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These results indicate that the increased amount of non-12-OH FXR-antagonistic BAs consequent to the decrease in CYP8B1 expression after T3 treatment potentiates GLP-1 production by deactivating the intestinal FXR, thereby improving glucose homeostasis via the augmentation of insulin secretion
Program rules could prove challenging To get medications covered under the new program, providers must submit a prior authorization request and a prescription for an eligible GLP-1 drug for an approved use
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Their relative simplicity of use and administration is attracting a greater number of patients requiring minimal intervention and broadening the current treatment market
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