Cersosimo Eugenio, Solis-Herrera Carolina, Trautmann Michael E, Malloy Jaret, Triplitt Curtis L
Texas Diabetes Institute, University of Texas Health Science Center-San Antonio, 701 S. Zarzamora, MS 10-5, San Antonio, TX 78207, USA.
Curr Diabetes Rev. 2014 Jan;10(1):2-42. doi: 10.2174/1573399810666140214093600.
Type 2 diabetes mellitus (T2DM) is characterized by a progressive failure of pancreatic β-cell function (BCF) with insulin resistance. Once insulin over-secretion can no longer compensate for the degree of insulin resistance, hyperglycemia becomes clinically significant and deterioration of residual β-cell reserve accelerates. This pathophysiology has important therapeutic implications. Ideally, therapy should address the underlying pathology and should be started early along the spectrum of decreasing glucose tolerance in order to prevent or slow β-cell failure and reverse insulin resistance. The development of an optimal treatment strategy for each patient requires accurate diagnostic tools for evaluating the underlying state of glucose tolerance. This review focuses on the most widely used methods for measuring BCF within the context of insulin resistance and includes examples of their use in prediabetes and T2DM, with an emphasis on the most recent therapeutic options (dipeptidyl peptidase-4 inhibitors and glucagon-like peptide-1 receptor agonists). Methods of BCF measurement include the homeostasis model assessment (HOMA); oral glucose tolerance tests, intravenous glucose tolerance tests (IVGTT), and meal tolerance tests; and the hyperglycemic clamp procedure. To provide a meaningful evaluation of BCF, it is necessary to interpret all observations within the context of insulin resistance. Therefore, this review also discusses methods utilized to quantitate insulin-dependent glucose metabolism, such as the IVGTT and the euglycemic-hyperinsulinemic clamp procedures. In addition, an example is presented of a mathematical modeling approach that can use data from BCF measurements to develop a better understanding of BCF behavior and the overall status of glucose tolerance.
2型糖尿病(T2DM)的特征是胰腺β细胞功能(BCF)逐渐衰竭并伴有胰岛素抵抗。一旦胰岛素过度分泌无法再补偿胰岛素抵抗的程度,高血糖就会在临床上变得显著,残余β细胞储备的恶化也会加速。这种病理生理学具有重要的治疗意义。理想情况下,治疗应针对潜在的病理状况,并且应在葡萄糖耐量逐渐降低的整个过程中尽早开始,以预防或减缓β细胞衰竭并逆转胰岛素抵抗。为每位患者制定最佳治疗策略需要准确的诊断工具来评估葡萄糖耐量的潜在状态。本综述重点关注在胰岛素抵抗背景下测量BCF最广泛使用的方法,并包括其在糖尿病前期和T2DM中使用的示例,重点是最新的治疗选择(二肽基肽酶-4抑制剂和胰高血糖素样肽-1受体激动剂)。BCF测量方法包括稳态模型评估(HOMA);口服葡萄糖耐量试验、静脉葡萄糖耐量试验(IVGTT)和进餐耐量试验;以及高血糖钳夹程序。为了对BCF进行有意义的评估,有必要在胰岛素抵抗的背景下解释所有观察结果。因此,本综述还讨论了用于定量胰岛素依赖性葡萄糖代谢的方法,如IVGTT和正常血糖-高胰岛素钳夹程序。此外,还给出了一个数学建模方法的示例,该方法可以使用BCF测量数据来更好地理解BCF行为和葡萄糖耐量的整体状态。