Clinical Medicine, Feinberg School of Medicine, 676 N Saint Clair, Ste 415, Chicago, IL 60611, USA.
Mayo Clin Proc. 2010 Dec;85(12 Suppl):S50-9. doi: 10.4065/mcp.2010.0471. Epub 2010 Nov 24.
Traditionally, successful treatment of patients with type 2 diabetes mellitus (DM) has been defined strictly by achievement of targeted glycemic control, primarily using a stepped-care approach that begins with changes in lifestyle combined with oral therapy that is slowly intensified as disease progression advances and β-cell function declines. However, stepped care is often adjusted without regard to the mechanism of hyperglycemia or without long-term objectives. A more comprehensive definition of treatment success in patients with type 2 DM should include slowing or stopping disease progression and optimizing the reduction of all risk factors associated with microvascular and macrovascular disease complications. To achieve these broader goals, it is important to diagnose diabetes earlier in the disease course and to consider use of more aggressive combination therapy much earlier with agents that have the potential to slow or halt the progressive β-cell dysfunction and loss characteristic of type 2 DM. A new paradigm for managing patients with type 2 DM should address the concomitant risk factors and morbidities of obesity, hypertension, and dyslipidemia with equal or occasionally even greater aggressiveness than for hyperglycemia. The use of antidiabetes agents that may favorably address cardiovascular risk factors should be considered more strongly in treatment algorithms, although no pharmacological therapy is likely to be ultimately successful without concomitant synergistic lifestyle changes. Newer incretin-based therapies, such as glucagon-like peptide 1 receptor agonists and dipeptidyl peptidase 4 inhibitors, which appear to have a favorable cardiovascular safety profile as well as the mechanistic possibility for a favorable cardiovascular risk impact, are suitable for earlier inclusion as part of combination regimens aimed at achieving comprehensive treatment success in patients with type 2 DM.
传统上,2 型糖尿病(DM)患者的成功治疗严格定义为实现目标血糖控制,主要采用逐步治疗方法,首先改变生活方式,结合口服治疗,随着疾病进展和β细胞功能下降逐渐加强。然而,逐步治疗通常是在不考虑高血糖机制或没有长期目标的情况下进行调整的。2 型糖尿病患者治疗成功的更全面定义应包括减缓或停止疾病进展并优化所有与微血管和大血管疾病并发症相关的风险因素的降低。为了实现这些更广泛的目标,重要的是在疾病过程中更早地诊断糖尿病,并考虑更早地使用更具侵略性的联合疗法,这些疗法具有减缓或阻止 2 型糖尿病特征性β细胞功能进行性丧失的潜力。管理 2 型糖尿病患者的新范例应同等或甚至更积极地解决肥胖、高血压和血脂异常的伴随风险因素和合并症,而不仅仅是针对高血糖。尽管没有协同的生活方式改变,任何药物治疗都不太可能最终成功,但应更强烈地考虑使用可能有利于心血管风险因素的抗糖尿病药物作为治疗算法的一部分。新型基于肠促胰岛素的疗法,如胰高血糖素样肽 1 受体激动剂和二肽基肽酶 4 抑制剂,似乎具有良好的心血管安全性,并且具有有利于心血管风险的机制可能性,适合更早地纳入旨在实现 2 型糖尿病患者全面治疗成功的联合治疗方案。