Recovery Of The Incretin Effect In Type 2 Diabetic Patients After Biliopancreatic Diversion.


Autoria(s): Novaes, Fernanda S; Vasques, Ana C J; Pareja, José C; Knop, Filip K; Tura, Andrea; Chaim, Élinton A; Geloneze, Bruno
Contribuinte(s)

UNIVERSIDADE DE ESTADUAL DE CAMPINAS

Data(s)

01/03/2015

27/11/2015

27/11/2015

Resumo

Context: Bariatric surgery often results in remission of the diabetic state in obese patients. Increased incretin effect seems to play an important role in the glycemic improvements after Roux-en-Y gastric bypass, but the impact of biliopancreatic diversion (BPD) remains unexplored. Objective: To elucidate the effect of BPD on the incretin effect and its interplay with beta-cell function and insulin sensitivity (IS) in obese subjects with type 2 diabetes (T2DM). Design, Setting and Patients: Twenty-three women were studied: a control group of 13 lean, normal glucose-tolerant women (lean NGT) studied once and 10 obese patients with T2DM studied before, 1 and 12 months after BPD. Intervention: The ObeseT2DM group underwent BPD. Main Outcome Measures: The change in incretin effect as measured by the isoglycemic intravenous glucose infusion test. Secondary outcomes encompassed IS and beta-cell function. Results: At baseline, the incretin effect was lower in obese T2DM compared to lean NGT (p<0.05). One month after BPD, the incretin effect was not changed, but at 12 months it reached the level of the lean NGT group (p>0.05). IS improved (p<0.05) 1 month after BPD and at 12 months it resembled the levels of the lean NGT group. Insulin secretory rate and beta-cell glucose sensitivity increased after BPD and achieved levels similar to lean NGT group 1 month after BPD and even higher levels at 12 months (p<0.05). Conclusions: BPD has no acute impact on the reduced incretin effect, but 12 months after surgery the incretin effect normalizes alongside normalization of glucose control, IS and beta-cell function.

jc20144042

Identificador

The Journal Of Clinical Endocrinology And Metabolism. , p. jc20144042, 2015-Mar.

1945-7197

10.1210/jc.2014-4042

http://www.ncbi.nlm.nih.gov/pubmed/25742514

http://repositorio.unicamp.br/jspui/handle/REPOSIP/202185

25742514

Idioma(s)

eng

Relação

The Journal Of Clinical Endocrinology And Metabolism

J. Clin. Endocrinol. Metab.

Direitos

fechado

Fonte

PubMed

Tipo

Artigo de periódico