The Vicious Consequences of Chronic Kidney Disease on Cognitive Impairment and Alzheimer's Disease.

IF 4.1 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY ACS Chemical Neuroscience Pub Date : 2025-05-21 Epub Date: 2025-05-09 DOI:10.1021/acschemneuro.5c00050
Abhideep Roy, Rubina Roy, Pallab Bhattacharya, Anupom Borah
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Abstract

Chronic kidney disease (CKD) and Alzheimer's disease (AD) are two prevalent and debilitating conditions that frequently coexist, with CKD contributing to cognitive decline and potentially exacerbating AD pathology. In CKD, irreversible changes in the structure or function of the kidneys are observed, while AD is primarily marked by amyloid deposition and tau pathology. Both conditions involve complex and multifactorial pathophysiology affecting brain functioning, highlighting the need for comprehensive research to understand their potential crosstalk. This review articulates the possible molecular mechanisms underlying both diseases, focusing on key pathways, including oxidative stress, inflammation, vascular dysfunction, hypertension, and uremic toxin accumulation. These interconnected mechanisms suggest a potential bidirectional relationship where kidney dysfunction accelerates cognitive decline and vice versa. Additionally, we examine critical risk factors implicated in both CKD and AD, for instance, vitamin D deficiency, erythropoietin dysregulation, endothelin action, klotho gene expression, and the role of the extracellular vesicle, which may influence disease progression through their effects on the kidney and brain, influencing cognitive function. Further, we emphasized potential biomarkers that could aid in diagnosing and monitoring disease progression in these comorbid conditions, like amyloid beta, tau, homocysteine, cystatin C, creatinine, proteinuria, and estimated glomerular filtration rate. Lastly, the review highlights treatment strategies for managing CKD and AD concurrently, focusing on therapeutic approaches that address common pathophysiological mechanisms. These strategies not only aim to address the underlying causes of both conditions but also offer the potential to slow or even prevent the progression of cognitive impairment. Moreover, we recommend further research to refine these approaches, execute correlational studies on disease progression, and design clinical trials that address both conditions, aiming to establish effective, tailored treatments for this dual burden of disease.

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慢性肾脏疾病对认知障碍和阿尔茨海默病的恶性影响。
慢性肾脏疾病(CKD)和阿尔茨海默病(AD)是两种常见的使人衰弱的疾病,经常共存,CKD导致认知能力下降,并可能加剧AD病理。在CKD中,观察到肾脏结构或功能的不可逆变化,而AD主要以淀粉样蛋白沉积和tau病理为标志。这两种情况都涉及影响大脑功能的复杂和多因素病理生理,强调需要全面研究以了解它们潜在的相互作用。本文综述了这两种疾病可能的分子机制,重点讨论了氧化应激、炎症、血管功能障碍、高血压和尿毒症毒素积累等关键途径。这些相互关联的机制提示了一种潜在的双向关系,即肾功能障碍加速认知能力下降,反之亦然。此外,我们研究了CKD和AD的关键危险因素,例如维生素D缺乏、促红细胞生成素失调、内皮素作用、klotho基因表达和细胞外囊泡的作用,这些因素可能通过对肾脏和大脑的影响影响疾病进展,影响认知功能。此外,我们强调潜在的生物标志物可以帮助诊断和监测这些合并症的疾病进展,如淀粉样蛋白β、tau蛋白、同型半胱氨酸、胱抑素C、肌酐、蛋白尿和估计的肾小球滤过率。最后,综述强调了CKD和AD并发的治疗策略,重点是解决常见病理生理机制的治疗方法。这些策略不仅旨在解决这两种情况的潜在原因,而且还提供了减缓甚至预防认知障碍进展的潜力。此外,我们建议进一步研究以完善这些方法,对疾病进展进行相关研究,并设计针对这两种情况的临床试验,旨在为这种双重疾病负担建立有效的、量身定制的治疗方法。
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
ACS Chemical Neuroscience
ACS Chemical Neuroscience BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
9.20
自引率
4.00%
发文量
323
审稿时长
1 months
期刊介绍: ACS Chemical Neuroscience publishes high-quality research articles and reviews that showcase chemical, quantitative biological, biophysical and bioengineering approaches to the understanding of the nervous system and to the development of new treatments for neurological disorders. Research in the journal focuses on aspects of chemical neurobiology and bio-neurochemistry such as the following: Neurotransmitters and receptors Neuropharmaceuticals and therapeutics Neural development—Plasticity, and degeneration Chemical, physical, and computational methods in neuroscience Neuronal diseases—basis, detection, and treatment Mechanism of aging, learning, memory and behavior Pain and sensory processing Neurotoxins Neuroscience-inspired bioengineering Development of methods in chemical neurobiology Neuroimaging agents and technologies Animal models for central nervous system diseases Behavioral research
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