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本文引用的文献

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Biomarkers of Alzheimer disease in plasma.血浆中阿尔茨海默病的生物标志物。
NeuroRx. 2004 Apr;1(2):226-34. doi: 10.1602/neurorx.1.2.226.
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Mild cognitive impairment--beyond controversies, towards a consensus: report of the International Working Group on Mild Cognitive Impairment.轻度认知障碍——超越争议,走向共识:轻度认知障碍国际工作组报告
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CSF biomarkers for mild cognitive impairment.用于轻度认知障碍的脑脊液生物标志物。
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Mild cognitive impairment as a diagnostic entity.轻度认知障碍作为一种诊断实体。
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The current status of Alzheimer's disease genetics: what do we tell the patients?阿尔茨海默病遗传学的现状:我们该如何告知患者?
Pharmacol Res. 2004 Oct;50(4):385-96. doi: 10.1016/j.phrs.2003.11.018.
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Looking backward to move forward: early detection of neurodegenerative disorders.回首往昔,展望未来:神经退行性疾病的早期检测
Science. 2003 Oct 31;302(5646):830-4. doi: 10.1126/science.1090349.
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Pathology and pathways of Alzheimer's disease with an update on new developments in treatment.阿尔茨海默病的病理学与发病机制以及治疗新进展
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Excitotoxic and excitoprotective mechanisms: abundant targets for the prevention and treatment of neurodegenerative disorders.兴奋性毒性和兴奋性保护机制:预防和治疗神经退行性疾病的丰富靶点。
Neuromolecular Med. 2003;3(2):65-94. doi: 10.1385/NMM:3:2:65.
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Unfolding the role of protein misfolding in neurodegenerative diseases.揭示蛋白质错误折叠在神经退行性疾病中的作用。
Nat Rev Neurosci. 2003 Jan;4(1):49-60. doi: 10.1038/nrn1007.
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Comparison of automated and manual MRI volumetry of hippocampus in normal aging and dementia.正常衰老和痴呆症中海马体的自动与手动MRI容积测量比较。
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阿尔茨海默病神经影像学计划。

The Alzheimer's disease neuroimaging initiative.

作者信息

Mueller Susanne G, Weiner Michael W, Thal Leon J, Petersen Ronald C, Jack Clifford, Jagust William, Trojanowski John Q, Toga Arthur W, Beckett Laurel

机构信息

Department of Radiology, University of California, San Francisco, CA, USA.

出版信息

Neuroimaging Clin N Am. 2005 Nov;15(4):869-77, xi-xii. doi: 10.1016/j.nic.2005.09.008.

DOI:10.1016/j.nic.2005.09.008
PMID:16443497
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2376747/
Abstract

With increasing life expectancy in developed countries, the incidence of Alzheimer's disease (AD) and its socioeconomic impact are growing. Increasing knowledge of the mechanisms of AD facilitates the development of treatment strategies aimed at slowing down or preventing neuronal death. AD treatment trials using clinical outcome measures require long observation times and large patient samples. There is increasing evidence that neuroimaging and cerebrospinal fluid and blood biomarkers may provide information that may reduce sample sizes and observation periods. The Alzheimer's Disease Neuroimaging Initiative will help identify clinical, neuroimaging, and biomarker outcome measures that provide the highest power for measurement of longitudinal changes and for prediction of transitions.

摘要

随着发达国家人均寿命的延长,阿尔茨海默病(AD)的发病率及其社会经济影响正在不断增加。对AD发病机制的深入了解有助于制定旨在减缓或预防神经元死亡的治疗策略。使用临床结局指标的AD治疗试验需要较长的观察时间和大量的患者样本。越来越多的证据表明,神经影像学、脑脊液和血液生物标志物可能提供有助于减少样本量和观察期的信息。阿尔茨海默病神经影像学计划将有助于确定临床、神经影像学和生物标志物结局指标,这些指标在测量纵向变化和预测病情转变方面具有最高的效能。