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Apolipoprotein E Polymorphism in Hemodialyzed Patients and Healthy Controls

Jaroslav A. Hubacek1, 2, 3 Contact Information, Silvie Bloudickova1, Ruzena Kubinova4, Hynek Pikhart5, Ondrej Viklicky1 and Martin Bobak5

(1)  Institute for Clinical and Experimental Medicine, CEM, Laboratory for Molecular Genetics, Videnska 1958/9, Prague 4, 14021, Czech Republic
(2)  Third Internal Department, First Medical Faculty, Charles University, Prague, Czech Republic
(3)  Cardiovascular Research Centre, Prague, Czech Republic
(4)  National Institute of Public Health, Prague, Czech Republic
(5)  Department of Epidemiology and Public Health, University College London, London, UK

Received: 3 November 2008  Accepted: 9 June 2009  Published online: 30 June 2009

Abstract  A possible association between end-stage renal disease (ESRD) and apolipoprotein E (APOE) polymorphism was found in some but not all studies. We have analyzed the APOE genotypes in 995 hemodialyzed patients (cases) and a sample of 6242 healthy individuals (controls) in the Czech Republic. There was a statistically significant difference in the frequency of APOE alleles between cases and controls, with more carriers of the APOE2 allele in ESRD patients (15.9%) than in controls (12.2%) (P = 0.005). The odds ratio of ESRD for the APOE2 allele, compared with APOE3E3 homozygotes, was 1.37 (95% confidence interval 1.13–1.67). The strength of the association increased with the time spent on hemodialysis: the odds ratio of all-cause ESRD in patients dialyzed for eight or more years was 1.27 (0.94–1.71), for 1–8 years 1.41 (1.09–1.81), and less than 1 year (nonsurvivors) 1.94 (0.88–4.18). This study suggests that the APOE2 allele is a possible genetic risk factor for all-cause ESRD in Caucasians.

Keywords  Apolipoprotein E - End-stage renal disease - Polymorphism

This study is conducted for the MIA group.

Contact Information Jaroslav A. Hubacek
Email: jahb@ikem.cz
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