Advanced Glycation End Products:Receptors for Advanced Glycation End Products Axis in Coronary Stent Restenosis: A Prospective Study. 2018

Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
Division of Cardiology, Department of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

This study was aimed to correlate the pre- and 6-month postpercutaneous coronary intervention (PCI) serum concentrations of advanced glycation end products (AGE), soluble receptors for advanced glycation end products (sRAGE), AGE/sRAGE ratio, and serum malondialdehyde (MDA) levels with in-stent restenosis (ISR) among patients receiving either a drug-eluting stent (DES) or a bare-metal stent (BMS).In-stent restenosis remains as an adverse outcome following PCI. Sixty consecutive nondiabetic, Caucasian male patients, diagnosed with a non-ST-elevation myocardial infarction who received either a DES or BMS via PCI, were enrolled. Baseline levels of serum AGE, sRAGE, AGE/sRAGE ratios, MDA, and angiographic parameters were determined at stenting and at 6 months. Patients with and without ISR at 6 months were compared on both baseline and 6-month biomarker levels and within stent types.The pre-PCI serum AGE levels and AGE/sRAGE ratios were higher in ISR patients compared with non-ISR patients, while the pre-PCI and post-PCI serum sRAGE levels were lower in ISR patients compared with non-ISR patients. The pre and post-PCI levels of MDA were also higher in ISR patients. Comparing stent types, relative levels of MDA between those with and without ISR at the respective time points were similar, although changes between time points appeared type specific.Post-PCI ISR correlates with low serum values of sRAGE and high serum values of AGE, MDA, and AGE/sRAGE ratio which are present at stenting. The associations of baseline AGE, sRAGE, AGE/sRAGE, and MDA levels with ISR appear consistent between stent types.

UI MeSH Term Description Entries

Related Publications

Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
February 2005, Yonsei medical journal,
Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
November 2010, Clinical cardiology,
Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
April 2003, The American journal of pathology,
Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
January 2011, Coronary artery disease,
Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
October 2015, Journal of the Formosan Medical Association = Taiwan yi zhi,
Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
January 2011, Contributions to nephrology,
Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
April 2024, Gene,
Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
July 2011, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology,
Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
February 2001, Diabetologia,
Colin Pearce, and Naorin Islam, and Robyn Bryce, and Erick Donnell McNair
October 2019, Nutrition, metabolism, and cardiovascular diseases : NMCD,
Copied contents to your clipboard!