3 results match your criteria: "G. Salvatore University Magna Graecia of Catanzaro[Affiliation]"
Eur J Intern Med
May 2015
Department of Experimental and Clinical Medicine, "G. Salvatore" University "Magna Graecia" of Catanzaro, Catanzaro, Italy.
Background: Cardiovascular disease represents one of the most important extra-articular causes of morbidity and mortality in patients with rheumatoid arthritis (RA). Evidences showed that several cardiac structures can be affected during the course of the disease as well as abnormalities of left ventricular diastolic filling. Contrasting data are available about left ventricular mass (LVM) involvement in patients asymptomatic for cardiovascular disease.
View Article and Find Full Text PDFDiabetes Care
January 2012
Department of Experimental and Clinical Medicine, “G. Salvatore” University Magna Græcia of Catanzaro, Catanzaro, Italy.
Objective: Subjects who are normal glucose tolerant (NGT) are considered at low risk, even if a plasma glucose value ≥155 mg/dL for the 1-h postload plasma glucose during an oral glucose tolerance test (OGTT) is able to identify NGT subjects at high risk for type 2 diabetes and subclinical organ damage. Hyperuricemia is associated with several risk factors for cardiovascular diseases such as hypertension, insulin resistance, and diabetes. However, it is unknown whether uric acid (UA) is able to affect 1-h postload plasma glucose in hypertensive NGT subjects.
View Article and Find Full Text PDFJ Clin Endocrinol Metab
July 2004
Department of Experimental and Clinical Medicine, G. Salvatore University Magna Graecia of Catanzaro, Policlinico Mater Domini-Via Tommaso Campanella, 88100 Catanzaro, Italy.
Some cardiovascular risk factors, such as hypertension and insulin resistance, are associated with endothelial dysfunction. Insulin regulates both in vitro and in vivo expression of endothelial nitric oxide synthase (eNOS) via a pathway involving insulin receptor substrate-1 (IRS-1) and phosphatidylinositol-3 kinase. Recently, we found that human endothelial cells obtained from carriers of the Arg(972) IRS-1 polymorphism exhibited reduced eNOS expression in response to chronic exposure to insulin.
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