Association of the T+294C polymorphism in PPAR δ with low HDL cholesterol and coronary heart disease risk in women

48Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

Abstract

Background: The +T294C polymorphism in PPARδ represents a functional SNP affecting transcriptional activity of the PPARδ gene. To address whether this polymorphism is associated with the risk for coronary heart disease and/or plasma lipid levels in women, we studied a group of 967 female patients with hyperlipidaemia in the presence (n=453) or absence (n=514) of coronary heart disease. Methods: 967 female patients with or without coronary heart disease were genotyped using mutagenically separated polymerase chain reaction (MS-PCR). Statistical analysis was performed according to genotype with parameters of lipid metabolism as dependant variables. Results: A highly significant association between the rare C allele and lower plasma HDL concentrations was found in female subjects. The effect remained significant after correcting for multiparametric testing according to Bonferoni and was seen only in subjects with a BMI below the median. Moreover, a significant association of the C-allele with coronary heart disease and BMI was obtained. Regarding the entire group, trends towards higher VLDL and LDL levels were observed. Conclusions: Our data show for the first time that the PPARδ +T294C polymorphism is associated with lipid levels and coronary heart disease in women. However, the molecular mechanism of action remains to be elucidated. ©2006 Ivyspring International Publisher. All rights reserved.

Cite

CITATION STYLE

APA

Aberle, J., Hopfer, I., Beil, F. U., & Seedorf, U. (2006). Association of the T+294C polymorphism in PPAR δ with low HDL cholesterol and coronary heart disease risk in women. International Journal of Medical Sciences, 3(3), 108–111. https://doi.org/10.7150/ijms.3.108

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free