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阿尔茨海默病。

Alzheimer's disease.

机构信息

Department of Neurology & Alzheimer Center, VU University Medical Center, Amsterdam, Netherlands.

Clinical Neurochemistry Lab, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

出版信息

Lancet. 2016 Jul 30;388(10043):505-17. doi: 10.1016/S0140-6736(15)01124-1. Epub 2016 Feb 24.

Abstract

Although the prevalence of dementia continues to increase worldwide, incidence in the western world might have decreased as a result of better vascular care and improved brain health. Alzheimer's disease, the most prevalent cause of dementia, is still defined by the combined presence of amyloid and tau, but researchers are gradually moving away from the simple assumption of linear causality as proposed in the original amyloid hypothesis. Age-related, protective, and disease-promoting factors probably interact with the core mechanisms of the disease. Amyloid β42, and tau proteins are established core cerebrospinal biomarkers; novel candidate biomarkers include amyloid β oligomers and synaptic markers. MRI and fluorodeoxyglucose PET are established imaging techniques for diagnosis of Alzheimer's disease. Amyloid PET is gaining traction in the clinical arena, but validity and cost-effectiveness remain to be established. Tau PET might offer new insights and be of great help in differential diagnosis and selection of patients for trials. In the search for understanding the disease mechanism and keys to treatment, research is moving increasingly into the earliest phase of disease. Preclinical Alzheimer's disease is defined as biomarker evidence of Alzheimer's pathological changes in cognitively healthy individuals. Patients with subjective cognitive decline have been identified as a useful population in whom to look for preclinical Alzheimer's disease. Moderately positive results for interventions targeting several lifestyle factors in non-demented elderly patients and moderately positive interim results for lowering amyloid in pre-dementia Alzheimer's disease suggest that, ultimately, there will be a future in which specific anti-Alzheimer's therapy will be combined with lifestyle interventions targeting general brain health to jointly combat the disease. In this Seminar, we discuss the main developments in Alzheimer's research.

摘要

尽管痴呆症的患病率在全球范围内持续上升,但由于血管护理的改善和大脑健康状况的改善,西方世界的发病率可能已经下降。阿尔茨海默病是痴呆症最常见的病因,其定义仍然是淀粉样蛋白和tau 的共同存在,但研究人员正在逐渐摆脱原淀粉样蛋白假说中提出的简单线性因果关系假设。与年龄相关的、保护性的和促进疾病的因素可能与疾病的核心机制相互作用。淀粉样蛋白 β42 和 tau 蛋白是已确立的核心脑脊液生物标志物;新的候选生物标志物包括淀粉样蛋白 β 寡聚物和突触标志物。磁共振成像(MRI)和氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)是诊断阿尔茨海默病的既定影像学技术。淀粉样蛋白 PET 在临床领域越来越受欢迎,但有效性和成本效益仍有待确定。tau PET 可能提供新的见解,并有助于鉴别诊断和选择临床试验患者。在寻找理解疾病机制和治疗方法的过程中,研究越来越多地进入疾病的早期阶段。临床前阿尔茨海默病定义为认知健康个体中存在阿尔茨海默病病理变化的生物标志物证据。已经确定主观认知下降的患者是寻找临床前阿尔茨海默病的有用人群。针对非痴呆老年患者的几种生活方式因素的干预措施的适度阳性结果以及在轻度认知障碍阿尔茨海默病患者中降低淀粉样蛋白的适度阳性中期结果表明,最终将有一种未来,其中针对特定的抗阿尔茨海默病治疗将与针对大脑整体健康的生活方式干预措施相结合,共同对抗疾病。在本次研讨会上,我们将讨论阿尔茨海默病研究的主要进展。

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