APOE polymorphism and its effect on plasma C-reactive protein levels in a large general population sample

. 2010 Mar ; 71 (3) : 304-8. [epub] 20100125

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid20074603

Grantová podpora
G0100222 Medical Research Council - United Kingdom
064947/Z/01/Z Wellcome Trust - United Kingdom
G0902037 Medical Research Council - United Kingdom
R01 AG023522 NIA NIH HHS - United States
R01 AG023522-05 NIA NIH HHS - United States
R01 AG013196 NIA NIH HHS - United States
Wellcome Trust - United Kingdom
081081/Z/06/Z Wellcome Trust - United Kingdom
RG/07/008/23674 British Heart Foundation - United Kingdom
G8802774 Medical Research Council - United Kingdom
1R01 AG23522-01 NIA NIH HHS - United States
G19/35 Medical Research Council - United Kingdom

Odkazy

PubMed 20074603
PubMed Central PMC2837141
DOI 10.1016/j.humimm.2010.01.008
PII: S0198-8859(10)00009-1
Knihovny.cz E-zdroje

The published data remain inconsistent on association between apolipoprotein E (APOE) gene variations and plasma levels of C-reactive protein (CRP), mainly because of low statistical power of previous studies. To clarify this question, we analyzed data from large population sample of randomly selected individuals from seven Czech towns (2,886 males and 3,344 females, the HAPIEE [Health, Alcohol, and Psychosocial factors In Eastern Europe] study). In both males and females, the lowest levels of plasma hsCRP were observed in the carriers of the APOE epsilon 4 epsilon 4 and epsilon 4 epsilon 3 genotypes. The median (interquartile range, IQR) concentration of hsCRP in carriers of the most common APOE epsilon 3 epsilon 3 genotype (two-thirds of participants) was 1.13 mg/l (IQR, 0.56-2.33) in men and 1.23 mg/l (IQR, 0.61-2.65) in women, compared with 0.72 mg/l (IQR, 0.61-0.86) in male and 0.72 mg/l (IQR, 0.61-0.85) in female carriers of APOE epsilon 4 epsilon 3/epsilon 4 epsilon 4 genotypes; the differences were statistically significant (p < 0.001). The association between APOE and CRP was not materially affected by adjustment for age, sex, history of cardiovascular disease, or cardiovascular risk factors. This study, the largest to date, provides robust evidence of an association between plasma hsCRP and the APOE genotype, an association not explained by history of cardiovascular disease nor its risk factors.

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