Details

Autor(en) / Beteiligte

• Mannucci, E.
• Pala, L.
• Monami, M.
• Vico, L.
• Bardini, G.
• Dicembrini, I.
• Ciani, S.
• Lamanna, C.
• Marchionni, N.
• Rotella, C. M.

Titel

Glucagon-like peptide-1 response to meals and post-prandial hyperglycemia in Type 2 diabetic patients

Ist Teil von

• Journal of endocrinological investigation, 2010-03, Vol.33 (3), p.147-150

Ort / Verlag

Cham: Springer International Publishing

Erscheinungsjahr

2010

Quelle

MEDLINE

Beschreibungen/Notizen

• Background : The impaired response of glucagon-like peptide-1 (GLP-1) to meals in diabetic patients can contribute to the pathogenesis of impaired insulin secretion and post-prandial hyperglycemia. This study is aimed at the assessment of the relationship between meal-induced GLP-1 and post-prandial hyperglycemia in Type 2 diabetic patients. Methods : Twenty-one drug-naïve Type 2 diabetic patients were studied. Blood glucose and active GLP-1 levels were measured 0, 30, 60, 90, and 120 min after a standard test meal. A continuous glucose monitoring (CGM) system was applied for the following 3 days. Nutrient intake at each meal was calculated on the basis of patients’ food records. For each patient, post-prandial 120-min glucose incremental area under the curve (iAUC) was included in linear regression model exploring its relationship with total energy and carbohydrate intake, and the angular coefficient for total energy (EAC) and carbohydrate (CAC) was calculated. Results : GLP-1 levels peaked 30 min after the test meal. Logarithmically transformed 60-min GLP-1 iAUC showed a significant inverse correlation with glycated hemoglobin (HbA 1c ) ( p <0.01). A significant inverse correlation of 60-min GLP-1 iAUC was also observed with EAC and CAC (both p <0.01), meaning that patients with a lower GLP-1 response to the test meal had a higher increment of post-prandial glucose for each additional unit of total energy or carbohydrate intake. Conclusions : In Type 2 diabetic patients, a lower GLP-1 response to meals is associated with a higher HbA 1c , and with a greater degree of meal-induced hyperglycemia, both in a meal test and during CGM in “real-life” conditions.