<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bentley C</submitter><funding>AOUK&amp;amp;I Foundation</funding><funding>National Institute for Health Research - Surgical Reconstruction and Microbiology Research Centre</funding><funding>Cancer Research UK</funding><funding>Queen Elizabeth Hospital Birmingham Charity</funding><funding>Medical Research Council</funding><pagination>e040823</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8314713</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(7)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The improvements in short-term outcome after severe trauma achieved through early resuscitation and acute care can be offset over the following weeks by an acute systemic inflammatory response with immuneparesis leading to infection, multiorgan dysfunction/multiorgan failure (MOF) and death. Serum levels of the androgen precursor dehydroepiandrosterone (DHEA) and its sulfate ester DHEAS, steroids with immune-enhancing activity, are low after traumatic injury at a time when patients are catabolic and immunosuppressed. Addressing this deficit and restoring the DHEA(S) ratio to cortisol may provide a range of physiological benefits, including immune modulatory effects.&lt;h4>Objective&lt;/h4>Our primary objective is to establish a dose suitable for DHEA supplementation in patie</pubmed_abstract><journal>BMJ open</journal><pubmed_title>A prospective, phase II, single-centre, cross-sectional, randomised study investigating Dehydroepiandrosterone supplementation and its Profile in Trauma: ADaPT.</pubmed_title><pmcid>PMC8314713</pmcid><funding_grant_id>n/a</funding_grant_id><funding_grant_id>25354</funding_grant_id><funding_grant_id>MR/K00414X/1</funding_grant_id><funding_grant_id>MR/P021220/1</funding_grant_id><pubmed_authors>Shaheen F</pubmed_authors><pubmed_authors>Bentley C</pubmed_authors><pubmed_authors>Carrera R</pubmed_authors><pubmed_authors>Foster MA</pubmed_authors><pubmed_authors>Toman E</pubmed_authors><pubmed_authors>Greig CA</pubmed_authors><pubmed_authors>Barton D</pubmed_authors><pubmed_authors>Ermogenous C</pubmed_authors><pubmed_authors>Gilligan LC</pubmed_authors><pubmed_authors>Homer V</pubmed_authors><pubmed_authors>Hazeldine J</pubmed_authors><pubmed_authors>Arlt W</pubmed_authors><pubmed_authors>Taylor AE</pubmed_authors><pubmed_authors>Yakoub KM</pubmed_authors><pubmed_authors>Desai A</pubmed_authors><pubmed_authors>Potter C</pubmed_authors><pubmed_authors>Lord JM</pubmed_authors><pubmed_authors>Young K</pubmed_authors><pubmed_authors>McGee K</pubmed_authors><pubmed_authors>Brock K</pubmed_authors><pubmed_authors>Athwal A</pubmed_authors><pubmed_authors>Sur G</pubmed_authors></additional><is_claimable>false</is_claimable><name>A prospective, phase II, single-centre, cross-sectional, randomised study investigating Dehydroepiandrosterone supplementation and its Profile in Trauma: ADaPT.</name><description>&lt;h4>Introduction&lt;/h4>The improvements in short-term outcome after severe trauma achieved through early resuscitation and acute care can be offset over the following weeks by an acute systemic inflammatory response with immuneparesis leading to infection, multiorgan dysfunction/multiorgan failure (MOF) and death. Serum levels of the androgen precursor dehydroepiandrosterone (DHEA) and its sulfate ester DHEAS, steroids with immune-enhancing activity, are low after traumatic injury at a time when patients are catabolic and immunosuppressed. Addressing this deficit and restoring the DHEA(S) ratio to cortisol may provide a range of physiological benefits, including immune modulatory effects.&lt;h4>Objective&lt;/h4>Our primary objective is to establish a dose suitable for DHEA supplementation in patie</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2026-05-08T10:04:57.442Z</modification><creation>2022-02-11T07:10:31.779Z</creation></dates><accession>S-EPMC8314713</accession><cross_references><pubmed>34312190</pubmed><doi>10.1136/bmjopen-2020-040823</doi></cross_references></HashMap>