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Not all adolescents respond equally to GLP-1 therapies, suggesting that genetic and metabolic profiling could help determine which patients benefit most from single, dual (GLP-1/GIP or GLP-1/GCGR), or triple agonists

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( d ) Representative immunohistochemistry for HCAR2 in early intestinal adenomas from CD- and KD-fed mice

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and 4.5%, thiazolidinediones), we found that in the matched cohort (eTable 5), GLP-1RA was associated with a lower risk of AF, ischemic stroke, and cardiovascular mortality (eTable 6 and eFigure 4 & 5)

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