Answers are grounded in this paper and cite their sources.
In Brief Objective: To evaluate the association between glucagon-like peptide 1 (GLP-1) secretion and the long-term (>2 years) outcome of type 2 diabetes mellitus (T2DM) after Roux-en-Y gastric bypass (RYGBP). Methods: Cross-sectional study in 18 T2DM morbidly obese subjects who underwent RYGBP but differed in the long-term outcome of T2DM (remission: G1, n = 6; relapse: G2, n = 6; lack of remission: G3: n = 6). Groups were matched for their sex, age, and body mass index. The GLP-1, glucose, C-peptide, and glucagon responses to a standardized test meal (STM) were evaluated. Insulin secretion and insulin sensitivity were estimated from the STM and by frequently sampling intravenous glucose tolerance test (FSIVGTT). Dual-energy X-ray absorptiometry was used to assess body composition. Results: Patients in G1 presented a lower area under the curve (AUC0–120) of glucose in response to the STM as compared with G2, and G3 (P < 0.01). In contrast, the AUC0–120 of GLP-1 (P = 0.884) and glucagon (P = 0.630) did not differ significantly among the 3 groups. Indices of insulin secretion adjusted by the prevailing insulin sensitivity derived from STM and FSIVGTT, demonstrated larger β-cell function in subjects in G1 as compared with G2 or G3 (Disposition Index-STM, P = 0.005; DI-FSIVGTT, P = 0.006). Body composition and inflammatory markers did not differ significantly among the 3 study groups. Conclusions: Our data show that in subjects with T2DM an enhanced GLP-1 response to meal intake is not sufficient to maintain normal glucose tolerance in the long term after RYGBP. Our data suggest that β-cell function is a key determinant of the long-term remission of T2DM after this bariatric surgery technique. In patients with type 2 diabetes mellitus (T2DM) before surgery, Roux-en-Y gastric bypass (RYGBP) is associated with an enhanced glucagon-like peptide 1 (GLP-1) response to meal intake in the long term after surgery. However, the enlarged GLP-1 response is not necessarily associated with remission of the T2DM. In contrast, our data suggest that β-cell function is an important factor in determining long-term remission of T2DM after RYGBP.
No takes yet. Share an insight, caveat, or question.
Jiménez et al. (2012) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: