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神经退行性痴呆的基本病理学及其与最新分子影像学研究的相关性。

Basic pathologies of neurodegenerative dementias and their relevance for state-of-the-art molecular imaging studies.

作者信息

Drzezga Alexander

机构信息

Department of Nuclear Medicine, Klinikum rechts der Isar, Technische Universität München, Ismaninger Strasse 22, Munich, Germany.

出版信息

Eur J Nucl Med Mol Imaging. 2008 Mar;35 Suppl 1:S4-11. doi: 10.1007/s00259-007-0697-6.

Abstract

INTRODUCTION

Rising life-expectancy in the modern society has resulted in a rapidly growing prevalence of dementia, particularly of Alzheimer's disease (AD). Dementia turns into one of the most common age-related disorders with deleterious consequences for the concerned patients and their relatives, as well as worrying effects on the socio-economic systems. These facts justify strengthened scientific efforts to identify the pathologic origin of dementing disorders, to improve diagnosis, and to interfere therapeutically with the disease progression.

BASIC PATHOLOGIES

In the recent years, remarkable progress has been made concerning the identification of molecular mechanisms underlying the pathology of neurodegenerative disorders. Growing evidence indicates that a common basis of many neurodegenerative dementias can be found in increased production, misfolding and pathological aggregation of proteins, such as beta-amyloid, tau protein, a-synuclein, or the recently described ubiquitinated TDP-43. This progressive insight in pathological processes is paralleled by the development of new therapeutic approaches. However, the exact contribution or mechanism of different pathologies with regard to the development of disease is not yet sufficiently clear. Considerable overlap of pathologies has been documented in different types of clinically defined dementias post mortem, and it has been difficult to correlate post mortem histopathology data with disease-expression during life. Molecular imaging procedures may play a valuable role to circumvent this limitation.

RELEVANCE FOR IMAGING STUDIES

In general, methods of molecular imaging have recently experienced an impressive advance, with numerous new and improved technologies emerging. These exciting tools may play a key role in the future regarding the evaluation of pathomechanisms, preclinical evaluation of new diagnostic procedures in animal models, selection of patients for clinical trials, and therapy monitoring. In this overview, molecular key pathologies, which are currently regarded to be strongly associated with the development of different dementias, will be shortly summarized; it will also be discussed how state-of-the-art imaging technology can assist to visualize these processes now and in the future.

摘要

引言

现代社会预期寿命的不断提高导致痴呆症,尤其是阿尔茨海默病(AD)的患病率迅速上升。痴呆症已成为最常见的与年龄相关的疾病之一,给相关患者及其亲属带来有害后果,同时也对社会经济系统产生令人担忧的影响。这些事实证明有必要加强科学研究,以确定痴呆症的病理起源、改善诊断并对疾病进展进行治疗干预。

基本病理学

近年来,在确定神经退行性疾病病理学的分子机制方面取得了显著进展。越来越多的证据表明,许多神经退行性痴呆症的共同基础在于蛋白质(如β-淀粉样蛋白、tau蛋白、α-突触核蛋白或最近描述的泛素化TDP-43)的产生增加、错误折叠和病理性聚集。对病理过程的这种逐步深入了解与新治疗方法的发展相平行。然而,不同病理学在疾病发展中的具体作用或机制尚不完全清楚。不同类型临床定义的痴呆症死后病理重叠现象明显,且难以将死后组织病理学数据与生前疾病表现相关联。分子成像程序可能在克服这一局限性方面发挥重要作用。

对成像研究的意义

总体而言,分子成像方法近年来取得了令人瞩目的进展,涌现出众多新的和改进的技术。这些令人兴奋的工具在未来评估发病机制、动物模型中新诊断程序的临床前评估、临床试验患者的选择以及治疗监测方面可能发挥关键作用。在本综述中,将简要总结目前被认为与不同痴呆症发展密切相关的分子关键病理学;还将讨论先进的成像技术如何在现在和未来帮助可视化这些过程。

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