Duodenal neuroendocrine cells and neuromedin U in subjects with obesity: Relationship with type 2 diabetes and glucose homeostasis.

Duodenal endocrine cells contribute to the incretin response, yet their changes in obesity and type 2 diabetes (T2D) remain controversial. We quantified expression of chromogranin A, glucagon-like peptide-1 (GLP-1), serotonin, and neuromedin U (NmU) in duodenal biopsies from 34 participants with obesity (19 with T2D, 15 without) and six healthy controls. Compared to controls, the patients with obesity showed significantly higher proportions of chromogranin A (p = 0.007), GLP-1 (p = 0.006), and serotonin (p = 0.013) expressing cells, irrespective of T2D status. GLP-1 expression correlated with HbA1C (r = 0.454, p = 0.005) and meal test glucose (r = 0.455, p = 0.0018) but not with insulin. Chromogranin A expression correlated with both GLP-1 (r = 0.486, p = 0.003) and serotonin (r = 0.475, p = 0.003), as well as BMI (r = 0.429, p = 0.007). NmU was detected in the lamina propria but did not differ among groups. For NmU, an association with insulin (incremental AUC, r = 0.363, p = 0.045) was observed. In conclusion, obesity was associated with hyperplasia of duodenal GLP-1, serotonin, and chromogranin A cells. The link between GLP-1 expression, HbA1C, and meal test glucose indicates that, despite increased numbers of GLP-1-producing cells, individuals with obesity may still experience insufficient incretin action. No evidence supported a role for NmU as a human decretin in these patients.