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dc.creatorDardiotis E., Siokas V., Aloizou A.-M., Karampinis E., Brotis A.G., Grigoriadis S., Paterakis K., Dardioti M., Komnos A., Kapsalaki E., Fountas K., Hadjigeorgiou G.M.en
dc.date.accessioned2023-01-31T07:50:58Z
dc.date.available2023-01-31T07:50:58Z
dc.date.issued2019
dc.identifier10.1080/02699052.2019.1606444
dc.identifier.issn02699052
dc.identifier.urihttp://hdl.handle.net/11615/73092
dc.description.abstractBackground: Α few genetic variants are associated with the outcome after traumatic brain injury (TBI). Integrins are glycoprotein receptors that play an important role in the integrity of microvasculature of the brain. Objective: To examine the role of integrin-AV (ITGAV) and integrin-B8 (ITGB8) tag single nucleotide polymorphisms (SNPs) on the outcome of patients with TBI. Methods: 363 participants were included and genotyped for 11 SNPs for ITGAV and 11 for ITGB8 gene. SNPs were tested for associations with the 6-month outcome after TBI, the presence of a hemorrhagic event after TBI, and the initial TBI severity after adjustment for TBI’s main predictors. Results: The ITGAV rs3911239 CC and rs7596996 GG genotypes were associated with an unfavorable outcome after TBI, compared to the TT and AA genotypes, respectively. The ITGB8 rs10239099 CC and rs3757727 CC genotypes were associated with increased risk of any cerebral hemorrhagic event after TBI compared to GG and TT respectively. The ITGAV rs7589470 and rs7565633 were associated with the TBI’s initial severity. Conclusions: ITGAV gene SNPs may be implicated in the outcome after TBI, as well as in the initial TBI severity, and also of ITGB8 gene SNPs in the risk of hemorrhagic event after a TBI. © 2019, © 2019 Taylor & Francis Group, LLC.en
dc.language.isoenen
dc.sourceBrain Injuryen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85065185506&doi=10.1080%2f02699052.2019.1606444&partnerID=40&md5=a1fa23a01cba841eef6fafcbc242488c
dc.subjectintegrinen
dc.subjectbeta integrinen
dc.subjectCD51 antigenen
dc.subjectintegrin beta8en
dc.subjectadulten
dc.subjectalleleen
dc.subjectArticleen
dc.subjectassociationen
dc.subjectbrain hemorrhageen
dc.subjectclinical outcomeen
dc.subjectcohort analysisen
dc.subjectdisease severityen
dc.subjectDNA polymorphismen
dc.subjectfemaleen
dc.subjectgenotypeen
dc.subjectheterozygosityen
dc.subjecthomozygosityen
dc.subjecthumanen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectmutational loaden
dc.subjectregression analysisen
dc.subjectsingle nucleotide polymorphismen
dc.subjecttraumatic brain injuryen
dc.subjectx-ray computed tomographyen
dc.subjectadolescenten
dc.subjectageden
dc.subjectbrain hemorrhageen
dc.subjectcomplicationen
dc.subjectgeneticsen
dc.subjectgenotypeen
dc.subjectmiddle ageden
dc.subjectsingle nucleotide polymorphismen
dc.subjecttraumatic brain injuryen
dc.subjectvery elderlyen
dc.subjectyoung adulten
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectAgeden
dc.subjectAged, 80 and overen
dc.subjectBrain Injuries, Traumaticen
dc.subjectCerebral Hemorrhageen
dc.subjectFemaleen
dc.subjectGenotypeen
dc.subjectHumansen
dc.subjectIntegrin alphaVen
dc.subjectIntegrin beta Chainsen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectPolymorphism, Single Nucleotideen
dc.subjectYoung Adulten
dc.subjectTaylor and Francis Ltden
dc.titleEffect of integrin AV and B8 gene polymorphisms in patients with traumatic brain injuryen
dc.typejournalArticleen


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