4.1 Article

Endocan is Related to Increased Cardiovascular Risk in Type 2 Diabetes Mellitus Patients

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Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/met.2023.0050

Keywords

atherosclerosis; cardiovascular risk; diabetes; endocan; obesity

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This study examined the relationship between serum endocan level and UKPDS risk engine score in type 2 diabetes patients. The results showed that endocan is an independent predictor for moderate and high estimated risks of cardiovascular disease in these patients.
Aim: Type 2 diabetes mellitus (T2D) patients have an increased risk for cardiovascular disease (CVD). Different algorithms are used for the CVD risk quantification and United Kingdom Prospective Diabetes Study (UKPDS) score was among the most validated. Endocan is a novel endothelial dysfunction marker. The aim was to explore the potential relationship between serum endocan level and UKPDS risk engine score [which enables calculation of the 10-year risk of nonfatal and fatal coronary heart disease (eCHD) and stroke] in T2D patients.Materials and Methods: The study included a cohort of 104 patients with T2D (of them 52.8% men), with median age 66 years and body mass index (BMI) = 30.7 kg/m(2). Patients were divided into: low (<15%), moderate (>= 15% and <30%), and high-risk UKPDS category (>= 30%).Results: In multivariable regression analysis (when adjusted for sex, BMI and/or hip circumference), endocan was the independent predictor for moderate and high estimated risks (nonfatal eCHD, fatal eCHD, and nonfatal stroke risk). In the Model for high nonfatal eCHD [areas under curve (AUC) = 0.895] and high fatal eCHD (AUC = 0.860) endocan indicated good clinical accuracy, and an excellent accuracy in discriminating patients with high risk for nonfatal stroke risk (AUC = 0.945).Conclusion: Endocan was the independent predictor for moderate and high estimated risks (i.e., nonfatal and fatal CHD and nonfatal stroke risk scores) in T2D patients. When included in models with sex and obesity indices endocan demonstrated good clinical accuracy in discriminating T2D patients with high risk for nonfatal and fatal eCHD and nonfatal stroke risk from those patients with low risk.

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