Mechanisms of Diabetes Improvement Following Bariatric/Metabolic Surgery

被引:289
作者
Batterham, Rachel L. [1 ,2 ,3 ]
Cummings, David E. [4 ,5 ]
机构
[1] UCL, Dept Med, Obes Res Ctr, London, England
[2] Univ Coll London Hosp, Bariatr Ctr Weight Management & Metab Surg, London, England
[3] Univ Coll London Hosp, Natl Inst Hlth Res, Biomed Res Ctr, London, England
[4] Univ Washington, VA Puget Sound Hlth Care Syst, Seattle, WA 98195 USA
[5] Univ Washington, Diabet & Obes Ctr Excellence, Seattle, WA 98195 USA
关键词
Y GASTRIC BYPASS; VERTICAL SLEEVE GASTRECTOMY; BETA-CELL FUNCTION; DUODENAL-JEJUNAL BYPASS; BARIATRIC SURGERY; WEIGHT-LOSS; BILE-ACIDS; INSULIN SENSITIVITY; HYPERINSULINEMIC HYPOGLYCEMIA; GLUCOSE EFFECTIVENESS;
D O I
10.2337/dc16-0145
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
More than 20 years ago, Pories et al. published a seminal article, Who Would Have Thought It? An Operation Proves to Be the Most Effective Therapy for Adult-Onset Diabetes Mellitus. This was based on their observation that bariatric surgery rapidly normalized blood glucose levels in obese people with type 2 diabetes mellitus (T2DM), and 10 years later, almost 90% remained diabetes free. Pories et al. suggested that caloric restriction played a key role and that the relative contributions of proximal intestinal nutrient exclusion, rapid distal gut nutrient delivery, and the role of gut hormones required further investigation. These findings of T2DM improvement/remission after bariatric surgery have been widely replicated, together with the observation that bariatric surgery prevents or delays incident T2DM. Over the ensuing two decades, important glucoregulatory roles of the gastrointestinal (GI) tract have been firmly established. However, the physiological and molecular mechanisms underlying the beneficial glycemic effects of bariatric surgery remain incompletely understood. In addition to the mechanisms proposed by Pories et al., changes in bile acid metabolism, GI tract nutrient sensing and glucose utilization, incretins, possible anti-incretin(s), and the intestinal microbiome are implicated. These changes, acting through peripheral and/or central pathways, lead to reduced hepatic glucose production, increased tissue glucose uptake, improved insulin sensitivity, and enhanced -cell function. A constellation of factors, rather than a single overarching mechanism, likely mediate postoperative glycemic improvement, with the contributing factors varying according to the surgical procedure. Thus, different bariatric/metabolic procedures provide us with experimental tools to probe GI tract physiology. Embracing this approach through the application of detailed phenotyping, genomics, metabolomics, and gut microbiome studies will enhance our understanding of metabolic regulation and help identify novel therapeutic targets.
引用
收藏
页码:893 / 901
页数:9
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