Literature DB >> 12668909

The metabolic syndrome: targeting dyslipidaemia to reduce coronary risk.

Henry N Ginsberg1, Anton F H Stalenhoef.   

Abstract

The metabolic syndrome is a complex constellation of disorders, each one a significant risk factor for the development of cardiovascular disease (CVD). The increasing prevalence of this condition is a major concern for healthcare providers both in Europe and North America. The concern surrounding the prevalence of the metabolic syndrome is reflected in the recently published National Cholesterol Education Program Adult Treatment Panel III guidelines. Although complex in nature, the individual components of the metabolic syndrome appear to be linked by the presence of insulin resistance. Concurrently treating the underlying insulin resistance along with the complex array of other disorders should form the core of any management strategy. Treatment of atherogenic dyslipidaemia should be a major aim, since it is associated with a significant risk of CVD. While lifestyle modifications form the cornerstone of any dyslipidaemia management strategy, many patients require the addition of lipid-modifying drugs. Several agents are available for the treatment of lipid abnormalities, including fibrates, bile acid sequestrants, niacin and hydroxymethyl glutaryl coenzyme A reductase inhibitors (statins). Of these, statins should be used as the first treatment option in the majority of patients because they are efficacious for reducing low-density lipoprotein cholesterol, are effective across the lipid profile and are well tolerated in the majority of cases. Furthermore, the American Diabetes Association (ADA) recommends statins as first-line pharmacological treatment of dyslipidaemia in patients with diabetes mellitus. This review discusses the diagnosis and management of the metabolic syndrome and examines the potential of future treatment options.

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Year:  2003        PMID: 12668909     DOI: 10.1097/01.hjr.0000060840.46106.ea

Source DB:  PubMed          Journal:  J Cardiovasc Risk        ISSN: 1350-6277


  17 in total

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2.  Sex-specific association of the SPTY2D1 rs7934205 polymorphism and serum lipid levels.

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Review 3.  Interaction of gut microbiota with bile acid metabolism and its influence on disease states.

Authors:  Alexander Khoruts; Michael J Sadowsky; Christopher Staley; Alexa R Weingarden
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4.  Mechanisms of lipase maturation.

Authors:  Mark H Doolittle; Miklós Péterfy
Journal:  Clin Lipidol       Date:  2010-02-01

5.  Effects of macrophage-specific adiponectin expression on lipid metabolism in vivo.

Authors:  Nanlan Luo; Xiangdong Wang; B Hong Chung; Mi-Hye Lee; Richard L Klein; W Timothy Garvey; Yuchang Fu
Journal:  Am J Physiol Endocrinol Metab       Date:  2011-04-19       Impact factor: 4.310

Review 6.  Evidence-based and heuristic approaches for customization of care in cardiometabolic syndrome after spinal cord injury.

Authors:  Mark S Nash; Rachel E Cowan; Jochen Kressler
Journal:  J Spinal Cord Med       Date:  2012-09       Impact factor: 1.985

7.  Angiotensin II Blockade and Total Cardiovascular Risk : Beyond Blood Pressure Reduction.

Authors:  Francesco Cipollone; Sara Di Fabio; Marco Bucci; Giancarlo Cicolini; Andrea Mezzetti
Journal:  High Blood Press Cardiovasc Prev       Date:  2013-01-22

Review 8.  New drugs for type 2 diabetes mellitus: what is their place in therapy?

Authors:  Andrew J Krentz; Mayank B Patel; Clifford J Bailey
Journal:  Drugs       Date:  2008       Impact factor: 9.546

9.  Lipoprotein kinetics in the metabolic syndrome: pathophysiological and therapeutic lessons from stable isotope studies.

Authors:  Dick C Chan; P Hugh R Barrett; Gerald F Watts
Journal:  Clin Biochem Rev       Date:  2004-02

10.  Effects of rosuvastatin and atorvastatin on LDL and HDL particle concentrations in patients with metabolic syndrome: a randomized, double-blind, controlled study.

Authors:  Robert S Rosenson; James D Otvos; Judith Hsia
Journal:  Diabetes Care       Date:  2009-03-05       Impact factor: 19.112

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