Rosenstock J
Dallas Diabetes and Endocrine Center, Medical City, Dallas, TX 75230, USA.
Diabetes Obes Metab. 2007 Sep;9 Suppl 1:3-11. doi: 10.1111/j.1463-1326.2007.00768.x.
Given the enormous public health and economic burden posed by the global epidemic of type 2 diabetes mellitus (T2DM), intervention in the prediabetes stage of disease to prevent progression to T2DM and its vascular complications seems the most sensible approach. Precisely how best to intervene remains the subject of much debate. Prudent lifestyle changes have been shown to significantly reduce the risk of progression in individuals with impaired fasting glucose (IFG) and impaired glucose tolerance (IGT). Although lifestyle modifications are notoriously difficult to maintain, there is evidence that intensive intervention results in continued preventive benefit after the stopping of structured counselling. A number of drug therapies, including metformin, acarbose, orlistat and rosiglitazone, have also been proven effective in preventing progression from IFG/IGT, but unresolved issues still remain. Specifically, whether large numbers of individuals with glucose dysregulation who may never progress to T2DM should be exposed to the risk of pharmacological adverse effects is a topic of discussion and debate. Furthermore, there are limited data on the effectiveness of implementing interventions during the prediabetic state to prevent cardiovascular complications that may be hyperglycaemia related. A recent American Diabetes Association (ADA) consensus statement on IFG/IGT recommends lifestyle modification for individuals with IFG or IGT. Of note, the ADA consensus statement introduces the option of adding metformin treatment to lifestyle changes in those individuals who have combined IFG/IGT plus an additional risk factor for progression and who also have some features that increase the likelihood of benefiting from metformin treatment. The dipeptidyl peptidase-4 inhibitors are a new class of oral antidiabetic agents that, in addition to being effective in improving glycaemic control, may exert beneficial effects in preserving beta-cell function. These characteristics, combined with a low risk of hypoglycaemia, weight neutrality and what appears - so far - to be a relatively benign tolerability profile, make these agents intriguing candidates for preventive treatment.
鉴于2型糖尿病(T2DM)全球流行所带来的巨大公共卫生和经济负担,在疾病的糖尿病前期阶段进行干预以预防进展为T2DM及其血管并发症似乎是最明智的方法。究竟如何进行最佳干预仍是众多争论的主题。已表明谨慎的生活方式改变可显著降低空腹血糖受损(IFG)和糖耐量受损(IGT)个体的疾病进展风险。尽管众所周知生活方式改变难以维持,但有证据表明强化干预在停止结构化咨询后仍能持续带来预防益处。多种药物疗法,包括二甲双胍、阿卡波糖、奥利司他和罗格列酮,也已被证明在预防IFG/IGT进展方面有效,但仍存在未解决的问题。具体而言,大量可能永远不会进展为T2DM的血糖失调个体是否应暴露于药物不良反应风险中是一个讨论和争论的话题。此外,关于在糖尿病前期状态实施干预以预防可能与高血糖相关的心血管并发症的有效性的数据有限。美国糖尿病协会(ADA)最近关于IFG/IGT的共识声明建议IFG或IGT个体进行生活方式改变。值得注意的是,ADA共识声明引入了在那些合并IFG/IGT且有进展的额外风险因素、同时具有一些增加从二甲双胍治疗中获益可能性特征的个体中,在生活方式改变基础上加用二甲双胍治疗的选择。二肽基肽酶-4抑制剂是一类新型口服抗糖尿病药物,除了有效改善血糖控制外,可能在保护β细胞功能方面发挥有益作用。这些特性,再加上低血糖风险低、体重中性以及目前看来相对良好的耐受性,使这些药物成为预防性治疗的有趣候选药物。