In this issue of Angiology, Rizk et al assess the association of adiponectin gene polymorphisms and, in particular, rs2241766 (þT45G) and rs1501299 (þG276T), with adiponectin levels and with the risk of acute coronary syndrome (ACS) in an Arabian cohort of Qatar. 1 Despite the study's limitations, such as the small sample size, the small proportion of females, and its cross-sectional nature, the authors concluded that only the single-nucleotide polymorphism (SNP) T45G (and not SNP G276T) was associated with ACS. Among the various genotypes of T45G, the GG carriers were associated with a higher risk of developing an ACS and having lower adiponectin levels. Some parameters were also addressed, such as diabetes mellitus (DM), number of blood vessels affected, and the ejection fraction status in ACS, but no association with the genotype distributions of T45G or G276T polymorphisms was found, except for EF with T45G. 1 This editorial considers some additional aspects of this topic.
Adiponectin and Cardiometabolic RiskAdiponectin is a 30-kDa protein secreted by mature adipocytes. It belongs to the soluble collagen superfamily, exerting structural homology with collagen VIII and X, complement factor C1q, and the tumor necrosis factor family. 2 It is composed of a carboxyl-terminal globular domain and an amino-terminal collagenous domain, a structure that facilitates the formation of multimers. These include low-molecular-weight trimers, middle-molecular-weight 6-mers, and high-molecular-weight (HMW) 18-mers. 2 Adiponectin seems to play a key role in the atherosclerotic process, since it inhibits monocyte adhesion to endothelial cells and suppresses lipid accumulation in human monocyte-derived macrophages, thus inhibiting macrophage-to-foam cell transformation. 3 Adiponectin also exerts anti-inflammatory and insulinsensitizing properties. 2,4 It acts through its receptors AdipoR1 and AdipoR2, in muscle and liver, respectively, stimulating adenosine monophosphate-activated protein kinase and the peroxisome proliferator-activated receptor-a pathways. 2,4 It increases fatty acid oxidation, reduces circulating free fatty acids, and prevents insulin resistance. 4