Alzheimer's Disease and Vascular Dementia, Connecting and Differentiating Features.

Mikołaj Hurła, Natalia Banaszek, Wojciech Kozubski, Jolanta Dorszewska
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Abstract

Alzheimer's disease (AD) and vascular dementia (VD) are the leading causes of dementia, presenting a significant challenge in differential diagnosis. While their clinical presentations can overlap, their underlying pathologies are distinct. AD is characterized by the accumulation of amyloid plaques and neurofibrillary tangles, leading to progressive neurodegeneration. VD, on the other hand, arises from cerebrovascular insults that disrupt blood flow to the brain, causing neuronal injury and cognitive decline. Despite distinct etiologies, AD and VD share common risk factors such as hypertension, diabetes, and hyperlipidemia. Recent research suggests a potential role for oral microbiota in both diseases, warranting further investigation. The diagnostic dilemma lies in the significant overlap of symptoms including memory loss, executive dysfunction, and personality changes. The absence of definitive biomarkers and limitations of current neuroimaging techniques necessitate a multi-modal approach integrating clinical history, cognitive assessment, and neuroimaging findings. Promising avenues for improved diagnosis include the exploration of novel biomarkers like inflammatory markers, MMPs, and circulating microRNAs. Additionally, advanced neuroimaging techniques hold promise in differentiating AD and VD by revealing characteristic cerebrovascular disease patterns and brain atrophy specific to each condition. By elucidating the complexities underlying AD and VD, we can refine diagnostic accuracy and optimize treatment strategies for this ever-growing patient population. Future research efforts should focus on identifying disease-specific biomarkers and developing more effective neuroimaging methods to achieve a definitive diagnosis and guide the development of targeted therapies.

阿尔茨海默病和血管性痴呆,联系和区别特征。
阿尔茨海默病(AD)和血管性痴呆(VD)是痴呆症的主要病因,给鉴别诊断带来了巨大挑战。虽然它们的临床表现可能重叠,但其根本病理却截然不同。多发性硬化症的特征是淀粉样蛋白斑块和神经纤维缠结的累积,导致进行性神经变性。而脑血管病则是由于脑血管损伤导致脑血流中断,造成神经元损伤和认知能力下降。尽管病因不同,但注意力缺失症和视网膜病变具有共同的风险因素,如高血压、糖尿病和高脂血症。最近的研究表明,口腔微生物群在这两种疾病中都有潜在作用,值得进一步研究。诊断上的难题在于记忆力减退、执行功能障碍和人格改变等症状的显著重叠。由于缺乏明确的生物标志物,且目前的神经成像技术存在局限性,因此有必要采用多模式方法,将临床病史、认知评估和神经成像结果结合起来。改进诊断的可行途径包括探索新型生物标志物,如炎症标志物、MMPs 和循环 microRNAs。此外,先进的神经影像学技术通过揭示每种疾病特有的脑血管疾病模式和脑萎缩,有望区分出 AD 和 VD。通过阐明 AD 和 VD 背后的复杂性,我们可以提高诊断的准确性,并优化针对这一不断增长的患者群体的治疗策略。未来的研究工作应侧重于确定疾病特异性生物标志物和开发更有效的神经影像学方法,以实现明确诊断并指导靶向疗法的开发。
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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