. Sex, sepsis and the brain: defining the role of sexual dimorphism on neurocognitive outcomes after infection |
title | Sex, sepsis and the brain: defining the role of sexual dimorphism on neurocognitive outcomes after infection |
title_full | Sex, sepsis and the brain: defining the role of sexual dimorphism on neurocognitive outcomes after infection |
title_fullStr | Sex, sepsis and the brain: defining the role of sexual dimorphism on neurocognitive outcomes after infection |
title_full_unstemmed | Sex, sepsis and the brain: defining the role of sexual dimorphism on neurocognitive outcomes after infection |
title_short | Sex, sepsis and the brain: defining the role of sexual dimorphism on neurocognitive outcomes after infection |
title_sort | sex, sepsis and the brain: defining the role of sexual dimorphism on neurocognitive outcomes after infection |
topic | Gene Expression & Regulation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285043/ https://www.ncbi.nlm.nih.gov/pubmed/37337946 http://dx.doi.org/10.1042/CS20220555 |
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