In recent years, the link between obesity, inflammation and atherosclerosis has attracted increasing interest. Recently, besides the classical inflammatory markers, the competitive nitric oxide synthase antagonist asymmetric dimethylarginine (ADMA) has been shown to be involved in the pathogenesis of atherosclerosis and cardiovascular diseases. Since obese people present a condition of chronic lowgrade inflammation and endothelial dysfunction, in the present study we quantified ADMA levels in uncomplicated obese women (with no clinical, cardiac or metabolic complications) and normal-weight control subjects. We investigated the relationship of ADMA with some anthropometric measurements, abdominal visceral and subcutaneous adipose tissue accumulation, and biochemical and proinflammatory factors of the subjects [interleukin-6 (IL-6), soluble IL-6 receptor (sIL-6R), IL6-R/IL-6 ratio, tumor necrosis factor alpha (TNFa), homocysteine (Hcy) and plasminogen activator inhibitor-l (PAl-I)]. ADMA and all the other pro-inflammatory parameters resulted.higher in obese patients than in healthy subjects. ADMA significantly correlated with Hey, PAl-I, TNFa and with sIL-6R/IL-6 ratio but not with other anthropometric and biochemical parameters. In a stepwise regression analysis ADMA correlated most closely with Hcy and TNFa. In conclusion, in our obese uncomplicated patients TNFa and Hcy emerged as strong predictors of ADMA which might be a potential mediator of the effects of different risk factors affecting the cardiovascular system.It is now well established that obesity is one of the most important independent risk factors for the development of atherosclerosis and cardiovascular diseases (CD) (1). Chronic immune-mediated inflammation, which involves adipokines, chemokines, cytokines and their receptors, and vascular endothelial cell dysfunction, characterized by a reduced bioavailability ofthe signaling molecule nitric oxide (NO), are both critically involved in the onset and progression of atherosclerosis (1-2).