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胰岛细胞移植治疗 1 型糖尿病的生物标志物。

Biomarkers in Islet Cell Transplantation for Type 1 Diabetes.

机构信息

Diabetes and Metabolism, Bristol Medical School, University of Bristol, Level 2, Learning and Research, Southmead Hospital, Bristol, BS10 5NB, UK.

出版信息

Curr Diab Rep. 2018 Sep 5;18(10):94. doi: 10.1007/s11892-018-1059-4.

Abstract

PURPOSE OF REVIEW

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.

RECENT FINDINGS

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.

摘要

目的综述

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。

最近的发现

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1634/6132734/c7acf0dd7cca/11892_2018_1059_Fig1_HTML.jpg

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