Cerebrospinal fluid tau and Aβ42 concentrations in healthy subjects: delineation of reference intervals and their limitations
Gespeichert in:
Verfasser / Beitragende:
[Pierre R. Burkhard, Roxane Fournier, Bernadette Mermillod, Karl-Heinz Krause, Constantin Bouras, Irmgard Irminger]
Ort, Verlag, Jahr:
2004
Enthalten in:
Clinical Chemistry and Laboratory Medicine, 42/4(2004-04-05), 396-407
Format:
Artikel (online)
Online Zugang:
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| 024 | 7 | 0 | |a 10.1515/CCLM.2004.071 |2 doi |
| 035 | |a (NATIONALLICENCE)gruyter-10.1515/CCLM.2004.071 | ||
| 245 | 0 | 0 | |a Cerebrospinal fluid tau and Aβ42 concentrations in healthy subjects: delineation of reference intervals and their limitations |h [Elektronische Daten] |c [Pierre R. Burkhard, Roxane Fournier, Bernadette Mermillod, Karl-Heinz Krause, Constantin Bouras, Irmgard Irminger] |
| 520 | 3 | |a Many limitations and conflicting results have cast serious doubts on the validity of cerebrospinal fluid tau and Aβ42 levels for the biological diagnosis of Alzheimer's disease, particularly extreme variations of the reference limits found by unrelated groups as a consequence of different reference populations used. In this study, we addressed the issue of defining reference limits for cerebrospinal fluid tau and Aβ42 in healthy adult individuals. One hundred and five neurologically intact subjects were enrolled according to strict inclusion criteria, 10 of them with autopsy confirmation of brain integrity. All cerebrospinal fluid samples were similarly and optimally processed as were the dosage methods used and the statistical analyses performed. A robust correlation with age was demonstrated for Aβ42 but not for tau. For tau, we found that an upper cut-off value of 443 ng/l allowed 95% of the subjects to be correctly classified as normal. For Aβ42, a lower cut-off value of 90 ng/l allowed a correct classification of 90% of the subjects. However, a large variance of the reference values, partly explained by the potential contamination of the reference population with presymptomatic dementia patients, may limit the use of reference limits based on living subjects. We propose that the issue of defining reference limits for both cerebrospinal fluid tau and Aβ42 may ultimately be settled by studying large numbers of autopsy-proven neurologically intact individuals only. | |
| 540 | |a Copyright © 2004 by Walter de Gruyter GmbH & Co. KG | ||
| 690 | 7 | |a Medical equipment & techniques |2 nationallicence | |
| 690 | 7 | |a Medical diagnosis |2 nationallicence | |
| 690 | 7 | |a Diseases & disorders |2 nationallicence | |
| 700 | 1 | |a Burkhard |D Pierre R. |4 aut | |
| 700 | 1 | |a Fournier |D Roxane |4 aut | |
| 700 | 1 | |a Mermillod |D Bernadette |4 aut | |
| 700 | 1 | |a Krause |D Karl-Heinz |4 aut | |
| 700 | 1 | |a Bouras |D Constantin |4 aut | |
| 700 | 1 | |a Irminger |D Irmgard |4 aut | |
| 773 | 0 | |t Clinical Chemistry and Laboratory Medicine |d Walter de Gruyter |g 42/4(2004-04-05), 396-407 |x 1434-6621 |q 42:4<396 |1 2004 |2 42 |o cclm | |
| 856 | 4 | 0 | |u https://doi.org/10.1515/CCLM.2004.071 |q text/html |z Onlinezugriff via DOI |
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| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1515/CCLM.2004.071 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Burkhard |D Pierre R. |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Fournier |D Roxane |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Mermillod |D Bernadette |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Krause |D Karl-Heinz |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Bouras |D Constantin |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Irminger |D Irmgard |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Clinical Chemistry and Laboratory Medicine |d Walter de Gruyter |g 42/4(2004-04-05), 396-407 |x 1434-6621 |q 42:4<396 |1 2004 |2 42 |o cclm | ||
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