Apolipoprotein B gene polymorphisms in patients from Serbia with ischemic cerebrovascular disease

The plasma concentration of apoB has recently been reported to be the best lipid predictor of coronary heart disease. The possible associations of genetic markers in the apolipoprotein B gene (XbaI, EcoRI, MspI, Ins/Del, and 4311 A/G polymorphisms) were evaluated in patients with ischemic cerebrovas...

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Main Authors: Stanković Aleksandra, Stanković Sanja, Jovanović-Marković Zagorka, Živković Maja, Đurić Tamara, Glišić-Milosavljević Sanja, Alavantić D.
Format: Article
Language:English
Published: University of Belgrade, University of Novi Sad 2007-01-01
Series:Archives of Biological Sciences
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0354-4664/2007/0354-46640704303S.pdf
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spelling doaj-49f9fd9477b440fb81879fde0f37fe4d2020-11-24T22:49:35ZengUniversity of Belgrade, University of Novi SadArchives of Biological Sciences0354-46642007-01-0159430330910.2298/ABS0704303SApolipoprotein B gene polymorphisms in patients from Serbia with ischemic cerebrovascular diseaseStanković AleksandraStanković SanjaJovanović-Marković ZagorkaŽivković MajaĐurić TamaraGlišić-Milosavljević SanjaAlavantić D.The plasma concentration of apoB has recently been reported to be the best lipid predictor of coronary heart disease. The possible associations of genetic markers in the apolipoprotein B gene (XbaI, EcoRI, MspI, Ins/Del, and 4311 A/G polymorphisms) were evaluated in patients with ischemic cerebrovascular disease (ICVD) and controls of equivalent BMI. The odds ratio for ICVD in the X+X+ genotype was 2.22, 95% CI 1.24-3.96 (P<0.05), while that for ICVD in the Ins/Ins genotype was 2.82, 95% CI 1.57-5.06 (P<0.05). The patients had significantly higher frequency of the 4311A allele compared to the controls (P<0.01). Our results support the assumption that apoB gene polymorphisms may contribute to the extent of cerebrovascular disease risk. http://www.doiserbia.nb.rs/img/doi/0354-4664/2007/0354-46640704303S.pdfApoBischemic cerebrovascular diseasegenepolymorphismhuman populationSerbia
collection DOAJ
language English
format Article
sources DOAJ
author Stanković Aleksandra
Stanković Sanja
Jovanović-Marković Zagorka
Živković Maja
Đurić Tamara
Glišić-Milosavljević Sanja
Alavantić D.
spellingShingle Stanković Aleksandra
Stanković Sanja
Jovanović-Marković Zagorka
Živković Maja
Đurić Tamara
Glišić-Milosavljević Sanja
Alavantić D.
Apolipoprotein B gene polymorphisms in patients from Serbia with ischemic cerebrovascular disease
Archives of Biological Sciences
ApoB
ischemic cerebrovascular disease
gene
polymorphism
human population
Serbia
author_facet Stanković Aleksandra
Stanković Sanja
Jovanović-Marković Zagorka
Živković Maja
Đurić Tamara
Glišić-Milosavljević Sanja
Alavantić D.
author_sort Stanković Aleksandra
title Apolipoprotein B gene polymorphisms in patients from Serbia with ischemic cerebrovascular disease
title_short Apolipoprotein B gene polymorphisms in patients from Serbia with ischemic cerebrovascular disease
title_full Apolipoprotein B gene polymorphisms in patients from Serbia with ischemic cerebrovascular disease
title_fullStr Apolipoprotein B gene polymorphisms in patients from Serbia with ischemic cerebrovascular disease
title_full_unstemmed Apolipoprotein B gene polymorphisms in patients from Serbia with ischemic cerebrovascular disease
title_sort apolipoprotein b gene polymorphisms in patients from serbia with ischemic cerebrovascular disease
publisher University of Belgrade, University of Novi Sad
series Archives of Biological Sciences
issn 0354-4664
publishDate 2007-01-01
description The plasma concentration of apoB has recently been reported to be the best lipid predictor of coronary heart disease. The possible associations of genetic markers in the apolipoprotein B gene (XbaI, EcoRI, MspI, Ins/Del, and 4311 A/G polymorphisms) were evaluated in patients with ischemic cerebrovascular disease (ICVD) and controls of equivalent BMI. The odds ratio for ICVD in the X+X+ genotype was 2.22, 95% CI 1.24-3.96 (P<0.05), while that for ICVD in the Ins/Ins genotype was 2.82, 95% CI 1.57-5.06 (P<0.05). The patients had significantly higher frequency of the 4311A allele compared to the controls (P<0.01). Our results support the assumption that apoB gene polymorphisms may contribute to the extent of cerebrovascular disease risk.
topic ApoB
ischemic cerebrovascular disease
gene
polymorphism
human population
Serbia
url http://www.doiserbia.nb.rs/img/doi/0354-4664/2007/0354-46640704303S.pdf
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