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Προβολή τεκμηρίου 
  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Apolipoprotein E Polymorphism and Left Ventricular Failure in Beta-Thalassemia: A Multivariate Meta-Analysis

Thumbnail
Συγγραφέας
Dimou N.L., Pantavou K.G., Bagos P.G.
Ημερομηνία
2017
Γλώσσα
en
DOI
10.1111/ahg.12203
Λέξη-κλειδί
apolipoprotein E
apolipoprotein E
allele
ApoE gene
Article
beta thalassemia
disease severity
echocardiography
gene
genetic association
genetic polymorphism
genetic risk
heart left ventricle failure
homozygote
human
multivariate analysis
priority journal
symptomatology
adolescent
adult
beta thalassemia
child
complication
female
genetic predisposition
genetics
heart left ventricle function
male
meta analysis
middle aged
pathophysiology
preschool child
risk factor
Adolescent
Adult
Apolipoproteins E
beta-Thalassemia
Child
Child, Preschool
Female
Genetic Predisposition to Disease
Humans
Male
Middle Aged
Multivariate Analysis
Polymorphism, Genetic
Risk Factors
Ventricular Function, Left
Blackwell Publishing Ltd
Εμφάνιση Μεταδεδομένων
Επιτομή
Apolipoprotein 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 London
URI
http://hdl.handle.net/11615/73358
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19674]

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Η δικτυακή πύλη της Ευρωπαϊκής Ένωσης
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ΕΣΠΑ 2007-2013
Με τη συγχρηματοδότηση της Ελλάδας και της Ευρωπαϊκής Ένωσης
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