Minniakhmetov Ildar, Yalaev Bulat, Khusainova Rita, Bondarenko Ekaterina, Melnichenko Galina, Dedov Ivan, Mokrysheva Natalia
Endocrinology Research Centre, Dmitry Ulyanov Street, 11, 117292 Moscow, Russia.
Biomedicines. 2024 Feb 8;12(2):399. doi: 10.3390/biomedicines12020399.
Omics technologies accumulated an enormous amount of data that advanced knowledge about the molecular pathogenesis of type 1 diabetes mellitus and identified a number of fundamental problems focused on the transition to personalized diabetology in the future. Among them, the most significant are the following: (1) clinical and genetic heterogeneity of type 1 diabetes mellitus; (2) the prognostic significance of DNA markers beyond the genes; (3) assessment of the contribution of a large number of DNA markers to the polygenic risk of disease progress; (4) the existence of ethnic population differences in the distribution of frequencies of risk alleles and genotypes; (5) the infancy of epigenetic research into type 1 diabetes mellitus. Disclosure of these issues is one of the priorities of fundamental diabetology and practical healthcare. The purpose of this review is the systemization of the results of modern molecular genetic, transcriptomic, and epigenetic investigations of type 1 diabetes mellitus in general, as well as its individual forms. The paper summarizes data on the role of risk haplotypes and a number of other candidate genes and loci, identified through genome-wide association studies, in the development of this disease and in alterations in T cell signaling. In addition, this review assesses the contribution of differential DNA methylation and the role of microRNAs in the formation of the molecular pathogenesis of type 1 diabetes mellitus, as well as discusses the most currently central trends in the context of early diagnosis of type 1 diabetes mellitus.
组学技术积累了大量数据,这些数据推动了对1型糖尿病分子发病机制的认识,并确定了一些未来向个性化糖尿病学转变所关注的基本问题。其中,最重要的问题如下:(1)1型糖尿病的临床和遗传异质性;(2)基因以外DNA标记的预后意义;(3)评估大量DNA标记对疾病进展多基因风险的贡献;(4)风险等位基因和基因型频率分布存在种族群体差异;(5)1型糖尿病表观遗传学研究尚处于起步阶段。揭示这些问题是基础糖尿病学和实际医疗保健的优先事项之一。本综述的目的是对1型糖尿病及其个体形式的现代分子遗传学、转录组学和表观遗传学研究结果进行系统化梳理。本文总结了通过全基因组关联研究确定的风险单倍型以及其他一些候选基因和基因座在该疾病发展和T细胞信号改变中的作用的数据。此外,本综述评估了差异DNA甲基化的作用以及微小RNA在1型糖尿病分子发病机制形成中的作用,并讨论了1型糖尿病早期诊断背景下当前最核心的趋势。