Apolipoprotein E polymorphism in hemodialyzed patients and healthy controls
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
Wellcome Trust - United Kingdom
081081
Wellcome Trust - United Kingdom
T32 NR007958
NINR NIH HHS - United States
PubMed
19565203
PubMed Central
PMC3951864
DOI
10.1007/s10528-009-9266-y
Knihovny.cz E-zdroje
- MeSH
- apolipoproteiny E genetika MeSH
- chronické selhání ledvin genetika terapie MeSH
- dialýza ledvin * MeSH
- genotyp MeSH
- lidé MeSH
- polymorfismus genetický * MeSH
- senioři MeSH
- studie případů a kontrol MeSH
- zdraví * MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- apolipoproteiny E MeSH
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.
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