ArticleEuropean archives of psychiatry and clinical neuroscience2016
Mapping CSF biomarker profiles onto NIA-AA guidelines for Alzheimer's disease.
Article in European archives of psychiatry and clinical neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 15 citations in OpenAlex.
- Agreement of cerebrospinal fluid biomarkers and amyloid-PET in a multicenter study.European archives of psychiatry and clinical neuroscience · 2025Article
- Unsupervised [European journal of nuclear medicine and molecular imaging · 2023Article
- Clinical characteristics of patients with suspected Alzheimer's disease within a CSF Aß-ratio grey zone.Neurological research and practice · 2023Article
- Validation of the Alzheimer Disease Dementia Conversion-Related Pattern as an ATN Biomarker of Neurodegeneration.Neurology · 2021Article
- Plasma levels of soluble amyloid precursor protein β in symptomatic Alzheimer's disease.European archives of psychiatry and clinical neuroscience · 2018Article
- Fluid and imaging biomarkers for Alzheimer's disease: Where we stand and where to head to.Experimental gerontology · 2018Review
- Fluid biomarker agreement and interrelation in dementia due to Alzheimer's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2018Article
- Conflicting cerebrospinal fluid biomarkers and progression to dementia due to Alzheimer's disease.Alzheimer's research & therapy · 2016Article
- Searching biomarkers for mental disorders-lessons from Alzheimer's disease.European archives of psychiatry and clinical neuroscience · 2016Article
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Authors and funding
15 authors at 3 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The National Institute on Aging-Alzheimer's Association (NIA-AA) guidelines for Alzheimer's disease (AD) propose the categorization of individuals according to their biomarker constellation. Though the NIA-AA criteria for preclinical AD and AD dementia have already been applied in conjunction with imaging AD biomarkers, the application of the criteria using comprehensive cerebrospinal fluid (CSF) biomarker information has not been thoroughly studied yet. The study included a monocentric cohort with healthy (N = 41) and disease (N = 22) controls and patients with AD dementia (N = 119), and a multicentric sample with healthy controls (N = 116) and patients with AD dementia (N = 102). The CSF biomarkers β-amyloid 1-42, total tau, and phosphorylated tau at threonine 181 were measured with commercially available assays. Biomarker values were trichotomized into positive for AD, negative, or borderline. In controls the presence of normal CSF profiles varied between 13.6 and 25.4 % across the studied groups, while up to 8.6 % of them had abnormal CSF biomarkers. In 40.3-52.9 % of patients with AD dementia, a typical CSF profile for AD was detected. Approximately 40 % of the potential biomarker constellations are not considered in the NIA-AA guidelines, and more than 40 % of participants could not be classified into the NIA-AA categories with distinct biomarker constellations. Here, a refined scheme covering all potential biomarker constellations is proposed. These results enrich the discussion on the NIA-AA guidelines and point to a discordance between clinical symptomatology and CSF biomarkers even in patients with full-blown AD dementia, who are supposed to have a clearly positive for AD neurochemical profile.
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