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Existing GLP-1 therapies function as drugs that make patients eat less, while retatrutide, by also targeting the glucagon receptor, adds a function that enables the body to burn more fat
Animal model studies have suggested that GLP-1RAs may cause pancreatitis and exocrine dysplasia, but in the large RCTs and a meta-analysis, GLP-1RAs did not increase the risk of pancreatitis or pancreatic cancer [82,83]
drafted a systematic review of over 300 papers on the impact of GLP1s and pancreatitis
When compared to dulaglutide and placebo, tirzepatide statistically significantly displayed improvement in ALT and AST from baseline
Moro blood orange does have preliminary evidence for supporting fat metabolism
Importantly, it does not typically drive insulin release under low-glucose conditions, reducing hypoglycemia risk in research settings
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