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Jejunal Gipr mRNA levels were unchanged in cold-stressed male and female WT mice, and not detected in DIRKO mice (Fig

1,2 t Time-to-first-event outcomes were analyzed with a stratified Cox proportional-hazards model with treatment as a fixed factor and stratified according to SGLT-2 inhibitor use at baseline

J Phys Chem B

Exclusion criteria included less than 3 months of semaglutide use, history of bariatric surgery, and active malignancy

Results of the statistical analysis of semaglutide pharmacokinetic endpoints are presented in Table 1

Potential risks identified in animal studies: Animal studies have shown that Semaglutide can cause adverse effects such as fetal malformations, pregnancy loss, and growth retardation