Εμφάνιση απλής εγγραφής

dc.creatorDimou N.L., Pantavou K.G., Bagos P.G.en
dc.date.accessioned2023-01-31T07:56:46Z
dc.date.available2023-01-31T07:56:46Z
dc.date.issued2017
dc.identifier10.1111/ahg.12203
dc.identifier.issn00034800
dc.identifier.urihttp://hdl.handle.net/11615/73358
dc.description.abstractApolipoprotein E (ApoE) is potentially a genetic risk factor for the development of left ventricular failure (LVF), the main cause of death in beta-thalassemia homozygotes. In the present study, we synthesize the results of independent studies examining the effect of ApoE on LVF development in thalassemic patients through a meta-analytic approach. However, all studies report more than one outcome, as patients are classified into three groups according to the severity of the symptoms and the genetic polymorphism. Thus, a multivariate meta-analytic method that addresses simultaneously multiple exposures and multiple comparison groups was developed. Four individual studies were included in the meta-analysis involving 613 beta-thalassemic patients and 664 controls. The proposed method that takes into account the correlation of log odds ratios (log(ORs)), revealed a statistically significant overall association (P-value = 0.009), mainly attributed to the contrast of E4 versus E3 allele for patients with evidence (OR: 2.32, 95% CI: 1.19, 4.53) or patients with clinical and echocardiographic findings (OR: 3.34, 95% CI: 1.78, 6.26) of LVF. This study suggests that E4 is a genetic risk factor for LVF in beta-thalassemia major. The presented multivariate approach can be applied in several fields of research. © 2017 John Wiley & Sons Ltd/University College Londonen
dc.language.isoenen
dc.sourceAnnals of Human Geneticsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85021812805&doi=10.1111%2fahg.12203&partnerID=40&md5=ba4646cea55a02a84b9116812b28215a
dc.subjectapolipoprotein Een
dc.subjectapolipoprotein Een
dc.subjectalleleen
dc.subjectApoE geneen
dc.subjectArticleen
dc.subjectbeta thalassemiaen
dc.subjectdisease severityen
dc.subjectechocardiographyen
dc.subjectgeneen
dc.subjectgenetic associationen
dc.subjectgenetic polymorphismen
dc.subjectgenetic risken
dc.subjectheart left ventricle failureen
dc.subjecthomozygoteen
dc.subjecthumanen
dc.subjectmultivariate analysisen
dc.subjectpriority journalen
dc.subjectsymptomatologyen
dc.subjectadolescenten
dc.subjectadulten
dc.subjectbeta thalassemiaen
dc.subjectchilden
dc.subjectcomplicationen
dc.subjectfemaleen
dc.subjectgenetic predispositionen
dc.subjectgeneticsen
dc.subjectheart left ventricle functionen
dc.subjectmaleen
dc.subjectmeta analysisen
dc.subjectmiddle ageden
dc.subjectpathophysiologyen
dc.subjectpreschool childen
dc.subjectrisk factoren
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectApolipoproteins Een
dc.subjectbeta-Thalassemiaen
dc.subjectChilden
dc.subjectChild, Preschoolen
dc.subjectFemaleen
dc.subjectGenetic Predisposition to Diseaseen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectMultivariate Analysisen
dc.subjectPolymorphism, Geneticen
dc.subjectRisk Factorsen
dc.subjectVentricular Function, Leften
dc.subjectBlackwell Publishing Ltden
dc.titleApolipoprotein E Polymorphism and Left Ventricular Failure in Beta-Thalassemia: A Multivariate Meta-Analysisen
dc.typejournalArticleen


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