Update: the role of epigenetics in the metabolic memory of diabetic complications.

Zhuo Chen, Vajir Malek, Rama Natarajan
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Abstract

Diabetes, a chronic disease characterized by hyperglycemia, is associated with significantly accelerated complications, including diabetic kidney disease (DKD), which increases morbidity and mortality. Hyperglycemia and other diabetes-related environmental factors such as overnutrition, sedentary lifestyles, and hyperlipidemia can induce epigenetic changes. Working alone or with genetic factors, these epigenetic changes that occur without alterations in the underlying DNA sequence, can alter the expression of pathophysiological genes and impair functions of associated target cells/organs, leading to diabetic complications like DKD. Notably, some hyperglycemia-induced epigenetic changes persist in target cells/tissues even after glucose normalization, leading to sustained complications despite glycemic control, so-called metabolic memory. Emerging evidence from in vitro and in vivo animal models and clinical trials with subjects with diabetes identified clear associations between metabolic memory and epigenetic changes including DNA methylation, histone modifications, chromatin structure, and noncoding RNAs at key loci. Targeting such persistent epigenetic changes and/or molecules regulated by them can serve as valuable opportunities to attenuate, or erase metabolic memory, which is crucial to prevent complication progression. Here, we review these cell/tissue-specific epigenetic changes identified to-date as related to diabetic complications, especially DKD, and the current status on targeting epigenetics to tackle metabolic memory. We also discuss limitations in current studies, including the need for more (epi)genome-wide studies, integrative analysis using multiple epigenetic marks and Omics datasets, and mechanistic evaluation of metabolic memory. Considering the tremendous technological advances in epigenomics, genetics, sequencing, and availability of genomic datasets from clinical cohorts, this field is likely to see considerable progress in the upcoming years.

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最新进展:表观遗传学在糖尿病并发症代谢记忆中的作用。
糖尿病是一种以高血糖为特征的慢性疾病,与包括糖尿病肾病(DKD)在内的并发症相关,这些并发症会大大加速糖尿病的进程,从而增加发病率和死亡率。高血糖和其他与糖尿病相关的环境因素(如营养过剩、久坐不动的生活方式和高脂血症)可诱发表观遗传变化。这些表观遗传学变化单独发生或与遗传因素一起发生时,其基本 DNA 序列不会发生改变,但会改变病理生理基因的表达,损害相关靶细胞/器官的功能,导致糖尿病并发症,如 DKD。值得注意的是,一些高血糖诱导的表观遗传学变化即使在血糖恢复正常后仍会在靶细胞/组织中持续存在,从而导致血糖控制后仍出现持续的并发症,即所谓的代谢记忆。来自体外、体内动物模型和糖尿病患者临床试验的新证据表明,代谢记忆与表观遗传学变化(包括 DNA 甲基化、组蛋白修饰、染色质结构和关键位点的非编码 RNA)之间存在明显关联。针对这些持久的表观遗传学变化和/或受其调控的分子,可以作为减弱或消除代谢记忆的宝贵机会,这对预防并发症的进展至关重要。在此,我们回顾了迄今为止发现的与糖尿病并发症(尤其是 DKD)相关的细胞/组织特异性表观遗传学变化,以及以表观遗传学为靶点解决代谢记忆问题的现状。我们还讨论了目前研究的局限性,包括需要进行更多(表)全基因组研究、使用多种表观遗传标记和 Omics 数据集进行综合分析,以及对代谢记忆进行机理评估。考虑到表观基因组学、遗传学、测序技术的巨大进步,以及临床队列基因组数据集的可用性,这一领域在未来几年可能会取得长足进步。
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