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Understanding the Metabolic Syndrome Using a Biomedical Chemistry Profile

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2.3.1 Introduction For quite some time, it has been identified that high blood pressure, dyslipidemia [increased triglycerides and reduced high-density lipoprotein (HDL) cholesterol levels], impaired glucose homeostasis and abdominal obesity take place concurrently more than by random, supporting the existence of the metabolic syndrome (MetSyn). Additionally, hyperuricemia, a prothrombotic state, oxidative stress, chronic low grade inflammation, increased levels of apolipoprotein-B and small dense low density lipoprotein (LDL) cholesterol (contributing to atherogenic dyslipidemia), non-alcoholic fatty liver disease and/or non-alcoholic steatohepatitis, obstructive sleep apnea and/or polycystic ovarian disease (Fulop, 2006; Alberti, 2009; Roberts, 2009; Ma, 2012; Matsuda, 2013; Mule, 2014; Carson, 2015) are quite often present on the MetSyn, although not yet included in its current/actual definition. Taking this into consideration, it is not surprising that the MetSyn associates with an increased risk of type 2 diabetes mellitus (T2DM) and atherosclerotic cardiovascular disease (Fulop, 2006; Qiao, 2007; Carson, 2015).

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Metabolic Syndrome

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Citation

Pereira, C., Monteiro, R. & João Martins, M. (2015). 2.3 Understanding the Metabolic Syndrome Using a Biomedical Chemistry Profile. In Biomedical Chemistry: Current Trends and Developments (pp. 132-147). Warsaw, Poland: De Gruyter Open Poland. https://doi.org/10.1515/9783110468755-005

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De Gruyter

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Without CC licence

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