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[阿尔茨海默病生物标志物的研究]

[Search of biological markers of Alzheimer's disease].

作者信息

Couderc R

机构信息

Service de biochimie, Hôpital Trousseau, 26, avenue du Dr-Arnold-Netter, 75571 Paris cedex 12, France.

出版信息

Ann Biol Clin (Paris). 2000 Sep-Oct;58(5):581-93.

PMID:11022101
Abstract

Peripheral markers for Alzheimer's disease are of interest to confirm the diagnosis, to perform epidemiological screening, to identify distinct groups of patients, to predict the outcome of the disease, to monitor its progression and its sensibility to treatment and to give help in performing studies on the relationship between brain and behaviour and on the pathophysiology of the Alzheimer's disease. The ideal biomarker for Alzheimer's disease should detect a fundamental feature of neuropathology and be validated in neuropathologically confirmed cases and be confirmed by at least two independent studies; should be as sensitive and specific than the clinical diagnosis (about 85% and 80%), reliable, reproducible, simple to perform, inexpensive and non invasive (studies on blood, urine, saliva, or buccal scrapings) or moderately invasive (skin, rectal biopsies, bone marrow samples, or cerebrospinal fluid). Such a marker has not yet been found. In this paper we present those markers which come closest to fulfilling criteria for a useful biomarker, keeping in mind that these criteria depends on what purpose it is used (screening, prediction, diagnosis, monitoring, pathophysiological studies.) and that the finding of a good marker depends on the understanding of the disease.

摘要

阿尔茨海默病的外周标志物对于确诊、进行流行病学筛查、识别不同患者群体、预测疾病转归、监测疾病进展及其对治疗的敏感性,以及辅助开展关于大脑与行为关系及阿尔茨海默病病理生理学的研究都具有重要意义。阿尔茨海默病的理想生物标志物应能检测神经病理学的基本特征,并在经神经病理学确诊的病例中得到验证,且至少有两项独立研究予以证实;应与临床诊断一样敏感和特异(约85%和80%),可靠、可重复、操作简便、成本低廉且非侵入性(针对血液、尿液、唾液或口腔刮片的研究)或中度侵入性(皮肤、直肠活检、骨髓样本或脑脊液)。目前尚未找到这样一种标志物。在本文中,我们介绍了那些最接近满足有用生物标志物标准的标志物,同时要记住这些标准取决于其使用目的(筛查、预测、诊断、监测、病理生理学研究),并且找到一个好的标志物取决于对该疾病的理解。

相似文献

1
[Search of biological markers of Alzheimer's disease].[阿尔茨海默病生物标志物的研究]
Ann Biol Clin (Paris). 2000 Sep-Oct;58(5):581-93.
2
Consensus report of the Working Group on: "Molecular and Biochemical Markers of Alzheimer's Disease". The Ronald and Nancy Reagan Research Institute of the Alzheimer's Association and the National Institute on Aging Working Group.“阿尔茨海默病的分子和生化标志物”工作组共识报告。阿尔茨海默病协会罗纳德和南希·里根研究所与美国国立衰老研究所工作组。
Neurobiol Aging. 1998 Mar-Apr;19(2):109-16.
3
Cerebrospinal fluid beta-amyloid1-42 and tau in control subjects at risk for Alzheimer's disease: the effect of APOE epsilon4 allele.阿尔茨海默病风险对照受试者的脑脊液β淀粉样蛋白1-42和tau蛋白:APOE ε4等位基因的影响
Biol Psychiatry. 2004 Nov 1;56(9):670-6. doi: 10.1016/j.biopsych.2004.07.021.
4
[The progress of Alzheimer's disease research biomarkers--sensitivity and specificity].[阿尔茨海默病研究生物标志物的进展——敏感性和特异性]
Rinsho Shinkeigaku. 2000 Dec;40(12):1234-6.
5
Value of CSF beta-amyloid1-42 and tau as predictors of Alzheimer's disease in patients with mild cognitive impairment.脑脊液β-淀粉样蛋白1-42和tau蛋白作为轻度认知障碍患者阿尔茨海默病预测指标的价值
Mol Psychiatry. 2004 Jul;9(7):705-10. doi: 10.1038/sj.mp.4001473.
6
CSF beta-amyloid 1-42 and tau in Tunisian patients with Alzheimer's disease: the effect of APOE epsilon4 allele.突尼斯阿尔茨海默病患者脑脊液中的β-淀粉样蛋白1-42和tau蛋白:APOE ε4等位基因的影响
Neurosci Lett. 2008 Aug 1;440(2):145-9. doi: 10.1016/j.neulet.2008.05.076. Epub 2008 May 24.
7
No association of CSF biomarkers with APOEepsilon4, plaque and tangle burden in definite Alzheimer's disease.在确诊的阿尔茨海默病中,脑脊液生物标志物与APOEε4、斑块和缠结负荷之间无关联。
Brain. 2007 Sep;130(Pt 9):2320-6. doi: 10.1093/brain/awm136. Epub 2007 Jun 22.
8
[Interest of CSF beta-amyloid1-42 and t-tau protein level determinations for the diagnosis of Alzheimer's disease].[脑脊液β-淀粉样蛋白1-42和总tau蛋白水平测定对阿尔茨海默病诊断的意义]
Ann Biol Clin (Paris). 2008 Sep-Oct;66(5):531-5. doi: 10.1684/abc.2008.0265.
9
[Alzheimer's disease as brain amyloidosis: diagnosis using cerebrospinal fluid abeta and tau].[作为脑淀粉样变性的阿尔茨海默病:使用脑脊液β淀粉样蛋白和tau蛋白进行诊断]
Rinsho Byori. 2006 May;54(5):503-8.
10
Subgroups of Alzheimer's disease based on cerebrospinal fluid molecular markers.基于脑脊液分子标志物的阿尔茨海默病亚组
Ann Neurol. 2005 Nov;58(5):748-57. doi: 10.1002/ana.20639.

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