Abstract

BackgroundMetabolic syndrome (MetS) contains a cluster of cardiovascular risk factors. People with MetS are more susceptible to cardiovascular disease, diabetes mellitus, and cancer. Endothelin-1 (ET-1) and matrix metallopeptidase-9 (MMP-9) have been implicated in the development of cardiovascular diseases, diabetes mellitus and cancers. This cross-sectional study aimed to examine the association of ET-1 and MMP-9 with MetS in middle-aged and older Hong Kong Chinese adults.Methods149 adults aged 50 to 92 (n = 75 for non-MetS group and n = 74 for MetS group) were examined. All subjects were screened for MetS according to the diagnostic guideline of the United States National Cholesterol Education Program (NCEP) Expert Panel Adult Treatment Panel (ATP) III criteria. Serum levels of ET-1 and MMP-9 were measured. Independent t test was used to detect differences between non-MetS and MetS groups and between subjects with or without certain metabolic abnormality. The association of the serum concentration of MMP-9 and ET-1 with MetS parameters were examined by Pearson’s correlation analysis.ResultsSerum level of ET-1 is higher in MetS-positive subjects and in subjects with high blood pressure, elevated fasting blood glucose, and central obesity. The serum concentration of MMP-9 is higher in subjects positively diagnosed with MetS and subjects with high blood pressure, elevated fasting blood glucose, low blood high-density lipoprotein-cholesterol (HDL-C), high blood triglycerides, and central obesity. Correlation analyses revealed that serum concentration of ET-1 is positively correlated to systolic blood pressure, waist circumference, fasting blood glucose, and age whereas it is negatively correlated to HDL-C. MMP-9 is positively correlated to systolic blood pressure, waist circumference, fasting blood glucose, and age whereas it is negatively correlated to HDL-C.ConclusionSerum ET-1 is higher in subjects with hypertension, hyperglycemia, central obesity or MetS. Serum MMP-9 is higher in subjects diagnosed with MetS or having either one of the MetS parameters. Both circulating levels of ET-1 and MMP-9 are correlated to systolic blood pressure, waist circumference, fasting blood glucose, HDL-C, and age. Further research is needed to fully dissect the role of ET-1 and MMP-9 in the development of cancers, diabetes and cardiovascular disease in relation to MetS.

Highlights

  • Metabolic syndrome (MetS) contains a cluster of cardiovascular risk factors

  • Elevated plasma ET-1 level is observed in patients of diabetes mellitus [9] and cardiovascular diseases [11] while ET-1 has been suggested to be related to the promotion of cancer development by modulating mitosis, angiogenesis and apoptosis [13]

  • Individuals diagnosed with MetS have more than two of following characteristics: (1) central obesity, (2) hypertension, (3) elevated blood glucose, (4) elevated plasma triglycerides, and (5) low level of high-density lipoprotein-cholesterol (HDL-C; level equals or is less than 40 mg/dL for male and 50 mg/dL for female) are regarded as MetS positive

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Summary

Introduction

Metabolic syndrome (MetS) contains a cluster of cardiovascular risk factors. Endothelin-1 (ET-1) and matrix metallopeptidase-9 (MMP-9) have been implicated in the development of cardiovascular diseases, diabetes mellitus and cancers. This cross-sectional study aimed to examine the association of ET-1 and MMP-9 with MetS in middle-aged and older Hong Kong Chinese adults. Metabolic syndrome (MetS) is regarded as a sub-health status that contains a clustering of cardiovascular risk factors, including high blood pressure, central obesity, Yu et al Diabetol Metab Syndr (2015) 7:111. Its abundance is highly increased during pathological conditions due to the stimulated production in different types of cell including endothelial cells, cardiac myocytes, smooth muscle cells and inflammatory cells [11, 17, 18]. Elevated plasma ET-1 level is observed in patients of diabetes mellitus [9] and cardiovascular diseases [11] while ET-1 has been suggested to be related to the promotion of cancer development by modulating mitosis, angiogenesis and apoptosis [13]

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