The Metabolomic Effects of Tripeptide Gut Hormone Infusion Compared to Roux-en-Y Gastric Bypass and Caloric Restriction

医学 肽YY 内科学 背景(考古学) Roux-en-Y吻合术 胰高血糖素样肽-1 代谢组学 利拉鲁肽 减肥 激素 葡萄糖稳态 内分泌学 胰岛素 2型糖尿病 糖尿病 胃分流术 肥胖 生物信息学 胰岛素抵抗 生物 古生物学 受体 神经肽Y受体 神经肽
作者
Ben Jones,Caroline Sands,Κλεοπάτρα Αλεξιάδου,James Minnion,George Tharakan,Preeshila Behary,Ahmed R. Ahmed,Sanjay Purkayastha,Matthew R. Lewis,Stephen R. Bloom,Jia V. Li,Tricia Tan
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [Oxford University Press]
卷期号:107 (2): e767-e782 被引量:22
标识
DOI:10.1210/clinem/dgab608
摘要

Abstract Context The gut-derived peptide hormones glucagon-like peptide-1 (GLP-1), oxyntomodulin (OXM), and peptide YY (PYY) are regulators of energy intake and glucose homeostasis and are thought to contribute to the glucose-lowering effects of bariatric surgery. Objective To establish the metabolomic effects of a combined infusion of GLP-1, OXM, and PYY (tripeptide GOP) in comparison to a placebo infusion, Roux-en-Y gastric bypass (RYGB) surgery, and a very low-calorie diet (VLCD). Design and Setting Subanalysis of a single-blind, randomized, placebo-controlled study of GOP infusion (ClinicalTrials.gov NCT01945840), including VLCD and RYGB comparator groups. Patients and Interventions Twenty-five obese patients with type 2 diabetes or prediabetes were randomly allocated to receive a 4-week subcutaneous infusion of GOP (n = 14) or 0.9% saline control (n = 11). An additional 22 patients followed a VLCD, and 21 underwent RYGB surgery. Main Outcome Measures Plasma and urine samples collected at baseline and 4 weeks into each intervention were subjected to cross-platform metabolomic analysis, followed by unsupervised and supervised modeling approaches to identify similarities and differences between the effects of each intervention. Results Aside from glucose, very few metabolites were affected by GOP, contrasting with major metabolomic changes seen with VLCD and RYGB. Conclusions Treatment with GOP provides a powerful glucose-lowering effect but does not replicate the broader metabolomic changes seen with VLCD and RYGB. The contribution of these metabolomic changes to the clinical benefits of RYGB remains to be elucidated.

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