Basavaraju Manasa, de Lencastre Alexandre
Biomol Concepts. 2016 Aug 1;7(4):241-52. doi: 10.1515/bmc-2016-0014.
Alzheimer's disease (AD) is a progressive neurodegenerative disorder that accounts for the most cases of dementia. AD affects more than 25 million people globally and is predicted to affect nearly one in 85 people worldwide by 2050. AD is characterized by the accumulation of dense plaques of β-amyloid peptide (Aβ) and neurofibrillary tangles of hyperphosphorylated tau that cause impairment in memory, cognition, and daily activities. Although early-onset AD has been linked to several mutations, reliable genetic markers for late-onset AD are lacking. Further, the diagnosis of AD biomarkers has its limitations and cannot detect early-stage AD. The identification of accurate, early, and non-invasive biomarkers for AD is, therefore, an unmet challenge. Recently, microRNAs (miRNAs) have emerged as a novel class of gene regulatory elements with conserved roles in development and disease. Recent discoveries have uncovered roles of miRNAs in several model organisms during aging and have identified potential miRNAs biomarkers of AD. Here we will discuss this emerging field of miRNAs associated with AD and prospects for the future.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,占痴呆症病例的大多数。AD在全球影响着超过2500万人,预计到2050年全球每85人中就有近1人受其影响。AD的特征是β-淀粉样肽(Aβ)的致密斑块和过度磷酸化tau的神经原纤维缠结的积累,这些会导致记忆、认知和日常活动受损。虽然早发性AD与几种突变有关,但缺乏晚发性AD的可靠遗传标记。此外,AD生物标志物的诊断存在局限性,无法检测早期AD。因此,识别准确、早期和非侵入性的AD生物标志物是一个尚未解决的挑战。最近,微小RNA(miRNA)作为一类新型的基因调控元件出现,在发育和疾病中具有保守作用。最近的发现揭示了miRNA在几种模式生物衰老过程中的作用,并确定了AD的潜在miRNA生物标志物。在此,我们将讨论这个与AD相关的新兴miRNA领域及其未来前景。