Gewählte Publikation:
SHR
Neuro
Krebs
Kardio
Lipid
Stoffw
Microb
Kleber, ME; Grammer, TB; Renner, W; März, W.
Effect of the rs2259816 polymorphism in the HNF1A gene on circulating levels of c-reactive protein and coronary artery disease (the ludwigshafen risk and cardiovascular health study).
BMC Med Genet. 2010; 11(4):157-157
Doi: 10.1186/1471-2350-11-157
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
- Führende Autor*innen der Med Uni Graz
-
März Winfried
- Co-Autor*innen der Med Uni Graz
-
Renner Wilfried
- Altmetrics:
- Dimensions Citations:
- Plum Analytics:
- Scite (citation analytics):
- Abstract:
-
C-reactive protein is a well established marker of inflammation and has been used to predict future cardiovascular disease. It is still controversial if it plays an active role in the development of cardiovascular disease. Recently, polymorphisms in the gene for HNF1α have been linked to the levels of C-reactive protein and coronary artery disease.
We investigated the association of the rs2259816 polymorphism in the HNF1A gene with the circulating level of C-reactive protein and the hazard of coronary artery disease in the LURIC Study cohort.
Compared to CC homozygotes, the level of C-reactive protein was decreased in carriers of at least one A-allele. Each A-allele decreased CRP by approximately 15%. The odds ratio for coronary artery disease was only very slightly increased in carriers of the A-allele and this association did not reach statistical significance.
In the LURIC Study cohort the A-allele of rs2259816 is associated with decreased CRP but not with coronary artery disease.
- Find related publications in this database (using NLM MeSH Indexing)
-
C-Reactive Protein - metabolism
-
Cohort Studies -
-
Coronary Artery Disease - blood
-
Coronary Artery Disease - epidemiology
-
Coronary Artery Disease - genetics
-
Genotype -
-
Genotype -
-
Hepatocyte Nuclear Factor 1-alpha - genetics
-
Humans -
-
Polymorphism, Genetic -
-
Risk Factors -