Frezza Ermenegildo Eldo
Division of Minimal Invasive and Bariatric Surgery, Department of Surgery, Texas Tech University Health Science Center, Lubbock, TX 79145, USA.
Obes Surg. 2004 Aug;14(7):999-1005. doi: 10.1381/0960892041719699.
Morbid obesity is a serious health problem associated with disease and mortality. One such disease is non-insulin-dependent diabetes mellitus (NIDDM). Approximately 95% of American diabetics have NIDDM. One of the major causes for type 2 diabetes is obesity. The improvement of diabetes with weight control is not in the earliest description of the disease. However, dietary control of NIDDM is often disappointing. Diet can improve glucose metabolism in obesity, but the improvement usually represents only a portion or a brief return to euglycemia, even when patients appear to be compliant. In contrast, reversal of NIDDM has been much more successfully achieved after bariatric surgery. Intra-abdominal fat deposition is associated with increased plasma concentration of free fatty acids, which reduce insulin sensitivity at both muscular and hepatic sites. The progression of diabetes is heralded by the inability of the beta-cells to maintain their previously high rate of insulin secretion in response to glucose, in the face of insulin resistance. The propensity to develop type 2 diabetes may be genetically determined or triggered by environmental factors. The connection between diabetes and obesity represents a continuum that progresses through different phases in which defective insulin action is the principal problem. At this point, we are unable to correlate the different findings of the many questions that arise, such as: 1) Does the decrease in sensitivity to insulin result from rearrangement of the insulin receptor? 2) Is weight loss the trigger for decrease of insulin resistance? 3) Is rearrangement of part of the intestine a mechanism to trigger the secretion of hormones (incretins) that help in insulin response? 4) Which mechanism controls the insulin resistance? The goal of this paper is to review literature on incretins and address the role of incretins after bariatric surgery. We know very little about the action of incretins in diabetes. We will assess the interaction between the secretion of incretins and bariatric surgery for the cure of diabetes.
病态肥胖是一个与疾病和死亡率相关的严重健康问题。非胰岛素依赖型糖尿病(NIDDM)就是其中一种疾病。大约95%的美国糖尿病患者患有NIDDM。2型糖尿病的主要病因之一是肥胖。通过控制体重改善糖尿病并非该病最早的描述内容。然而,NIDDM的饮食控制往往令人失望。饮食可改善肥胖患者的葡萄糖代谢,但即便患者看似依从,这种改善通常也只是部分改善或短暂恢复至血糖正常状态。相比之下,减肥手术后NIDDM的逆转更为成功。腹部脂肪沉积与游离脂肪酸血浆浓度升高有关,这会降低肌肉和肝脏部位的胰岛素敏感性。面对胰岛素抵抗,β细胞无法维持其先前对葡萄糖的高胰岛素分泌率预示着糖尿病的进展。患2型糖尿病的倾向可能由基因决定或由环境因素触发。糖尿病与肥胖之间的联系代表了一个连续过程,该过程会经历不同阶段,其中胰岛素作用缺陷是主要问题。目前,我们无法将出现的诸多问题的不同研究结果联系起来,例如:1)对胰岛素敏感性的降低是否源于胰岛素受体的重排?2)体重减轻是否是胰岛素抵抗降低的触发因素?3)肠道部分重排是否是触发有助于胰岛素反应的激素(肠促胰岛素)分泌的一种机制?4)哪种机制控制胰岛素抵抗?本文的目的是回顾有关肠促胰岛素的文献,并探讨减肥手术后肠促胰岛素的作用。我们对肠促胰岛素在糖尿病中的作用了解甚少。我们将评估肠促胰岛素分泌与减肥手术在治疗糖尿病方面的相互作用。