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Apolipoprotein E Polymorphism in Hemodialyzed Patients and Healthy Controls
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Apolipoprotein E Polymorphism in Hemodialyzed Patients and Healthy Controls
Jaroslav A. Hubacek1, 2, 3 , 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.
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