Abstract

ObjectiveMetabolic syndrome (MetS) or prediabetes is a complex disorder that is defined by a clustering of cardiometabolic risk factors, including obesity, hypertriglyceridemia, reduced high-density lipoprotein (HDL) cholesterol, hypertension, and insulin resistance. Among cardiometabolic risk factors, central obesity plays a key role in the development of MetS through alterations in the secretion of adipokines and interacts with other MetS risk factors to unfavorably influence overall cardiometabolic risk. Obesity has grasped epidemic proportions in Asia, which has the highest number of people with diabetes in the world. But, the importance of central obesity in the clustering of all four MetS risk factors or vice versa in predicting severity of MetS has not yet been investigated in Asian population. Therefore, the present study examined the influence of central obesity on circulating levels of adipokines through its interaction with the clustering of cardiometabolic risk factors of MetS including hyperglycemia, hypertriglyceridemia, dyslipidemia and hypertension in Hong Kong Chinese adults.SubjectsBlood samples from 83 Hong Kong Chinese adults, who were previously screened for MetS according to the guideline of the United States National Cholesterol Education Program Expert Panel Adult Treatment Panel III criteria were selected. Insulin and adipokines, including visfatin, chemerin, plasminogen activator inhibitor-1 (PAI-1), resistin, C-C motif chemokine ligand 2 (CCL-2), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10), tumour necrosis factor-α (TNF-α), leptin and adiponectin were assessed.ResultsThe interacting effect of central obesity with all of the other four MetS risk factors increased the proinflammatory status of adipokines (TNF-α, leptin) and decreased the anti-inflammatory status of adipokine (adiponectin).ConclusionOur results indicate that the inflammatory status of MetS may be more severe in the presence of central obesity. Adipokines, as biomarkers for pathophysiological changes, may help to improve early patient identification and to predict MetS-associated morbidity and mortality.

Highlights

  • Metabolic syndrome (MetS) is a complex disorder that is defined by the clustering of cardiometabolic risk factors, including obesity, hypertriglyceridemia, reduced high-density lipoprotein (HDL) cholesterol, hypertension, and insulin resistance that together, culminate in an increased risk of type 2 diabetes mellitus (T2D) and cardiovascular disease (CVD) [1]

  • Our results indicate that the inflammatory status of MetS may be more severe in the presence of central obesity

  • Circulatory levels of tumour necrosis factor-α (TNF-α) and leptin exacerbated, and adiponectin decreased in people with central obesity and the clustering of other 4 MetS risk factors

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Summary

Introduction

Metabolic syndrome (MetS) is a complex disorder that is defined by the clustering of cardiometabolic risk factors, including obesity, hypertriglyceridemia, reduced high-density lipoprotein (HDL) cholesterol, hypertension, and insulin resistance that together, culminate in an increased risk of type 2 diabetes mellitus (T2D) and cardiovascular disease (CVD) [1]. In particular central obesity, plays an important role in the development of MetS [2] and is associated with an increased risk of cardiovascular disorders, T2D and certain cancers [3]. Central obesity has been associated with an increased risk of CVD in subjects with or without MetS [5]. Intra-abdominal adiposity interacts with other MetS risk factors to unfavorably influence overall cardiometabolic risk. Intra-abdominal adiposity has been allied with adverse changes in lipid profile in older people before and after adjustment for overall adiposity [7]

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