The plasminogen activator inhibitor-1 (PAI-1) promoter haplotype is related to PAI-1 plasma concentrations in lean individuals

Elevated plasminogen activator inhibitor-1 (PAI-1) concentrations are associated with cardiovascular diseases. PAI-1 antigen levels are influenced by environmental factors such as body mass index (BMI), and by genetic factors. The PAI-1 promoter of the PAI-1 gene contains two common polymorphisms (−...

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Veröffentlicht in:Atherosclerosis 2005-08, Vol.181 (2), p.275-284
Hauptverfasser: Verschuur, Maartje, Jellema, Annemarie, Bladbjerg, Else M., M. Feskens, Edith J., Mensink, Ronald P., Møller, Lars, Vos, Hans L., de Maat, Moniek P.M.
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Sprache:eng
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Zusammenfassung:Elevated plasminogen activator inhibitor-1 (PAI-1) concentrations are associated with cardiovascular diseases. PAI-1 antigen levels are influenced by environmental factors such as body mass index (BMI), and by genetic factors. The PAI-1 promoter of the PAI-1 gene contains two common polymorphisms (−844A/G and −675(4G/5G)) and the 4G allele of the −675(4G/5G) variation has been associated with elevated PAI-1 concentrations and on some occasions with an increased risk of cardiovascular disease. The aim of our study was to investigate the effect of the PAI-1 promoter haplotype on PAI-1 concentrations and to determine the role of BMI. The association between the PAI-1 promoter haplotype and PAI-1 antigen levels was investigated in two independent populations, each including 600 healthy Caucasians. Furthermore, to assess the effect of the PAI-1 promoter haplotype on PAI-1 promoter activity, in vitro reporter gene assays were performed in HepG2 and BAEC cells. We observed significantly higher PAI-1 concentrations in A-4G homozygotes than in G-5G carriers in lean subjects (BMI in the lowest quartile). In these lean subjects, the PAI-1 concentrations in A-4G/G-5G heterozygotes were reduced to 60–75%, and the concentrations in G-5G homozygotes to 45–55%, compared to the PAI-1 concentrations of A-4G homozygotes ( p < 0.01). PAI-1 concentrations increased approximately four-fold from the lowest to the highest BMI quartile ( p < 0.01). The reporter gene assays did not support a direct effect of the PAI-1 promoter haplotype on promoter activity in HepG2 or BEAC cells. Our study suggests that the PAI-1 promoter haplotype and BMI affect PAI-1 concentrations and that BMI is a stronger determinant than PAI-1 promoter variation.
ISSN:0021-9150
1879-1484
DOI:10.1016/j.atherosclerosis.2005.01.036