001     282304
005     20251117142809.0
024 7 _ |a 10.1007/s00406-023-01751-2
|2 doi
024 7 _ |a pmid:38316685
|2 pmid
024 7 _ |a 1433-8491
|2 ISSN
024 7 _ |a 0003-9373
|2 ISSN
037 _ _ |a DZNE-2025-01274
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Marcos Morgado, Barbara
|0 P:(DE-2719)9003591
|b 0
|u dzne
245 _ _ |a Assessment of immunoprecipitation with subsequent immunoassays for the blood-based diagnosis of Alzheimer's disease.
260 _ _ |a Heidelberg
|c 2024
|b Springer
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1763385981_17166
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
500 _ _ |a ISSN 1433-8491 not unique: **2 hits**.
520 _ _ |a The Aβ42/40 ratio and the concentration of phosphorylated Tau181 in blood plasma represent attractive biomarkers for Alzheimer's disease. As a means for reducing potential matrix effects, which may interfere with plasma immunoassays, we have previously developed a pre-analytical sample workup by semi-automated immunoprecipitation. Here we test the compatibility of pre-analytical immunoprecipitations with automated Aβ1-40, Aβ1-42 and phosphorylated Tau181 immunoassays on the Lumipulse platform and compare the diagnostic performance of the respective immunoprecipitation immunoassay approaches with direct plasma measurements. 71 participants were dichotomized according to their Aβ42/40 ratios in cerebrospinal fluid into the diagnostic groups amyloid-positive (n = 32) and amyloid-negative (n = 39). The plasma Aβ1-42/1-40 ratio and phosphorylated Tau181 levels were determined on the Lumipulse G600II platform (Fujirebio) by direct measurements in EDTA-plasma or after Aβ- or Tau-immunoprecipitation, respectively. Pre-analytical immunoprecipitation of Aβ turned out to be compatible with the Lumipulse Aβ assays and resulted in a numerical, yet statistically not significant increase in the area under the ROC curve for plasma Aβ1-42/1-40. Additionally, we observed a significant increase in the standardised effect size (Cohen's D). Pre-analytical immunoprecipitation of Tau resulted in increased differences between the diagnostic groups in terms of median and mean phosphorylated Tau 181 levels. Furthermore, we observed a greater Cohen's d (p < 0.001) and a larger area under the ROC curve (p = 0.038) after Tau-IP. Our preliminary findings in a small, preselected sample indicate that pre-analytical immunoprecipitation may have the potential to improve the diagnostic performance of plasma biomarker immunoassays for Aβ1-42/1-40 and phosphorylated Tau181 to predict brain amyloid deposition.
536 _ _ |a 353 - Clinical and Health Care Research (POF4-353)
|0 G:(DE-HGF)POF4-353
|c POF4-353
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: pub.dzne.de
650 _ 7 |a Alzheimer’s disease
|2 Other
650 _ 7 |a Amyloid beta
|2 Other
650 _ 7 |a Biomarker
|2 Other
650 _ 7 |a Blood plasma
|2 Other
650 _ 7 |a Tau
|2 Other
700 1 _ |a Klafki, Hans-Wolfgang
|0 0000-0002-8672-9032
|b 1
700 1 _ |a Bauer, Chris
|0 0000-0002-4199-5468
|b 2
700 1 _ |a Waniek, Katharina
|0 0000-0002-2925-5790
|b 3
700 1 _ |a Esselmann, Hermann
|0 0000-0001-5484-9710
|b 4
700 1 _ |a Wirths, Oliver
|0 0000-0002-4115-0334
|b 5
700 1 _ |a Hansen, Niels
|0 0000-0001-5785-9594
|b 6
700 1 _ |a Lachmann, Ingolf
|0 0000-0002-9225-1493
|b 7
700 1 _ |a Osterloh, Dirk
|0 0009-0002-8832-3164
|b 8
700 1 _ |a Schuchhardt, Johannes
|0 0009-0008-8896-4328
|b 9
700 1 _ |a Wiltfang, Jens
|0 P:(DE-2719)2811317
|b 10
773 _ _ |a 10.1007/s00406-023-01751-2
|0 PERI:(DE-600)2793981-9
|p -
|t Archiv für Psychiatrie und Nervenkrankheiten
|v Advance online publication
|y 2024
|x 1433-8491
910 1 _ |a External Institute
|0 I:(DE-HGF)0
|k Extern
|b 0
|6 P:(DE-2719)9003591
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 10
|6 P:(DE-2719)2811317
913 1 _ |a DE-HGF
|b Gesundheit
|l Neurodegenerative Diseases
|1 G:(DE-HGF)POF4-350
|0 G:(DE-HGF)POF4-353
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Clinical and Health Care Research
|x 0
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2024-12-05
920 1 _ |0 I:(DE-2719)1410006
|k AG Wiltfang
|l Molecular biomarkers for predictive diagnostics of neurodegenerative diseases
|x 0
980 _ _ |a journal
980 _ _ |a EDITORS
980 _ _ |a VDBINPRINT
980 _ _ |a I:(DE-2719)1410006
980 _ _ |a UNRESTRICTED


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