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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2023
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.
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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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