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dc.creatorAbilés, Jimenaes
dc.creatorPérez de la Cruz, Antonio Jesúses
dc.creatorCastaño, José Garcíaes
dc.creatorRodríguez Elvira, Manueles
dc.creatorAguayo, Eduardoes
dc.creatorMoreno Torres, Rosarioes
dc.creatorLlopis, Juan Emilioes
dc.creatorAranda, Pilares
dc.creatorArgüelles Castilla, Sandroes
dc.creatorAyala Gómez, Antonioes
dc.creatorMachado Quintana, Albertoes
dc.creatorPlanells, Elena Maríaes
dc.date.accessioned2016-05-24T12:36:43Z
dc.date.available2016-05-24T12:36:43Z
dc.date.issued2006
dc.identifier.citationAbilés, J., Pérez de la Cruz, A.J., Castaño, J.G., Rodríguez Elvira, M., Aguayo, E., Moreno Torres, R.,...,Planells, E.M. (2006). Oxidative stress is increased in critically ill patients according to antioxidant vitamins intake, independent of severity: A cohort study. Critical Care, 10 (5), 1-9.
dc.identifier.issn1466-609Xes
dc.identifier.urihttp://hdl.handle.net/11441/41541
dc.description.abstractCritically ill patients suffer from oxidative stress caused by reactive oxygen species (ROS) and reactive nitrogen species (RNS). Although ROS/RNS are constantly produced under normal circumstances, critical illness can drastically increase their production. These patients have reduced plasma and intracellular levels of antioxidants and free electron scavengers or cofactors, and decreased activity of the enzymatic system involved in ROS detoxification. The prooxidant/ antioxidant balance is of functional relevance during critical illness because it is involved in the pathogenesis of multiple organ failure. In this study the objective was to evaluate the relation between oxidative stress in critically ill patients and antioxidant vitamin intake and severity of illness. Methods Spectrophotometry was used to measure in plasma the total antioxidant capacity and levels of lipid peroxide, carbonyl group, total protein, bilirubin and uric acid at two time points: at intensive care unit (ICU) admission and on day seven. Daily diet records were kept and compliance with recommended dietary allowance (RDA) of antioxidant vitamins (A, C and E) was assessed. Results Between admission and day seven in the ICU, significant increases in lipid peroxide and carbonyl group were associated with decreased antioxidant capacity and greater deterioration in Sequential Organ Failure Assessment score. There was significantly greater worsening in oxidative stress parameters in patients who received antioxidant vitamins at below 66% of RDA than in those who received antioxidant vitamins at above 66% of RDA. An antioxidant vitamin intake from 66% to 100% of RDA reduced the risk for worsening oxidative stress by 94% (ods ratio 0.06, 95% confidence interval 0.010 to 0.39), regardless of change in severity of illness (Sequential Organ Failure Assessment score). Conclusion The critical condition of patients admitted to the ICU is associated with worsening oxidative stress. Intake of antioxidant vitamins below 66% of RDA and alteration in endogenous levels of substances with antioxidant capacity are related to redox imbalance in critical ill patients. Therefore, intake of antioxidant vitamins should be carefully monitored so that it is as close as possible to RDAes
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherSpringer Science + Business Mediaes
dc.relation.ispartofCritical Care, 10 (5), 1-9.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleOxidative stress is increased in critically ill patients according to antioxidant vitamins intake, independent of severity: A cohort studyes
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Bioquímica y Biología Moleculares
dc.relation.publisherversion10.1186/cc5068es
dc.identifier.doihttp://dx.doi.org/10.1186/cc5068es
idus.format.extent9 p.es
dc.journaltitleCritical Carees
dc.publication.volumen10es
dc.publication.issue5es
dc.publication.initialPage1es
dc.publication.endPage9es
dc.identifier.idushttps://idus.us.es/xmlui/handle/11441/41541

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