Diabetes and Metabolism, Bristol Medical School, University of Bristol, Level 2, Learning and Research, Southmead Hospital, Bristol, BS10 5NB, UK.
Curr Diab Rep. 2018 Sep 5;18(10):94. doi: 10.1007/s11892-018-1059-4.
Islet transplantation, an important approach to achieve insulin independence for individuals with type 1 diabetes, is limited by the lack of accurate biomarkers to track beta-cell death post islet infusion. In this review, we will discuss existing and recently described biomarkers.
As beta cells are killed by the immune system, fragments of beta cell-specific cell-free DNA and proteins are released into the periphery. Several different strategies to identify these fragments have been described. Some circulating, non-coding microRNAs, particularly miRNA-375 are also showing potential to reflect the rate of beta cell loss post-clinical islet transplantation. Recent advances in identifying accurate beta cell-specific biomarkers such as differentially methylated insulin cell-free DNA and circulating miRNA-375 may help predict clinical outcomes. More studies are required to examine the robustness of these biomarkers to detect chronic beta-cell loss in islet transplantation recipients.
胰岛移植是实现 1 型糖尿病患者胰岛素独立性的重要方法,但受到缺乏准确的生物标志物来跟踪胰岛输注后β细胞死亡的限制。在这篇综述中,我们将讨论现有的和最近描述的生物标志物。
随着β细胞被免疫系统杀死,β细胞特异性的无细胞 DNA 和蛋白质片段被释放到外周血中。已经描述了几种不同的策略来识别这些片段。一些循环的非编码 microRNAs,特别是 miRNA-375,也显示出反映临床胰岛移植后β细胞丢失率的潜力。最近在鉴定准确的β细胞特异性生物标志物方面的进展,如差异甲基化的胰岛素无细胞 DNA 和循环 miRNA-375,可能有助于预测临床结局。需要更多的研究来检验这些生物标志物检测胰岛移植受者慢性β细胞丢失的稳健性。