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Neurochemical Dementia Diagnostics - Interlaboratory Variation of Analysis, Reference Ranges and Interpretations | OMICS International | Abstract
ISSN: 2161-0460

Journal of Alzheimers Disease & Parkinsonism
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Research Article

Neurochemical Dementia Diagnostics - Interlaboratory Variation of Analysis, Reference Ranges and Interpretations

Hansotto Reiber1*, Peter Lange2 and Inga Zerr2

1 Soc. for Advancement of Quality Assurance in Medical Laboratories, INSTAND, Düsseldorf, Germany

2 Neurochemistry Laboratory, Department of Neurology, University Medical Center, Georg August University Göttingen, Germany

Corresponding Author:
Hansotto Reiber
Soc. for Advancement of Quality Assurance in Medical Laboratories
INSTAND, Düsseldorf, Germany
Tel: 005511982787549
E-mail: [email protected]

Received date: March 20, 2014; Accepted date: April 22, 2014; Published date: May 20, 2014

Citation: Reiber H, Lange P, Zerr I (2014) Neurochemical Dementia Diagnostics – Interlaboratory Variation of Analysis, Reference Ranges and Interpretations. J Alzheimers Dis Parkinsonism 4:147. doi: 10.4172/2161-0460.1000147

Copyright: © 2014 Reiber H, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


Purpose: Dementia marker analysis requests the control of analytical reliability. Method: 49 laboratories from nine European countries and USA participate in the first external quality assessment system [EQAS] for dementia marker analysis. Stabilized CSF samples are analyzed with a reference range-related evaluation and a differential diagnostic interpretation of combined parameters [total Tau protein, phospho Tau protein and Amyloid-ß-peptide Aß1-42]. Results: A) The large inter-laboratory variation is characterized by a survey-example with values in the decision range: the highest value was 10-fold higher than the lowest for Aß42 [69-771 pg/ml], 4-fold higher for Tau [315-1292 pg/ml and twofold for pTau[53-83 pg/ml]. With a success range of median ± 25% the fraction of outliers were up to 31% [Aß42] or 13-15% [Tau] and 3-11% for pTau in the N= 6 surveys. B) For evaluation [normal /pathological/border line] participants used a huge range of individual cut-off values: Tau [150-540, median 450 pg/ml], pTau [35-85, median 61 pg/ml] and Aß1-42 [205-600, median 500 pg/ml] with serious consequences for the differential diagnosis. C) In case of a sample with normal median values [e.g. Tau = 381 pg/ml and Aß= 748 pg/ml] 45% of participants regarded their values as pathological with a stunning interpretation of combined Tau and Aß1-42 data: 29% of the participants found this data combination compatible with an Alzheimer’s disease, 29% reported this as a normal sample, and 42 % regarded an interpretation as not possible. Conclusions: Up to 31% outliers are a source of serious diagnostic errors. The unacceptable large variation of the laboratory own cut-off values leads to false negative and false positive diagnostic interpretations. This questions the practical relevance of dementia marker analysis. The calculation of mathematical formulas or ratios is not improving the discriminative sensitivity due to the error propagation in mathematical functions.


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