Εμφάνιση απλής εγγραφής

dc.creatorSpeletas M., Dadouli K., Syrakouli A., Gatselis N., Germanidis G., Mouchtouri V.A., Koulas I., Samakidou A., Nikolaidou A., Stefos A., Mimtsoudis I., Hatzianastasiou S., Koureas M., Anagnostopoulos L., Tseroni M., Tsinti G., Metallidis S., Dalekos G., Hadjichristodoulou C.en
dc.date.accessioned2023-01-31T10:01:11Z
dc.date.available2023-01-31T10:01:11Z
dc.date.issued2021
dc.identifier10.1016/j.imbio.2021.152136
dc.identifier.issn01712985
dc.identifier.urihttp://hdl.handle.net/11615/79322
dc.description.abstractThe COVID-19 pandemic represents one of the greatest challenges in modern medicine. The disease is characterized by a variable clinical phenotype, ranging from asymptomatic carriage to severe and/or critical disease, which bears poor prognosis and outcome because of the development of severe acute respiratory distress syndrome (SARS) requiring ICU hospitalization, multi-organ failure and death. Therefore, the determination of risk factors predisposing to disease phenotype is of outmost importance. The aim of our study was to evaluate which predisposing factors, including MBL2 genotyping, affected clinical phenotype in 264 COVID-19 patients. We demonstrated that older age along with underlying comorbidities, primarily obesity, chronic inflammatory disorders and diabetes mellitus, represent the most important risk factors related to hospitalization, the development of pneumonia and SARS. Moreover, we found that the presence of the MBL deficiency-causing B allele (rs1800450) was significantly associated with almost 2-fold increased risk for developing pneumonia and requiring hospitalization, suggesting its usage as a molecular predictor of severe disease in SARS-CoV-2 infected individuals. © 2021 Elsevier GmbHen
dc.language.isoenen
dc.sourceImmunobiologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85116570903&doi=10.1016%2fj.imbio.2021.152136&partnerID=40&md5=8e40e878879ba3525e996275b189b1c5
dc.subjectmannose binding lectinen
dc.subjectmannose binding lectinen
dc.subjectMBL2 protein, humanen
dc.subjectadulten
dc.subjectalleleen
dc.subjectArticleen
dc.subjectcausal attributionen
dc.subjectchronic inflammationen
dc.subjectcomorbidityen
dc.subjectcoronavirus disease 2019en
dc.subjectdiabetes mellitusen
dc.subjectdisease predispositionen
dc.subjectdisease severityen
dc.subjectfemaleen
dc.subjecthospitalizationen
dc.subjecthumanen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectobesityen
dc.subjectphenotypeen
dc.subjectpneumoniaen
dc.subjectprotein deficiencyen
dc.subjectrisk assessmenten
dc.subjectrisk factoren
dc.subjectsingle nucleotide polymorphismen
dc.subjectageden
dc.subjectgeneticsen
dc.subjectmiddle ageden
dc.subjectseverity of illness indexen
dc.subjectyoung adulten
dc.subjectAdulten
dc.subjectAgeden
dc.subjectAllelesen
dc.subjectComorbidityen
dc.subjectCOVID-19en
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectMannose-Binding Lectinen
dc.subjectMiddle Ageden
dc.subjectPhenotypeen
dc.subjectRisk Factorsen
dc.subjectSeverity of Illness Indexen
dc.subjectYoung Adulten
dc.subjectElsevier GmbHen
dc.titleMBL deficiency-causing B allele (rs1800450) as a risk factor for severe COVID-19en
dc.typejournalArticleen


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