Coronary risk biomarkers in centrally obese patients with and without metabolic syndrome

• Main Author: Hanis Saimin (Author)
• Format: Thesis Book
• Language: English
• Published: Sungai Buloh, Selangor Universiti Teknologi MARA. Faculty of Medicine 2016
• Subjects: Biomarkers > adverse effects; metabolic syndrome
• Online Access: Click Here to View Status and Holdings.

 Metabolic syndrome (MS) represents a cluster of risk factors consisting of central obesity, atherogenic dyslipidaemia, hypertension and insulin resistant which increases coronary heart disease risk. Central obesity was postulated to be the underlying mechanism of metabolic syndrome. This present study aims to determine the relationship between coronary risk biomarkers, abdominal fat volume indices and carotid intima-media thickness (IMT) in drug naïve MS, central obesity without MS (COBXMS) and normal lean controls (NC), and between MS glycaemic subgroups. A cross sectional study involving 498 subjects (163 males and 355 females, age (mean+SD): 47.4+8.3 years) categorized into MS, COBXMS and NC. MS subjects were subdivided according to glycaemic status: diabetes mellitus (MDSM), impaired fasting glucose (MSIFG) and normoglycaemic (MSNG). Both MS and COBXMS had lower adiponectin and higher coronary risk biomarkers, abdominal fat volume indices and carotid IMT compared to NC; but these biomarkers were similar between MS and COBXMS. Similarly, MS glycaemic subgroups showed no differences (p>0.05) in these biomarkers. Waist circumference, blood pressure and subcutaneous fat volume were the independent variables affecting coronary risk biomarkers in all subjects after correcting for the various confounding factors. Among the MS glycaemic subgroups, waist circumference and blood pressure remained to be the independent variable. Central obesity without MS has reduced atheroprotective adipokine and enhanced prothrombotic and inflammation status comparable to MS, suggesting increased coronary risk in centrally obese subjects even in the absence of metabolic syndrome.