Endothelial Dysfunction Is Associated with Decreased Nitric Oxide Bioavailability in Dysglycaemic Subjects and First-Degree Relatives of Type 2 Diabetic Patients.
Ignatios IkonomidisGeorge PavlidisMaria TsoumaniFoteini KousathanaKonstantinos KatogiannisDamianos TsilivarakisJohn ThymisAikaterini KountouriEmmanouil KorakasLoukia PlioutaAthanasios RaptisJohn ParissisIoanna AndreadouVaia LambadiariPublished in: Journal of clinical medicine (2022)
Oxidative stress plays an important role in the pathogenesis of diabetes. We investigated oxidative stress and nitrite/nitrate concentrations at baseline and during postprandial hyperglycaemia in 40 first-degree relatives (FDRs) of diabetic patients with normal oral glucose tolerance test (OGTT) results, 40 subjects with abnormal OGTT results (dysglycaemic) and 20 subjects with normal OGTT results (normoglycaemic). Malondialdehyde (MDA), protein carbonyls (PCs), nitrite/nitrate plasma levels, the perfused boundary region (PBR-Glycocheck) of the sublingual microvessels, a marker of glycocalyx integrity, coronary flow reserve (CFR) and left ventricular global longitudinal strain (GLS) were assessed at 0 and 120 min of the OGTT. Insulin sensitivity was evaluated using Matsuda and the insulin sensitivity index (ISI). In all subjects, there were no significant changes in MDA or PC after the OGTT ( p > 0.05). Compared with normoglycaemic subjects, FDRs and dysglycaemic subjects had significantly decreased nitrite/nitrate levels (-3% vs. -24% vs. -30%, respectively), an increased PBR and reduced CFR and GLS at 120 min ( p < 0.05). The percent reduction in nitrite/nitrate was associated with abnormal Matsuda and ISI results, reversely related with the percent increase in PBR (r = -0.60) and positively related with the percent decrease in CFR (r = 0.39) and GLS (r = 0.48) ( p < 0.05). Insulin resistance is associated with reduced nitric oxide bioavailability and coronary and myocardial dysfunction in FDRs and dysglycaemic subjects.
Keyphrases
- nitric oxide
- oxidative stress
- nitric oxide synthase
- left ventricular
- type diabetes
- hydrogen peroxide
- insulin resistance
- coronary artery disease
- cardiovascular disease
- coronary artery
- heart failure
- blood pressure
- acute myocardial infarction
- hypertrophic cardiomyopathy
- high fat diet
- skeletal muscle
- metabolic syndrome
- signaling pathway
- mitral valve
- glycemic control
- acute coronary syndrome
- percutaneous coronary intervention
- atomic force microscopy
- pi k akt