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This stratified approach avoids the one-size-fits-all assumptions that have constrained past indication extension attempts and provides a clearer, evidence-led path to expanding GLP-1 use where it is biologically and clinically justified.

Experiments on mouse chondrocytes also revealed the added role of liraglutide in reducing inflammation by decreasing mRNA expression of inducible nitric oxide synthase, matrix metallopeptidase 13, and ADAM metallopeptidase with thrombospondin type 1 motif 5, culminating in a reduction of IL-6, prostaglandin E2, and nitric oxide[13]

These cells, derived from subcutaneous abdominal adipose tissue, preserved their adipogenic capacity and can differentiate into mature adipocytes [24]

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