Evidence map›Paper›PMID 29143217›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2018

Fluid biomarker agreement and interrelation in dementia due to Alzheimer's disease.

Panagiotis Alexopoulos, Jennifer Roesler, Lukas Werle, Nathalie Thierjung, Iliana Lentzari, Marion Ortner, Timo Grimmer, Nikolaos Laskaris, Antonios Politis, Philippos Gourzis and 3 more

Abstract read
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In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 7 institutions in 4 countries.

Panagiotis AlexopoulosDepartment of Psychiatry, University of Patras, 26500, Rion Patras, Greece. panos.alexopoulos@upatras.gr.ORCID 0000-0002-9047-6365
Jennifer RoeslerDepartment of Psychiatry and Psychotherapy, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.
Lukas WerleDepartment of Psychiatry and Psychotherapy, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.
Nathalie ThierjungDepartment of Psychiatry and Psychotherapy, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.
Iliana LentzariDepartment of Psychiatry, University of Patras, 26500, Rion Patras, Greece.
Marion OrtnerDepartment of Psychiatry and Psychotherapy, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.
Timo GrimmerDepartment of Psychiatry and Psychotherapy, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.
Nikolaos LaskarisDepartment of Informatics, Aristotle University of Thessaloniki, 54124, Thessaloniki, Greece.
Antonios PolitisFirst Department of Psychiatry, Eginition Hospital, National and Kapodistrian University of Athens, Vassilissis Sofias Ave 72-74, 11528, Athens, Greece.
Philippos GourzisDepartment of Psychiatry, University of Patras, 26500, Rion Patras, Greece.
Alexander KurzDepartment of Psychiatry and Psychotherapy, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.
Robert PerneczkyDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilians-Universität München, Nussbaumstraße 7, 80336, Munich, Germany.
Alzheimer’s Disease Neuroimaging Initiative
University of Patras · GRTechnical University of Munich · DEAristotle University of Thessaloniki · GRGerman Center for Neurodegenerative Diseases · DEJohns Hopkins University · USMax Planck Institute of Psychiatry · DENational and Kapodistrian University of Athens · GR

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
NIA NIH HHS U01 AG024904
6 · The paper itself

Abstract

The cerebrospinal fluid (CSF) levels of β-amyloid 42, total tau, and phosphorylated tau 181 are supposed to be all continuously abnormal in dementia due to Alzheimer's disease (AD), being the most advanced disease stage. The aim of the present study, which included a monocentric and a multicentric sample (N = 119 and 178, respectively), was to investigate the degree of CSF biomarker agreement and interrelation in AD dementia. Based on previously published cut-off values, biomarker values were categorized as positive or negative for AD (dichotomization strategy) and as either positive, negative, or borderline (trichotomization strategy). The statistical analyses relied on distance correlation analysis and kappa (k) statistics. Poor agreement (k < 0.4) and low interrelations between the studied biomarkers were detected in all cases with the exception of the interrelation between the markers total tau and phosphorylated tau 181, especially in the monocentric sample. Interestingly, lower interrelation and agreement degrees were observed in carriers of the Apolipoprotein E ε4 allele compared to non-carriers. The clinical phenotype currently referred to as "AD dementia" is characterized by an inhomogeneous CSF biomarker profile, possibly mirroring the complex genesis of AD-typical dementia symptoms and pointing to the necessity of shedding more light on the hypothesis of biomarker stability over time in symptomatic AD.

Indexed as

AgedAged, 80 and overAlzheimer DiseaseAmyloid beta-PeptidesBiomarkersDementiaFemaleHumansMaleMiddle Agedtau ProteinsAmyloid beta-PeptidesBiomarkerstau ProteinsPhosphorylated tau 181Total tauβ-Amyloid 1-42

Identifiers

PMID29143217
OpenAlexW2770162443

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.