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Reflecting on the clinical implications, St-Pierre says that the findings support cautious use of GLP-1 RAs in selected patients with IBD when prescribed for approved metabolic indications, with appropriate counselling and monitoring. At the same time, she noted that the findings highlight substantial evidence gaps and believes future research should move beyond proxy outcomes and incorporate prospective, IBD-specific designs that integrate objective inflammatory measures with robust metabolic phenotyping. Moreover, there should be special considerations on the effects of GLP-1 RAs on body composition of patients with IBD, she adds
That combination carries a real hypoglycaemia risk needing planning with your diabetes team
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None of these outcomes are acceptable when you are injecting something into your body
Pharmacokinetic (PK) profiling in both species revealed linear doseexposure relationships, with [H] BPC157 rapidly metabolized into small peptides and ultimately tritium-labeled proline for normal amino acid catabolism/excretion [11]
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