Department of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Endocr Pract. 2010 Nov-Dec;16(6):1038-55. doi: 10.4158/EP10112.RA.
To review available data on preservation and potential improvement of beta-cell function in patients with type 2 diabetes mellitus (T2DM) with use of currently available strategies and agents.
Using key words, we performed a MEDLINE search of the relevant literature published through 2009 regarding the effects of available agents on beta-cell function in humans with T2DM.
On the basis of current clinical data, no uniformly effective treatment for beta-cell preservation has been found. Lifestyle intervention and early intensive insulin therapy appear to have some preservative properties on beta-cell function. Glucagonlike peptide-1 agonists, dipeptidyl- peptidase-4 inhibitors, and thiazolidinediones result in maintenance and often improvement of beta-cell function during their active use; however, data on their ability to preserve beta-cell function when patients are not receiving active treatment are limited.
The continuous loss of beta-cell mass and beta-cell function is a critical mechanism underlying the progressive deterioration of glycemic control in T2DM. In light of the projected increase in individuals at risk for developing T2DM, strategies and agents aimed at delaying or preventing the progression and inducing a remission of the disease are needed. Future research on this topic should include comparative efficacy trials with washout periods incorporating currently available and novel medications and strategies for preservation of beta cells.
回顾目前可用于 2 型糖尿病(T2DM)患者β细胞功能保存和潜在改善的策略和药物,评估相关数据。
使用关键词,检索了 2009 年以前发表的有关 T2DM 患者现有药物对β细胞功能影响的 MEDLINE 相关文献。
基于目前的临床数据,尚未发现一种对β细胞保存具有普遍有效作用的治疗方法。生活方式干预和早期强化胰岛素治疗似乎对β细胞功能具有一定的保护作用。胰高血糖素样肽-1 激动剂、二肽基肽酶-4 抑制剂和噻唑烷二酮类药物在使用过程中能维持β细胞功能,且常常能改善β细胞功能;但关于在未接受积极治疗时这些药物能否保存β细胞功能的数据有限。
β细胞数量和功能的持续丧失是导致 T2DM 患者血糖控制逐渐恶化的关键机制。鉴于未来发生 T2DM 风险增加的个体数量,需要寻找并应用新的策略和药物来延迟或预防疾病的进展,并诱导疾病缓解。关于这一主题的未来研究应包括包含现有和新型药物的洗脱期比较疗效试验,以及β细胞保存的策略。