Alternative splicing and the aging brain in AfrAbia: New frontiers in dementia research

IF 2 Q3 NEUROSCIENCES
Suliyat Abiodun Aremu
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引用次数: 0

Abstract

AfrAbia (Sub-Saharan Africa and Arab world), is undergoing a significant demographic shift characterized by increased longevity and rising dementia rates. Despite this, molecular insights into brain aging in these regions, especially in RNA processing pathways like alternative splicing (AS), are virtually absent. AS promotes transcriptomic and proteomic complexity and is pivotal for brain function, with its dysregulation connected to neurodegenerative diseases such as Alzheimer’s disease (AD), frontotemporal dementia (FTD), and Parkinson’s disease (PD). However, current knowledge is overwhelmingly derived from Western populations, limiting global applicability. This perspective synthesizes the mechanisms and regulatory elements of AS, its role in aging and neurodegeneration, and emerging biomarkers and therapeutic strategies. Special attention is paid to ancestry-associated splicing variants and fluid biomarker development in AfrAbian cohorts. We argue for inclusive, population-specific molecular studies to bridge disparities in dementia diagnosis, treatment, and prevention.
选择性剪接和老化的大脑在非洲:痴呆研究的新领域
非洲(撒哈拉以南非洲和阿拉伯世界)正在经历重大的人口变化,其特点是寿命延长和痴呆症发病率上升。尽管如此,在这些区域,特别是在RNA加工途径如选择性剪接(AS)中,对大脑衰老的分子见解实际上是缺失的。AS促进转录组和蛋白质组的复杂性,对脑功能至关重要,其失调与阿尔茨海默病(AD)、额颞叶痴呆(FTD)和帕金森病(PD)等神经退行性疾病有关。然而,目前的知识绝大多数来自西方人群,限制了全球适用性。这一观点综合了AS的机制和调控因素,它在衰老和神经退行性变中的作用,以及新兴的生物标志物和治疗策略。特别关注非洲队列中与祖先相关的剪接变异和流体生物标志物的发展。我们主张进行包容性的、人群特异性的分子研究,以弥合痴呆诊断、治疗和预防方面的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
IBRO Neuroscience Reports
IBRO Neuroscience Reports Neuroscience-Neuroscience (all)
CiteScore
2.80
自引率
0.00%
发文量
99
审稿时长
14 weeks
期刊介绍:
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