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Moreover, AGE-D modified the systemic glycosylation profile, as examined by lectin microarray, and increased Nε-carboxymethyllysine immunoreactivity and AGEs receptor amounts in ileum and submandibular glands. These results were associated to increased systemic degrees of cytokines and impaired gut microbial composition and homeostasis. Significant correlations were recorded between changes in microbial population plus in incretins and inflammatory markers amounts. Overall, our data shows
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