了解生物标志物和治疗神经系统疾病的进展--小脑功能障碍的作用和新兴疗法。

IF 12.5 1区 医学 Q1 CELL BIOLOGY
Azhagu Madhavan Sivalingam
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引用次数: 0

摘要

人们越来越认识到,小脑功能障碍是阿尔茨海默病(AD)、帕金森病(PD)和肌萎缩侧索硬化症(ALS)等多种神经系统疾病的关键因素。研究发现,在阿尔茨海默病和多系统萎缩等疾病中,小脑萎缩的模式各不相同,对小鼠的研究也强调了小脑萎缩对运动控制和认知功能的影响。对自闭症谱系障碍(ASD)的新兴研究发现了一些关键靶点,如趋化因子受体和 ZIC 家族基因水平的升高。包括脑脊液(CSF)在内的生物标记物、遗传标记物以及人工智能和生物信息学的进步,正在加强神经退行性疾病的早期诊断和个性化治疗。显著的进步包括改进的诊断工具、基因疗法和新型临床试验。尽管取得了进展,但血脑屏障和神经炎症等挑战依然存在。目前针对AD、PD、HD和ALS的疗法,包括反义寡核苷酸和干细胞疗法,都显示出治疗前景,但仍需进一步研究。整合诊断方法和创新疗法的综合方法对于有效管理和改善患者预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advances in understanding biomarkers and treating neurological diseases – Role of the cerebellar dysfunction and emerging therapies
Cerebellar dysfunction is increasingly recognized as a critical factor in various neurological diseases, including Alzheimer's disease (AD), Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS). Research has revealed distinct cerebellar atrophy patterns in conditions such as AD and multiple system atrophy, and studies in mice have highlighted its impact on motor control and cognitive functions. Emerging research into autism spectrum disorder (ASD) has identified key targets, such as elevated levels of chemokine receptors and ZIC family genes. Biomarkers, including cerebrospinal fluid (CSF), genetic markers, and advances in AI and bioinformatics, are enhancing early diagnosis and personalized treatment across neurodegenerative disorders. Notable advancements include improved diagnostic tools, gene therapy, and novel clinical trials. Despite progress, challenges such as the bloodbrain barrier and neuroinflammation persist. Current therapies for AD, PD, HD, and ALS, including antisense oligonucleotides and stem cell treatments, show promise but require further investigation. A comprehensive approach that integrates diagnostic methods and innovative therapies is essential for effective management and improved patient outcomes.
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来源期刊
Ageing Research Reviews
Ageing Research Reviews 医学-老年医学
CiteScore
19.80
自引率
2.30%
发文量
216
审稿时长
55 days
期刊介绍: With the rise in average human life expectancy, the impact of ageing and age-related diseases on our society has become increasingly significant. Ageing research is now a focal point for numerous laboratories, encompassing leaders in genetics, molecular and cellular biology, biochemistry, and behavior. Ageing Research Reviews (ARR) serves as a cornerstone in this field, addressing emerging trends. ARR aims to fill a substantial gap by providing critical reviews and viewpoints on evolving discoveries concerning the mechanisms of ageing and age-related diseases. The rapid progress in understanding the mechanisms controlling cellular proliferation, differentiation, and survival is unveiling new insights into the regulation of ageing. From telomerase to stem cells, and from energy to oxyradical metabolism, we are witnessing an exciting era in the multidisciplinary field of ageing research. The journal explores the cellular and molecular foundations of interventions that extend lifespan, such as caloric restriction. It identifies the underpinnings of manipulations that extend lifespan, shedding light on novel approaches for preventing age-related diseases. ARR publishes articles on focused topics selected from the expansive field of ageing research, with a particular emphasis on the cellular and molecular mechanisms of the aging process. This includes age-related diseases like cancer, cardiovascular disease, diabetes, and neurodegenerative disorders. The journal also covers applications of basic ageing research to lifespan extension and disease prevention, offering a comprehensive platform for advancing our understanding of this critical field.
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