神经退行性疾病的新时代。新方法的基础]。

IF 0.8 4区 医学 Q4 CLINICAL NEUROLOGY
G García-Ribas, P Garay-Albizuri, E S Stiauren-Fernández, F Pérez-Trapote, M A Zea-Sevilla
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引用次数: 0

摘要

通过检测与错误折叠蛋白疾病相关的病理生理和分子过程的生物标志物,使描述这些过程的自然历史成为可能。绝大多数蛋白质错误折叠疾病都有一个延长的临床前阶段,其中生物学变化是专利的。临床表现(即表型)与潜在病理没有明确的对应关系,尽管病理同义词已被用于临床综合征的描述,这有利于诊断的不准确性。为了进行适当的临床治疗,我们必须了解目前定义最常见的神经退行性过程的三个层面。诊断的准确性将是旨在改变脑蛋白错误折叠疾病过程的新疗法的先决条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The new age of neurodegenerative diseases. The basis of the new approaches].

The detection by biomarkers of the pathophysiological and molecular processes involved in misfolding protein diseases making it possible to delineate the natural history of these processes. The great majority of protein misfolding diseases have a prolonged preclinical phase, in which the biological changes are patent. The clinical manifestations (i.e., phenotypes) do not have a univocal correspondence with the underlying pathology, despite the fact that pathological eponyms have been used for the description of the clinical syndromes, which has favored diagnostic inaccuracy. In order to perform an adequate clinical management, we must know the 3 planes that currently define the most common neurodegenerative processes. Diagnostic accuracy will be a prerequisite for new therapies aimed at modifying the course of brain protein misfolding diseases.

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来源期刊
Revista de neurologia
Revista de neurologia 医学-临床神经学
CiteScore
2.50
自引率
8.30%
发文量
117
审稿时长
3-8 weeks
期刊介绍: Revista de Neurología fomenta y difunde el conocimiento generado en lengua española sobre neurociencia, tanto clínica como experimental.
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