Show simple item record

 
dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorAlijotas-Reig, Jaume
dc.contributor.authorMorales-Pérez, Stephanie
dc.contributor.authorRivero-Santana, Sergio
dc.contributor.authorMarques Soares, Joana Rita
dc.contributor.authorAnunciación-Llunell, Ariadna
dc.contributor.authorEsteve-Valverde, Enrique
dc.contributor.authorTrape, Jaume
dc.contributor.authorMiro-Mur, Francesc A.
dc.date.accessioned2024-04-05T07:30:53Z
dc.date.available2024-04-05T07:30:53Z
dc.date.issued2024-03-05
dc.identifier.citationAlijotas-Reig J, Anunciacion-Llunell A, Esteve-Valverde E, Morales-Pérez S, Rivero-Santana S, Trapé J, et al. Pituitary–Adrenal Axis and Peripheral Immune Cell Profile in Long COVID. Biomedicines. 2024 Mar 5;12(3):581.
dc.identifier.issn2227-9059
dc.identifier.urihttps://hdl.handle.net/11351/11286
dc.descriptionLong COVID; Adrenal insufficiency; Inflammation
dc.description.abstractIn Long COVID, dysfunction in the pituitary–adrenal axis and alterations in immune cells and inflammatory status are warned against. We performed a prospective study in a cohort of 42 patients who suffered COVID-19 at least 6 months before attending the Long COVID unit at Althaia Hospital. Based on Post-COVID Functional Status, 29 patients were diagnosed with Long COVID, while 13 were deemed as recovered. The hormones of the pituitary–adrenal axis, adrenocorticotropin stimulation test, and immune cell profiles and inflammatory markers were examined. Patients with Long COVID had significantly lower EuroQol and higher mMRC scores compared to the recovered individuals. Their symptoms included fatigue, myalgia, arthralgia, persistent coughing, a persistent sore throat, dyspnoea, a lack of concentration, and anxiety. We observed the physiological levels of cortisol and adrenocorticotropin in individuals with or without Long COVID. The results of the adrenocorticotropin stimulation test were similar between both groups. The absolute number of neutrophils was lower in the Long COVID patients compared to recovered individuals (p < 0.05). The total count of B lymphocytes remained consistent, but Long COVID patients had a higher percentage of mature B cells compared to recovered participants (p < 0.05) and exhibited a higher percentage of circulating resident memory CD8+ T cells (p < 0.05) and Treg-expressing exonucleases (p < 0.05). Our findings did not identify adrenal dysfunction related to Long COVID, nor an association between adrenal function and clinical symptoms. The data indicated a dysregulation in certain immune cells, pointing to immune activation. No overt hyperinflammation was observed in the Long COVID group.
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesBiomedicines;12(3)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectCOVID-19 (Malaltia) - Complicacions
dc.subjectDispnea
dc.subjectGlàndules suprarenals - Malalties
dc.subjectACTH
dc.subject.meshCoronavirus Infections
dc.subject.mesh/complications
dc.subject.meshAdrenocorticotropic Hormone
dc.subject.meshAdrenal Insufficiency
dc.subject.meshDyspnea
dc.titlePituitary–Adrenal Axis and Peripheral Immune Cell Profile in Long COVID
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/biomedicines12030581
dc.subject.decsinfecciones por Coronavirus
dc.subject.decs/complicaciones
dc.subject.decscorticotropina
dc.subject.decsinsuficiencia suprarrenal
dc.subject.decsdisnea
dc.relation.publishversionhttps://doi.org/10.3390/biomedicines12030581
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Alijotas-Reig J, Marques-Soares J] Unitat de Recerca de Malalties Autoimmunes Sistèmiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Unitat de Malalties Autoimmunes Sistèmiques, Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Departament de Medicina, Facultat de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Anunciacion-Llunell A, Miro-Mur F] Unitat de Recerca de Malalties Autoimmunes Sistèmiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Esteve-Valverde E] Departament de Medicina, Facultat de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain. Systemic Autoimmune Diseases Unit, Department of Internal Medicine, Hospital Universitari Parc Taulí, Sabadell, Spain. [Morales-Pérez S, Rivero-Santana S] Systemic Autoimmune Disease Unit, Internal Medicine Department, Althaia Healthcare University Network of Manresa, Manresa, Spain. [Trapé J] Laboratory Medicine, Althaia Healthcare University Network of Manresa, Manresa, Spain. Tissue Repair and Regeneration Laboratory (TR2Lab), Institut de Recerca i Innovació en Ciències de la Vida i de la Salut a la Catalunya Central (IrisCC), Barcelona, Spain
dc.identifier.pmid38540194
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record