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Testing Episodic Memory in Elderly Subjects: Not as Simple as It Looks.测试老年受试者的情景记忆:并非看上去那么简单。
Dement Geriatr Cogn Dis Extra. 2019 Jun 18;9(2):207-216. doi: 10.1159/000499836. eCollection 2019 May-Aug.
2
NIA-AA Research Framework: Toward a biological definition of Alzheimer's disease.NIA-AA 研究框架:迈向阿尔茨海默病的生物学定义。
Alzheimers Dement. 2018 Apr;14(4):535-562. doi: 10.1016/j.jalz.2018.02.018.
3
Does MRI Increase the Diagnostic Confidence of Physicians in an Outpatient Memory Clinic.磁共振成像(MRI)能否提高门诊记忆诊所医生的诊断信心?
Dement Geriatr Cogn Dis Extra. 2016 Jun 25;6(2):242-51. doi: 10.1159/000445711. eCollection 2016 May-Aug.
4
Matrix Metalloproteinases in Alzheimer's Disease and Concurrent Cerebral Microbleeds.阿尔茨海默病与并发脑微出血中的基质金属蛋白酶
J Alzheimers Dis. 2015;48(3):711-20. doi: 10.3233/JAD-143186.
5
Performance and complications of lumbar puncture in memory clinics: Results of the multicenter lumbar puncture feasibility study.在记忆门诊行腰椎穿刺的表现和并发症:多中心腰椎穿刺可行性研究的结果。
Alzheimers Dement. 2016 Feb;12(2):154-163. doi: 10.1016/j.jalz.2015.08.003. Epub 2015 Sep 11.
6
Cerebrospinal fluid tau and amyloid-β1-42 in patients with dementia.患者脑脊液中的 tau 和淀粉样蛋白-β1-42。
Brain. 2015 Sep;138(Pt 9):2716-31. doi: 10.1093/brain/awv181. Epub 2015 Jun 30.
7
Advancing research diagnostic criteria for Alzheimer's disease: the IWG-2 criteria.推进阿尔茨海默病研究诊断标准:IWG-2 标准。
Lancet Neurol. 2014 Jun;13(6):614-29. doi: 10.1016/S1474-4422(14)70090-0.
8
The cerebrospinal fluid "Alzheimer profile": easily said, but what does it mean?脑脊液“阿尔茨海默病特征”:说来容易,但它到底意味着什么?
Alzheimers Dement. 2014 Nov;10(6):713-723.e2. doi: 10.1016/j.jalz.2013.12.023. Epub 2014 Apr 8.
9
Quantification of clusterin in paired cerebrospinal fluid and plasma samples.配对的脑脊液和血浆样本中簇集素的定量分析。
Ann Clin Biochem. 2014 Sep;51(Pt 5):557-67. doi: 10.1177/0004563213503456. Epub 2013 Oct 21.
10
Discriminatory and predictive capabilities of enzyme-linked immunosorbent assay and multiplex platforms in a longitudinal Alzheimer's disease study.酶联免疫吸附测定和多重平台在一项阿尔茨海默病纵向研究中的判别和预测能力。
Alzheimers Dement. 2013 May;9(3):276-83. doi: 10.1016/j.jalz.2012.01.004. Epub 2012 Oct 27.

再次探讨当地医院记忆诊所脑脊液生物标志物的诊断影响。

Diagnostic Impact of CSF Biomarkers in a Local Hospital Memory Clinic Revisited.

机构信息

Department of Geriatric Medicine, NoordWest Hospital Group, Alkmaar, The Netherlands,

Department of Geriatric Medicine, NoordWest Hospital Group, Alkmaar, The Netherlands.

出版信息

Dement Geriatr Cogn Disord. 2020;49(1):2-7. doi: 10.1159/000506332. Epub 2020 Mar 30.

DOI:10.1159/000506332
PMID:32224618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7592944/
Abstract

BACKGROUND/AIMS: Research guidelines on predicting and diagnosing Alzheimer's disease (AD) acknowledge cerebrospinal fluid (CSF) levels as pivotal biomarkers. We studied the usefulness of CSF biomarkers in the diagnostic workup of patients in a geriatric outpatient memory clinic of a community-based hospital, attempted to determine a cutoff age for the use of CSF biomarkers in this group of patients, and compared the total τ/Aβ ratio as an alternative CSF diagnostic rule with the usual rules for interpreting CSF levels.

METHODS

This was a prospective study of consecutively referred patients. Inclusion criteria were described on the basis of previous study results in the same setting. The CSF tool was applied either to differentiate between AD and no AD or to increase certainty having made the diagnosis of AD. Clinicians were asked to judge whether the CSF results were helpful to them or not.

RESULTS

The reasons to use the CSF tool in the diagnostic workup were in 78/106 patients to decide between the diagnosis "AD" and "no AD" and in 28/106 patients to increase the certainty regarding the diagnosis. In 75% of cases the CSF levels were considered diagnostically helpful to the clinicians. Results in the present setting suggest 65 years as the cutoff age to use CSF as a diagnostic tool. The sensitivity and specificity of the total τ/Aβ ratio using the clinical diagnosis as the gold standard were at least as good as the usual categorization rule.

CONCLUSIONS

Our study results corroborate earlier findings that the CSF tool is of added value to the diagnostic workup in daily clinical practice outside tertiary referral centers. CSF levels can best be used in patients under 66 years of age. Given the limited use of this tool in settings outside research facilities, we recommend that the usefulness of CSF biomarkers is studied in a multicenter study. When in the future CSF levels can be reliably measured in plasma, this may become even more relevant.

摘要

背景/目的:预测和诊断阿尔茨海默病(AD)的研究指南承认脑脊液(CSF)水平是关键的生物标志物。我们研究了在社区医院老年门诊记忆诊所的患者的诊断工作中 CSF 生物标志物的有用性,尝试确定在该组患者中使用 CSF 生物标志物的截止年龄,并比较总 τ/Aβ 比值作为替代 CSF 诊断规则与解释 CSF 水平的常用规则。

方法

这是一项连续转诊患者的前瞻性研究。纳入标准是根据同一环境中先前的研究结果描述的。CSF 工具用于区分 AD 和非 AD,或增加 AD 诊断的确定性。临床医生被要求判断 CSF 结果是否对他们有帮助。

结果

在诊断工作中使用 CSF 工具的原因是在 106 名患者中的 78 名患者中决定“AD”和“非 AD”之间的诊断,在 106 名患者中的 28 名患者中增加对诊断的确定性。在 75%的情况下,CSF 水平被认为对临床医生具有诊断帮助。本研究结果表明,65 岁是将 CSF 作为诊断工具的截止年龄。使用临床诊断作为金标准时,总 τ/Aβ 比值的敏感性和特异性至少与常规分类规则一样好。

结论

我们的研究结果证实了 CSF 工具在三级转诊中心以外的日常临床实践中对诊断工作具有附加价值的早期发现。CSF 水平最适合年龄在 66 岁以下的患者使用。鉴于该工具在研究设施外的使用有限,我们建议在多中心研究中研究 CSF 生物标志物的有用性。当将来能够在血浆中可靠地测量 CSF 水平时,这可能会变得更加相关。