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阿尔茨海默病是否为一种均质的疾病实体?

Is Alzheimer's disease a homogeneous disease entity?

机构信息

Tel-Aviv University Medical School, Tel-Aviv, Israel,

出版信息

J Neural Transm (Vienna). 2013 Oct;120(10):1475-7. doi: 10.1007/s00702-013-1060-7. Epub 2013 Aug 11.

DOI:10.1007/s00702-013-1060-7
PMID:23933662
Abstract

The epidemic proportions of dementia in old age are a cause of great concern for the medical profession and the society at large. It is customary to consider Alzheimer's disease (AD) as the most common cause of dementia, and vascular dementia (VaD) as being the second. This dichotomous view of a primary neurodegenerative disease as opposed to a disorder where extrinsic factors cause brain damage led to separate lines of research in these two entities. New biomarkers, particularly the introduction of modern neuroimaging and cerebrospinal fluid changes, have, in recent years, helped to identify anatomical and chemical changes of VaD and of AD. Nevertheless, there is a substantial difference between the two entities. While it is clear that VaD is a heterogeneous entity, AD is supposed to be a single disorder. Nobody attempts to use CADASIL as a template to develops treatment for sporadic VaD. On the other hand, early-onset AD is used to develop therapy for sporadic AD. This paper will discuss the problems relating to this false concept and its consequences.

摘要

老年痴呆症的流行程度是医学界和整个社会非常关注的问题。人们通常认为阿尔茨海默病(AD)是痴呆症最常见的原因,血管性痴呆(VaD)是第二常见的原因。这种将原发性神经退行性疾病与由外部因素引起的脑损伤区分开来的二分法观点导致了这两种疾病的研究方向分开。近年来,新的生物标志物,特别是现代神经影像学和脑脊液变化的引入,有助于识别 VaD 和 AD 的解剖和化学变化。然而,这两种疾病之间存在着很大的差异。虽然 VaD 显然是一种异质性疾病,但 AD 应该是一种单一的疾病。没有人试图用 CADASIL 作为模板来开发治疗散发性 VaD 的方法。另一方面,早发性 AD 则用于开发治疗散发性 AD 的方法。本文将讨论与这一错误概念及其后果相关的问题。

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Is Alzheimer's disease a homogeneous disease entity?阿尔茨海默病是否为一种均质的疾病实体?
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3
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引用本文的文献

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Beyond the usual suspects: multi-factorial computational models in the search for neurodegenerative disease mechanisms.超越常见的嫌疑对象:寻找神经退行性疾病机制的多因素计算模型。
Transl Psychiatry. 2024 Sep 23;14(1):386. doi: 10.1038/s41398-024-03073-w.
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Language and spatial dysfunction in Alzheimer disease with white matter thorn-shaped astrocytes.阿尔茨海默病伴白质刺状星形胶质细胞的语言和空间功能障碍。
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Fluid biomarker agreement and interrelation in dementia due to Alzheimer's disease.

本文引用的文献

1
Detection of β-amyloid oligomers as a predictor of neurological outcome after brain injury.检测β-淀粉样寡聚体作为脑损伤后神经功能预后的预测因子。
J Neurosurg. 2013 Jun;118(6):1336-42. doi: 10.3171/2013.2.JNS121771. Epub 2013 Mar 29.
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Cell signaling abnormalities may drive neurodegeneration in familial Alzheimer disease.细胞信号异常可能会导致家族性阿尔茨海默病中的神经退行性变。
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Encephalopathy: a vicious cascade following forebrain ischemia and hypoxia.
阿尔茨海默病所致痴呆的液体生物标志物的一致性和相关性。
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Multiple pathologies are common in Alzheimer patients in clinical trials.在临床试验中,阿尔茨海默病患者通常同时患有多种疾病。
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J Neurol Sci. 2012 Aug 15;319(1-2):124-9. doi: 10.1016/j.jns.2012.04.014. Epub 2012 May 8.
9
Autosomal-dominant Alzheimer's disease: a review and proposal for the prevention of Alzheimer's disease.常染色体显性阿尔茨海默病:综述及阿尔茨海默病预防建议。
Alzheimers Res Ther. 2011 Jan 6;3(1):1. doi: 10.1186/alzrt59.
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Decreased clearance of CNS beta-amyloid in Alzheimer's disease.阿尔茨海默病患者中枢神经系统β-淀粉样蛋白清除减少。
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