饮食或减肥手术所致体重减轻后葡萄糖依赖性胰岛素性多肽和胰高血糖素的变化。

Amanda Finn, Yenni Cedillo, Marthe Aukan, Barbara Gower, Catia Martins
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引用次数: 0

摘要

目的:本研究比较了极低能量饮食(VLED)单独或联合袖式胃切除术(SG)或Roux-en-Y胃旁路术(RYGB)对葡萄糖依赖性胰岛素性多肽(GIP)和胰高血糖素浓度的影响,这些激素可能在维持体重中发挥作用。方法:重度肥胖患者接受10周VLED单独治疗(n = 15)或联合SG治疗(n = 15)或RYGB治疗(n = 14)。在干预前和干预后测量血浆胰高血糖素和GIP浓度(空腹和餐后60分钟)、胰岛素敏感性、呼吸商和静息能量消耗(REE)。评估随访时各组间激素浓度的差异以及激素与代谢结果之间的关系。结果:与SG相比,RYGB后空腹胰高血糖素浓度较高,而餐后GIP浓度较低。RYGB组餐后胰高血糖素升高与松田指数下降有关,与各组REE升高有关。空腹GIP的增加与HOMA-IR的增加相关。结论:与其他组相比,RYGB与较低的餐后GIP和较高的胰高血糖素浓度相关。这些激素的变化可能会影响REE,以及胰岛素敏感性,潜在地调节减肥维持的可能性。试验注册:ClinicalTrials.gov标识符NCT04051190。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glucose-Dependent Insulinotropic Polypeptide and Glucagon After Weight Loss Induced by Diet or Bariatric Surgery.

Objective: This study compared the effects of a very low-energy diet (VLED), alone or combined with sleeve gastrectomy (SG) or Roux-en-Y gastric bypass (RYGB), on glucose-dependent insulinotropic polypeptide (GIP) and glucagon concentrations, hormones likely to play a role in weight loss maintenance.

Methods: Participants with severe obesity underwent 10 weeks of VLED alone (n = 15) or combined with SG (n = 15) or RYGB (n = 14). Plasma concentrations of glucagon and GIP (fasting and the first 60 min of a meal), insulin sensitivity, respiratory quotient, and resting energy expenditure (REE) were measured at pre- and post-intervention. Differences in hormone concentrations between groups at follow-up and associations between hormones and metabolic outcomes were evaluated.

Results: Fasting glucagon concentrations were higher, while postprandial GIP concentrations were lower, after RYGB compared to SG. An increase in postprandial glucagon was associated with a decrease in Matsuda index in the RYGB group and with an increase in REE in all groups. An increase in fasting GIP was correlated with an increase in HOMA-IR.

Conclusions: RYGB was associated with lower postprandial GIP and greater glucagon concentrations compared with other groups. These hormonal changes are likely to impact REE, as well as insulin sensitivity, potentially modulating the likelihood of weight loss maintenance.

Trial registration: ClinicalTrials.gov identifier NCT04051190.

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