Adiponectin and E-selectin concentrations in relation to inflammation in obese type 2 diabetic patients with coronary heart disease(s)
dc.Affiliation | October University for modern sciences and Arts (MSA) | |
dc.contributor.author | El-Mesallamy H.O. | |
dc.contributor.author | Hamdy N.M. | |
dc.contributor.author | Salman T.M. | |
dc.contributor.author | Mahmoud S. | |
dc.contributor.other | Biochemistry Department | |
dc.contributor.other | Faculty of Pharmacy | |
dc.contributor.other | Ain Shams University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Biochemistry Department | |
dc.contributor.other | Faculty of Pharmacy | |
dc.contributor.other | AL-Azhar University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Modern Sciences and Arts University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt | |
dc.date.accessioned | 2020-01-25T19:58:30Z | |
dc.date.available | 2020-01-25T19:58:30Z | |
dc.date.issued | 2011 | |
dc.description | Scopus | |
dc.description.abstract | Aim. Adipose tissue is now regarded as a source of proinflammatory mediators which may contribute to vascular injury, insulin resistance (IR), and atherogenesis, however, some of them have a protective role against vascular inflammation and/or IR; namely adiponectin and nitric oxide (NO). Adiponectin is a fat derived hormone, which enhances insulin sensitivity. In experimental studies adiponectin was shown to have anti-atherogenic properties by suppressing endothelial expression of adhesion molecules as endothelial-selectin (E-selectin) and inflammatory cytokines as high-sensitivity C-reactive protein (hsCRP), interleukin-1? (IL-1?), and monocyte chemotactic protein-1 (MCP-1). Therefore, the aim of the study was to evaluate plasma adiponectin, E-selectin, hsCRP, IL-1?, and MCP-1 concentrations in obese patients with and without coronary heart disease (CHD) having type 2 diabetes mellitus (DM) and evaluation of their relationship with selected anthropometric, biochemical, and clinical parameters. Methods. The study group consisted of (N.=70) males, 20 of which served as healthy non-obese controls (group I) (mean age 38.53.7 years; mean BMI 28 1.2 kg/m2). Patients enrolled in the study were classified into the following groups: type 2 DM obese subjects without CHD (group II) (N.=25) (mean age 42.23 years; mean BMI 32.11.4 kg/m2) and type 2 DM obese subjects with CHD (group III) (N.=25) (mean age 40.63 years; mean BMI 31.51.2 kg/m 2). Glucose and insulin estimation was performed and insulin resistance index (HOMA-IR) was calculated. In the fasting state, the plasma HbA1c, adiponectin, E-selectin, in comparison to hsCRP, IL-1?, MCP-1, and lipid parameters were estimated. Results. FBG, HbA 1c%, lipids, insulin, MDA, NO, hsCRP, IL-?, MCP-1, Adiponectin as well as E-selectin concentration were significantly different in patients with type 2 DM and CHD in comparison to patients without CHD and moreover, the healthy control group (P=0.01). There was a significant negative correlation between adiponectin and E-selectin (r=-0.642; P=0.0001). Conclusion. Our study supports the hypothesis that decreased level of adipokine(s), together with increased oxidative stress, pro-inflammatory marker(s) as well as endothelial adhesion molecule(s) contributes to the complex process of atherosclerosis in type 2 diabetic obese patients that may lead eventually to CHD. | en_US |
dc.description.uri | https://www.scimagojr.com/journalsearch.php?q=26205&tip=sid&clean=0 | |
dc.identifier.doi | https://doi.org/ | |
dc.identifier.issn | 3911977 | |
dc.identifier.other | https://doi.org/ | |
dc.identifier.uri | https://t.ly/ge8g8 | |
dc.language.iso | English | en_US |
dc.relation.ispartofseries | Minerva Endocrinologica | |
dc.relation.ispartofseries | 36 | |
dc.subject | Adiponectin | en_US |
dc.subject | Coronary diseases | en_US |
dc.subject | Diabetes mellitus | en_US |
dc.subject | Obesity | en_US |
dc.subject | adiponectin | en_US |
dc.subject | C reactive protein | en_US |
dc.subject | endothelial leukocyte adhesion molecule 1 | en_US |
dc.subject | glucose | en_US |
dc.subject | hemoglobin A1c | en_US |
dc.subject | insulin | en_US |
dc.subject | interleukin 1beta | en_US |
dc.subject | lipid | en_US |
dc.subject | monocyte chemotactic protein 1 | en_US |
dc.subject | nitric oxide | en_US |
dc.subject | adipose tissue | en_US |
dc.subject | adult | en_US |
dc.subject | article | en_US |
dc.subject | atherogenesis | en_US |
dc.subject | atherosclerosis | en_US |
dc.subject | blood vessel injury | en_US |
dc.subject | controlled study | en_US |
dc.subject | diabetic obesity | en_US |
dc.subject | disease association | en_US |
dc.subject | glucose blood level | en_US |
dc.subject | human | en_US |
dc.subject | inflammation | en_US |
dc.subject | insulin resistance | en_US |
dc.subject | insulin sensitivity | en_US |
dc.subject | ischemic heart disease | en_US |
dc.subject | major clinical study | en_US |
dc.subject | male | en_US |
dc.subject | non insulin dependent diabetes mellitus | en_US |
dc.subject | oxidative stress | en_US |
dc.subject | vasculitis | en_US |
dc.subject | Adiponectin | en_US |
dc.subject | Adult | en_US |
dc.subject | Algorithms | en_US |
dc.subject | Biological Markers | en_US |
dc.subject | Body Mass Index | en_US |
dc.subject | C-Reactive Protein | en_US |
dc.subject | Case-Control Studies | en_US |
dc.subject | Chemokine CCL2 | en_US |
dc.subject | Coronary Disease | en_US |
dc.subject | Diabetes Mellitus, Type 2 | en_US |
dc.subject | E-Selectin | en_US |
dc.subject | Glucose Intolerance | en_US |
dc.subject | Humans | en_US |
dc.subject | Inflammation | en_US |
dc.subject | Insulin Resistance | en_US |
dc.subject | Interleukin-1beta | en_US |
dc.subject | Male | en_US |
dc.subject | Middle Aged | en_US |
dc.subject | Obesity | en_US |
dc.subject | Predictive Value of Tests | en_US |
dc.subject | Sensitivity and Specificity | en_US |
dc.title | Adiponectin and E-selectin concentrations in relation to inflammation in obese type 2 diabetic patients with coronary heart disease(s) | en_US |
dc.type | Article | en_US |
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dcterms.source | Scopus |
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