The link between abdominal obesity, metabolic syndrome and cardiovascular disease

Nutr Metab Cardiovasc Dis. 2007 May;17(4):319-26. doi: 10.1016/j.numecd.2006.07.005. Epub 2006 Nov 15.


Aim: The prevalence of metabolic syndrome has increased dramatically in recent years, and the cluster of metabolic abnormalities it encompasses results in increased cardiovascular morbidity and mortality. The role of abdominal (visceral) obesity and the underlying molecular and cellular mechanisms central to this association have been the subject of intensive research in recent times. The aim of this review is to correlate data in this area, highlighting the central role of excess visceral fat and its secreted adipokines, and to review existing and emerging therapies.

Data synthesis: Data were generated from a search of the PubMed database using the terms 'abdominal obesity', 'metabolic syndrome', 'insulin resistance', 'adipokines', 'interleukin-6 (IL-6)', 'adiponectin', 'tumour necrosis factor-alpha (TNF-alpha)' and 'cardiovascular disease'.

Conclusion: Metabolic syndrome is associated with a pro-inflammatory state, and the role of visceral obesity is thought to be central to this. Visceral obesity leads to alteration of the normal physiological balance of adipokines, insulin resistance, endothelial dysfunction and a pro-atherogenic state. In association with this, the presence of conventional cardiovascular risk factors such as hypertension, dyslipidaemia and smoking results in a significantly elevated cardiovascular and metabolic (cardiometabolic) risk. Better understanding of the molecular mechanisms central to this association has led to the development of potential therapeutic agents.

Publication types

  • Review

MeSH terms

  • Cardiovascular Diseases / etiology*
  • Cardiovascular Diseases / prevention & control
  • Fatty Acids, Nonesterified / blood
  • Humans
  • Inflammation / complications
  • Insulin Resistance
  • Interleukin-6 / blood
  • Intra-Abdominal Fat / physiology*
  • Metabolic Syndrome / complications*
  • Metabolic Syndrome / epidemiology
  • Obesity / complications*
  • Piperidines / therapeutic use
  • Pyrazoles / therapeutic use
  • Rimonabant
  • Risk Factors
  • Tumor Necrosis Factor-alpha / blood


  • Fatty Acids, Nonesterified
  • Interleukin-6
  • Piperidines
  • Pyrazoles
  • Tumor Necrosis Factor-alpha
  • Rimonabant