A study in human brain tissue demonstrated that hsa-miR-21-5p is upregulated in traumatic brain injury (TBI) cases compared to non-traumatic controls and its expression is significantly higher in cases with short survival (<1 day) and in the critical–fatal TBI severity subgroup, while being lower in cases with long survival (>7 days) [Consalvo et al. DOI:10.3390/ijms25179539]. In human skin, the mir-21 is upregulated in burn hypertrophic scar tissue and its derived fibroblasts compared to normal controls, where it promotes keratinocyte proliferation and migration, stimulates re-epithelialisation, and is associated with scarring [Siu et al. DOI:10.1111/wrr.13100]. A study in humans demonstrated that serum levels of the mir-21 were significantly higher, up to 10-fold, in patients with erectile dysfunction (ED) alone compared to those with cardiovascular disease (CVD) alone or the combination of CVD and ED [Agulló et al. DOI:10.3389/fcvm.2024.1301925].