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In this article, we review the latest research to highlight when these medications might offer the greatest benefit for patients with substance use disorders.

In the subgroup analyses, human GLP-1 RAs, but not nonhuman GLP-1 RAs, reduced the risk of MACE in patients with HF (p interaction = 0.11)

GLP-1 and GIP levels rose in the first postoperative year and diminished thereafter

The GLP-1-induced enhancement of evoked EPSCs was abolished by a selective GLP-1 receptor antagonist, exendin 939, as well as by the extracellular application of a specific protein kinase A (PKA) inhibitor, KT5720