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However, the mechanistic role of this modulation in microbial communities has not been reported and has to be further elucidated with in vitro or in vivo experiments [208]

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Our studies also eliminate the possibility that enterocyte-derived DPP-4, accounting for about 90% of gut DPP-4, is the pool responsible for glucose- and lipid-lowering effects of either gut-selective or systemic doses of DPP4i

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Sulfonylureas were prescribed to 17.2% of adults