Time for Testing Incretin Therapies in Early Type 1 Diabetes?

被引:24
作者
Bosi, Emanuele [1 ,2 ,3 ]
机构
[1] Ist Sci San Raffaele, Dept Internal Med, I-20132 Milan, Italy
[2] Ist Sci San Raffaele, Diabet Res Inst, I-20132 Milan, Italy
[3] Univ Vita Salute San Raffaele, I-20132 Milan, Italy
关键词
BETA-CELL FUNCTION; MICE; INHIBITION; TRIAL;
D O I
10.1210/jc.2009-2741
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Incretin-based compounds, including glucagon-like peptide-1 receptor agonists and dipeptidylpeptidase4 inhibitors, have emerged as a new class of agents for the treatment of type 2 diabetes. In this article, the potential and supporting evidence for extending their use to early type 1 diabetes are reviewed. The rationale relies on the assumption that these drugs, in addition to their action on insulin secretion and glucose regulation, maybe effective in preserving and even expanding the beta-cell mass. This assumption is based on data from in vitro and animal studies, with no clear demonstrations in humans. This class of drugs may represent an entirely new approach to the treatment of type 1 diabetes, focused on protection and preservation of beta-cells, an ideal complement to immune interventions inhibiting or modulating the pathogenetic autoimmune process. The ideal candidates for this treatment are patients at the time of clinical onset of type 1 diabetes or individuals with preclinical type 1 diabetes who still have a significant viable beta-cell mass. (J Clin Endocrinol Metab 95: 2607-2609, 2010)
引用
收藏
页码:2607 / 2609
页数:3
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