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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
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Effect of integrin AV and B8 gene polymorphisms in patients with traumatic brain injury

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Author
Dardiotis 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.
Date
2019
Language
en
DOI
10.1080/02699052.2019.1606444
Keyword
integrin
beta integrin
CD51 antigen
integrin beta8
adult
allele
Article
association
brain hemorrhage
clinical outcome
cohort analysis
disease severity
DNA polymorphism
female
genotype
heterozygosity
homozygosity
human
major clinical study
male
mutational load
regression analysis
single nucleotide polymorphism
traumatic brain injury
x-ray computed tomography
adolescent
aged
brain hemorrhage
complication
genetics
genotype
middle aged
single nucleotide polymorphism
traumatic brain injury
very elderly
young adult
Adolescent
Adult
Aged
Aged, 80 and over
Brain Injuries, Traumatic
Cerebral Hemorrhage
Female
Genotype
Humans
Integrin alphaV
Integrin beta Chains
Male
Middle Aged
Polymorphism, Single Nucleotide
Young Adult
Taylor and Francis Ltd
Metadata display
Abstract
Background: 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.
URI
http://hdl.handle.net/11615/73092
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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