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Comparison of Transcriptomic Changes in Survivors of Exertional Heat Illness with Malignant Hyperthermia Susceptible Patients

Exertional heat illness (EHI) is an occupational health hazard for athletes and military personnel–characterised by the inability to thermoregulate during exercise. The ability to thermoregulate can be studied using a standardised heat tolerance test (HTT) developed by The Institute of Naval Medicin...

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Autores principales: Chang, Leon, Gardner, Lois, House, Carol, Daly, Catherine, Allsopp, Adrian, Roiz de Sa, Daniel, Shaw, Marie-Anne, Hopkins, Philip M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671540/
https://www.ncbi.nlm.nih.gov/pubmed/38003313
http://dx.doi.org/10.3390/ijms242216124
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author Chang, Leon
Gardner, Lois
House, Carol
Daly, Catherine
Allsopp, Adrian
Roiz de Sa, Daniel
Shaw, Marie-Anne
Hopkins, Philip M.
author_facet Chang, Leon
Gardner, Lois
House, Carol
Daly, Catherine
Allsopp, Adrian
Roiz de Sa, Daniel
Shaw, Marie-Anne
Hopkins, Philip M.
author_sort Chang, Leon
collection PubMed
description Exertional heat illness (EHI) is an occupational health hazard for athletes and military personnel–characterised by the inability to thermoregulate during exercise. The ability to thermoregulate can be studied using a standardised heat tolerance test (HTT) developed by The Institute of Naval Medicine. In this study, we investigated whole blood gene expression (at baseline, 2 h post-HTT and 24 h post-HTT) in male subjects with either a history of EHI or known susceptibility to malignant hyperthermia (MHS): a pharmacogenetic condition with similar clinical phenotype. Compared to healthy controls at baseline, 291 genes were differentially expressed in the EHI cohort, with functional enrichment in inflammatory response genes (up to a four-fold increase). In contrast, the MHS cohort featured 1019 differentially expressed genes with significant down-regulation of genes associated with oxidative phosphorylation (OXPHOS). A number of differentially expressed genes in the inflammation and OXPHOS pathways overlapped between the EHI and MHS subjects, indicating a common underlying pathophysiology. Transcriptome profiles between subjects who passed and failed the HTT (based on whether they achieved a plateau in core temperature or not, respectively) were not discernable at baseline, and HTT was shown to elevate inflammatory response gene expression across all clinical phenotypes.
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spelling pubmed-106715402023-11-09 Comparison of Transcriptomic Changes in Survivors of Exertional Heat Illness with Malignant Hyperthermia Susceptible Patients Chang, Leon Gardner, Lois House, Carol Daly, Catherine Allsopp, Adrian Roiz de Sa, Daniel Shaw, Marie-Anne Hopkins, Philip M. Int J Mol Sci Article Exertional heat illness (EHI) is an occupational health hazard for athletes and military personnel–characterised by the inability to thermoregulate during exercise. The ability to thermoregulate can be studied using a standardised heat tolerance test (HTT) developed by The Institute of Naval Medicine. In this study, we investigated whole blood gene expression (at baseline, 2 h post-HTT and 24 h post-HTT) in male subjects with either a history of EHI or known susceptibility to malignant hyperthermia (MHS): a pharmacogenetic condition with similar clinical phenotype. Compared to healthy controls at baseline, 291 genes were differentially expressed in the EHI cohort, with functional enrichment in inflammatory response genes (up to a four-fold increase). In contrast, the MHS cohort featured 1019 differentially expressed genes with significant down-regulation of genes associated with oxidative phosphorylation (OXPHOS). A number of differentially expressed genes in the inflammation and OXPHOS pathways overlapped between the EHI and MHS subjects, indicating a common underlying pathophysiology. Transcriptome profiles between subjects who passed and failed the HTT (based on whether they achieved a plateau in core temperature or not, respectively) were not discernable at baseline, and HTT was shown to elevate inflammatory response gene expression across all clinical phenotypes. MDPI 2023-11-09 /pmc/articles/PMC10671540/ /pubmed/38003313 http://dx.doi.org/10.3390/ijms242216124 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chang, Leon
Gardner, Lois
House, Carol
Daly, Catherine
Allsopp, Adrian
Roiz de Sa, Daniel
Shaw, Marie-Anne
Hopkins, Philip M.
Comparison of Transcriptomic Changes in Survivors of Exertional Heat Illness with Malignant Hyperthermia Susceptible Patients
title Comparison of Transcriptomic Changes in Survivors of Exertional Heat Illness with Malignant Hyperthermia Susceptible Patients
title_full Comparison of Transcriptomic Changes in Survivors of Exertional Heat Illness with Malignant Hyperthermia Susceptible Patients
title_fullStr Comparison of Transcriptomic Changes in Survivors of Exertional Heat Illness with Malignant Hyperthermia Susceptible Patients
title_full_unstemmed Comparison of Transcriptomic Changes in Survivors of Exertional Heat Illness with Malignant Hyperthermia Susceptible Patients
title_short Comparison of Transcriptomic Changes in Survivors of Exertional Heat Illness with Malignant Hyperthermia Susceptible Patients
title_sort comparison of transcriptomic changes in survivors of exertional heat illness with malignant hyperthermia susceptible patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671540/
https://www.ncbi.nlm.nih.gov/pubmed/38003313
http://dx.doi.org/10.3390/ijms242216124
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