PPAR gamma expression levels during development of heart failure in patients with coronary artery disease after coronary artery bypass-grafting

7Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Genetic research has elucidated molecular mechanisms of heart failure (HF). Peroxisome proliferator-activated receptors (PPARs) seem to be important in etiology of HF. The aim of study was to find the correlation between PPAR γ expression during development of HF in patients and coronary artery disease (CAD) after coronary artery bypass-grafting (CABG). Methods and Results. We followed up 157 patients (mean age 63) with CAD without clinical, laboratory, or echo parameters of HF who underwent CABG. Clinical and laboratory status were assessed before CABG and at 1, 12, and 24 months. During CABG slices of aorta (Ao) and LV were collected for genetic research. HF was defined as LVEF <40% or NT-proBNP >400 pg/mL or 6MWT <400 m. Patients were divided into 2 groups: with and without HF. PPAR γ expression in Ao and LV was not increased in both groups at 2-year follow-up. Sensitivity of PPAR γ expression in Ao above 1.1075 in detection of HF was 20.5% (AUC 0.531, 95% CI 0.442-0.619). Positive predictive value (Ppv) was 85.7%. Sensitivity and specificity of PPAR γ expression in the LV in detection of HF were 58% and 92.9%, respectively (AUC 0.540, 95% CI 0.452-0.626). Ppv was 73.2%. Conclusion. PPAR γ expression in Ao and LV was comparable and should not be used as predictive factor for development of HF in patients with CAD after CABG.

Cite

CITATION STYLE

APA

Wojtkowska, I., Tysarowski, A., Seliga, K., Siedlecki, J. A., Juraszyński, Z., Marona, M., … Stępińska, J. (2014). PPAR gamma expression levels during development of heart failure in patients with coronary artery disease after coronary artery bypass-grafting. PPAR Research, 2014. https://doi.org/10.1155/2014/242790

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