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dc.contributor.authorDhanda, Ashwin
dc.contributor.authorAtkinson, S
dc.contributor.authorVergis, N
dc.contributor.authorEnki, D
dc.contributor.authorEKİM DERTLİ, Samiye
dc.contributor.authorClough, Robert
dc.contributor.authorCramp, Matthew
dc.contributor.authorThursz, M
dc.date.accessioned2020-07-09T13:55:45Z
dc.date.issued2020-06-23
dc.identifier.issn0269-2813
dc.identifier.issn1365-2036
dc.identifier.urihttp://hdl.handle.net/10026.1/15950
dc.description.abstract

<jats:title>Summary</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Malnutrition is common in patients with alcohol‐related liver disease and is associated with outcome in patients with alcoholic hepatitis. Trace elements (cobalt, copper, iron, selenium and zinc) are micronutrients essential for many cellular processes including antioxidant pathways. The prevalence and relevance of trace element deficiency is unknown in alcoholic hepatitis.</jats:p></jats:sec><jats:sec><jats:title>Aim</jats:title><jats:p>To determine the prevalence of trace element deficiency and its association with clinical outcomes in patients with alcoholic hepatitis.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Serum was obtained from patients with alcoholic hepatitis, alcohol‐related cirrhosis and healthy volunteers as part of clinical trials, cohort studies and a biobank. Trace element concentration was measured by inductively coupled plasma mass spectrometry. Association of trace element levels with development of infection within 90 days and mortality within 28 and 90 days was evaluated by multivariate logistic regression.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Sera from 302 patients with alcoholic hepatitis, 46 with alcohol‐related cirrhosis and 15 healthy controls were analysed for trace element concentration. The prevalence of zinc deficiency (85%) and selenium deficiency (67%) in alcoholic hepatitis was higher than in alcohol‐related cirrhosis (72% [p=0.04] and 37% [p&lt;0.001], respectively). Zinc, selenium, copper and chromium were significantly different between groups. Iron deficiency was a predictor of development of infection within 90 days. Zinc deficiency was a predictor of mortality within 28 and 90 days.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Trace element deficiency in patients with alcoholic hepatitis is highly prevalent and associated with infection and mortality. Supplementation with selected trace elements may improve clinical outcomes in this patient group but further insight is required of their biological and clinical effects.</jats:p></jats:sec>

dc.format.extent537-544
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoen
dc.publisherWiley
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAdult
dc.subjectAged
dc.subjectFemale
dc.subjectHepatitis, Alcoholic
dc.subjectHumans
dc.subjectInfections
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectPrevalence
dc.subjectTrace Elements
dc.subjectYoung Adult
dc.titleTrace element deficiency is highly prevalent and associated with infection and mortality in patients with alcoholic hepatitis
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000541820400001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue3
plymouth.volume52
plymouth.publication-statusPublished
plymouth.journalAlimentary Pharmacology & Therapeutics
dc.identifier.doi10.1111/apt.15880
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/BEACh
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CBR
plymouth.organisational-group/Plymouth/Research Groups/Plymouth Institute of Health and Care Research (PIHR)
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeEngland
dcterms.dateAccepted2020-05-22
dc.rights.embargodate2021-6-23
dc.identifier.eissn1365-2036
dc.rights.embargoperiodNot known
rioxxterms.funderMedical Research Council
rioxxterms.identifier.projectMICA: Minimising Mortality from Alcoholic Hepatitis
rioxxterms.versionofrecord10.1111/apt.15880
rioxxterms.licenseref.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
rioxxterms.licenseref.startdate2020-06-23
rioxxterms.typeJournal Article/Review
plymouth.funderMICA: Minimising Mortality from Alcoholic Hepatitis::Medical Research Council


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