Aremu Suliyat Abiodun
Department of Physiology, Ladoke Akintola University of Technology, Ogbomoso, Nigeria.
IBRO Neurosci Rep. 2025 Jun 16;19:101-109. doi: 10.1016/j.ibneur.2025.06.006. eCollection 2025 Dec.
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.
非洲阿拉伯地区(撒哈拉以南非洲和阿拉伯世界)正在经历重大的人口结构转变,其特点是寿命延长和痴呆症发病率上升。尽管如此,对这些地区大脑衰老的分子见解,尤其是在诸如可变剪接(AS)等RNA加工途径方面,几乎不存在。可变剪接促进转录组和蛋白质组的复杂性,对大脑功能至关重要,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,限制了其全球适用性。这篇综述综合了可变剪接的机制和调控元件、其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。特别关注非洲阿拉伯人群队列中与祖先相关的剪接变体和液体生物标志物的开发。我们主张进行包容性的、针对特定人群的分子研究,以弥合痴呆症诊断、治疗和预防方面的差距。