Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/10068
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dc.contributor.authorPapathanassoglou, Elizabeth-
dc.contributor.authorMpouzika, Meropi-
dc.contributor.authorGiannakopoulou, Margarita-
dc.contributor.authorBozas, Evangelos-
dc.contributor.authorMiddleton, Nicos-
dc.contributor.authorTsiaousis, George Z.-
dc.contributor.authorKarabinis, Andreas P.-
dc.date.accessioned2017-04-25T11:44:07Z-
dc.date.available2017-04-25T11:44:07Z-
dc.date.issued2017-01-13-
dc.identifier.citationJournal of Pain Research, 2017, vol. 10, pp. 175-181en_US
dc.identifier.issn11787090-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/10068-
dc.description.abstractObjective: Lymphocyte apoptosis in critical illness is associated with immunosuppression. We explored for the first time the associations between pain ratings and expression of the apoptotic receptor Fas on B and T cells in critically ill patients and the potential mediating effects of adrenocorticotropic hormone (ACTH), cortisol, and substance P (SP). Design: This is an exploratory correlational study with repeated measurements (14 days followup) and cross-sectional comparisons. Setting: This study was conducted in a state hospital in the metropolitan area of Athens, Greece. Participants: The participants were 36 consecutive critically ill patients and 36 matched controls. Outcome measures: Pain measured by the self-reported numeric rating scale [NRS], the behavioral pain scale, and the pain assessment scale was the primary outcome measure. Flow cytometry (Fas), electrochemiluminescence (ACTH and cortisol) and enzyme-linked immunosorbent assay (SP) were used. Mixed linear models for repeated measurements and bivariable associations at discrete time points were employed. Results: Significant pain at rest was noted. Pain ratings associated with Fas expression on cytotoxic T cells (P=0.041) and B cells (P=0.005), even after adjustment for a number of clinical treatment factors (P=0.006 and P=0.052, respectively). On the day that more patients were able to communicate, Fas on B cells (r=0.897, P=0.029) and cytotoxic T cells (r=0.832; P=0.037) associated with NRS ratings. Associations between pain ratings and ACTH serum levels were noted (P<0.05). When stress neuropeptide levels were added to the model, the statistical significance of the associations between pain ratings and Fas expression was attenuated (P=0.052–0.063), suggesting that stress neuropeptides may partially mediate the association. Conclusion: Preliminary evidence for the association between pain and lymphocyte apoptotic susceptibility is provided. The role of pain management in maintaining immunocompetence in critical illness is worth exploring.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Pain Researchen_US
dc.rights© Papathanassoglou et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms. php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License . By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.en_US
dc.subjectAdrenocorticotropic hormoneen_US
dc.subjectCortisolen_US
dc.subjectCritical illnessen_US
dc.subjectLymphocyte apoptosisen_US
dc.subjectPainen_US
dc.subjectSubstance Pen_US
dc.titleAssociation between lymphocyte expression of the apoptotic receptor Fas and pain in critically ill patientsen_US
dc.typeArticleen_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationNational and Kapodistrian University of Athensen_US
dc.collaborationOnassis Cardiac Surgery Centeren_US
dc.collaborationUniversity of Albertaen_US
dc.subject.categoryHealth Sciencesen_US
dc.journalsOpen Accessen_US
dc.countryCyprusen_US
dc.countryGreeceen_US
dc.countryCanadaen_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.2147/JPR.S118105en_US
dc.relation.volume10en_US
cut.common.academicyear2016-2017en_US
dc.identifier.spage175en_US
dc.identifier.epage181en_US
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.languageiso639-1en-
crisitem.journal.journalissn1178-7090-
crisitem.journal.publisherDove Medical Press-
crisitem.author.deptDepartment of Nursing-
crisitem.author.deptDepartment of Nursing-
crisitem.author.deptDepartment of Nursing-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0002-7439-1492-
crisitem.author.orcid0000-0001-7730-940X-
crisitem.author.orcid0000-0001-6358-8591-
crisitem.author.parentorgFaculty of Health Sciences-
crisitem.author.parentorgFaculty of Health Sciences-
crisitem.author.parentorgFaculty of Health Sciences-
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