“…Moreover, the pharmacological inhibition of FABP4 also significantly protected against atherosclerotic plaque formation in the ApoE-deficient animal model of atherosclerosis, suggesting that the pharmacological inhibition of FABP4 might have beneficial effects against CVD (Furuhashi et al 2007). In humans, FABP4 has been related to subclinical coronary atherosclerosis in type 2 diabetes mellitus subjects (Bagheri et al 2010), and circulating FABP4 levels are also associated with increased carotid intima-media thickness, ischaemic stroke, coronary atherosclerotic burden and the number of stenotic coronary arteries , Rhee et al 2009, Miyoshi et al 2010, Bao et al 2011, Doi et al 2011, Holm et al 2011, Tso et al 2011, Huang et al 2013. Recently, FABP4 has been proposed as a prognostic biomarker in patients with acute coronary syndrome (Reiser et al 2015).…”