Despite their function for inflammatory host response and neural nociceptive excitability and traffic, some of the genes assessed from the CRPS patients like free fatty acid receptor 2 (FFAR2); interleukin receptor 1 antagonist (ILRN), interleukin 17-F (IL-17F); phospholipase A2, group IIA (PLA2G2); and NADPH oxidase (NOX1) have been associated with metabolic function such as glucose hemostasis, response to starvation, insulin resistance, lipid catabolic function, angiogenesis, blood pressure, and metabolic functions [79]. The gene discussed is IL17F; the disease is complex regional pain syndrome.