A study in human deep burn patients identified hsa-miR-200b as significantly down-regulated in denatured dermis compared to paired normal skin, with a 0.0253-fold change [Liang et al. DOI:10.1016/j.burns.2011.10.014]. A subsequent review confirmed its downregulation in human skin four days post-burn and further associated its decreased expression with burn-induced hypertrophic scar tissue and derived fibroblasts [Siu et al. DOI:10.1111/wrr.13100]. A study in a porcine model of cardiogenic shock demonstrated that the mir-200b is a hypoxia-sensitive circulating marker whose serum abundance is decreased following the induction of cardiogenic shock and is subsequently restored following mechanical ventricular unloading with pVAD support [Riehle et al. DOI:10.3389/fcvm.2022.881067]. Its expression levels were positively correlated with cardiac output, identifying it as a potential prognostic biomarker for organ hypoperfusion and ischemia in this acute condition.