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An integrated multi-study analysis of intra-subject variability in cerebrospinal fluid amyloid-β concentrations collected by lumbar puncture and indwelling lumbar catheter

INTRODUCTION: Amyloid-β (Aβ) has been investigated as a diagnostic biomarker and therapeutic drug target. Recent studies found that cerebrospinal fluid (CSF) Aβ fluctuates over time, including as a diurnal pattern, and increases in absolute concentration with serial collection. It is currently unkno...

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Autores principales: Lucey, Brendan P., Gonzales, Celedon, Das, Ujjwas, Li, Jinhe, Siemers, Eric R., Slemmon, J. Randall, Bateman, Randall J., Huang, Yafei, Fox, Gerard B., Claassen, Jurgen A.H.R., Slats, Diane, Verbeek, Marcel M., Tong, Gary, Soares, Holly, Savage, Mary J., Kennedy, Matthew, Forman, Mark, Sjögren, Magnus, Margolin, Richard, Chen, Xia, Farlow, Martin R., Dean, Robert A., Waring, Jeffrey F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518529/
https://www.ncbi.nlm.nih.gov/pubmed/26225140
http://dx.doi.org/10.1186/s13195-015-0136-z
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author Lucey, Brendan P.
Gonzales, Celedon
Das, Ujjwas
Li, Jinhe
Siemers, Eric R.
Slemmon, J. Randall
Bateman, Randall J.
Huang, Yafei
Fox, Gerard B.
Claassen, Jurgen A.H.R.
Slats, Diane
Verbeek, Marcel M.
Tong, Gary
Soares, Holly
Savage, Mary J.
Kennedy, Matthew
Forman, Mark
Sjögren, Magnus
Margolin, Richard
Chen, Xia
Farlow, Martin R.
Dean, Robert A.
Waring, Jeffrey F.
author_facet Lucey, Brendan P.
Gonzales, Celedon
Das, Ujjwas
Li, Jinhe
Siemers, Eric R.
Slemmon, J. Randall
Bateman, Randall J.
Huang, Yafei
Fox, Gerard B.
Claassen, Jurgen A.H.R.
Slats, Diane
Verbeek, Marcel M.
Tong, Gary
Soares, Holly
Savage, Mary J.
Kennedy, Matthew
Forman, Mark
Sjögren, Magnus
Margolin, Richard
Chen, Xia
Farlow, Martin R.
Dean, Robert A.
Waring, Jeffrey F.
author_sort Lucey, Brendan P.
collection PubMed
description INTRODUCTION: Amyloid-β (Aβ) has been investigated as a diagnostic biomarker and therapeutic drug target. Recent studies found that cerebrospinal fluid (CSF) Aβ fluctuates over time, including as a diurnal pattern, and increases in absolute concentration with serial collection. It is currently unknown what effect differences in CSF collection methodology have on Aβ variability. In this study, we sought to determine the effect of different collection methodologies on the stability of CSF Aβ concentrations over time. METHODS: Grouped analysis of CSF Aβ levels from multiple industry and academic groups collected by either lumbar puncture (n=83) or indwelling lumbar catheter (n=178). Participants were either placebo or untreated subjects from clinical drug trials or observational studies. Participants had CSF collected by lumbar puncture or lumbar catheter for quantitation of Aβ concentration by enzyme linked immunosorbent assay. Data from all sponsors was converted to percent of the mean for Aβ40 and Aβ42 for comparison. Repeated measures analysis of variance was performed to assess for factors affecting the linear rise of Aβ concentrations over time. RESULTS: Analysis of studies collecting CSF via lumbar catheter revealed tremendous inter-subject variability of Aβ40 and Aβ42 as well as an Aβ diurnal pattern in all of the sponsors’ studies. In contrast, Aβ concentrations from CSF samples collected at two time points by lumbar puncture showed no significant differences. Repeated measures analysis of variance found that only time and draw frequency were significantly associated with the slope of linear rise in Aβ40 and Aβ42 concentrations during the first 6 hours of collection. CONCLUSIONS: Based on our findings, we recommend minimizing the frequency of CSF draws in studies measuring Aβ levels and keeping the frequency standardized between experimental groups. The Aβ diurnal pattern was noted in all sponsors’ studies and was not an artifact of study design. Averaging Aβ concentrations at each time point is recommended to minimize the effect of individual variability. Indwelling lumbar catheters are an invaluable research tool for following changes in CSF Aβ over 24-48 hours, but factors affecting Aβ concentration such as linear rise and diurnal variation need to be accounted for in planning study designs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13195-015-0136-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-45185292015-07-30 An integrated multi-study analysis of intra-subject variability in cerebrospinal fluid amyloid-β concentrations collected by lumbar puncture and indwelling lumbar catheter Lucey, Brendan P. Gonzales, Celedon Das, Ujjwas Li, Jinhe Siemers, Eric R. Slemmon, J. Randall Bateman, Randall J. Huang, Yafei Fox, Gerard B. Claassen, Jurgen A.H.R. Slats, Diane Verbeek, Marcel M. Tong, Gary Soares, Holly Savage, Mary J. Kennedy, Matthew Forman, Mark Sjögren, Magnus Margolin, Richard Chen, Xia Farlow, Martin R. Dean, Robert A. Waring, Jeffrey F. Alzheimers Res Ther Research INTRODUCTION: Amyloid-β (Aβ) has been investigated as a diagnostic biomarker and therapeutic drug target. Recent studies found that cerebrospinal fluid (CSF) Aβ fluctuates over time, including as a diurnal pattern, and increases in absolute concentration with serial collection. It is currently unknown what effect differences in CSF collection methodology have on Aβ variability. In this study, we sought to determine the effect of different collection methodologies on the stability of CSF Aβ concentrations over time. METHODS: Grouped analysis of CSF Aβ levels from multiple industry and academic groups collected by either lumbar puncture (n=83) or indwelling lumbar catheter (n=178). Participants were either placebo or untreated subjects from clinical drug trials or observational studies. Participants had CSF collected by lumbar puncture or lumbar catheter for quantitation of Aβ concentration by enzyme linked immunosorbent assay. Data from all sponsors was converted to percent of the mean for Aβ40 and Aβ42 for comparison. Repeated measures analysis of variance was performed to assess for factors affecting the linear rise of Aβ concentrations over time. RESULTS: Analysis of studies collecting CSF via lumbar catheter revealed tremendous inter-subject variability of Aβ40 and Aβ42 as well as an Aβ diurnal pattern in all of the sponsors’ studies. In contrast, Aβ concentrations from CSF samples collected at two time points by lumbar puncture showed no significant differences. Repeated measures analysis of variance found that only time and draw frequency were significantly associated with the slope of linear rise in Aβ40 and Aβ42 concentrations during the first 6 hours of collection. CONCLUSIONS: Based on our findings, we recommend minimizing the frequency of CSF draws in studies measuring Aβ levels and keeping the frequency standardized between experimental groups. The Aβ diurnal pattern was noted in all sponsors’ studies and was not an artifact of study design. Averaging Aβ concentrations at each time point is recommended to minimize the effect of individual variability. Indwelling lumbar catheters are an invaluable research tool for following changes in CSF Aβ over 24-48 hours, but factors affecting Aβ concentration such as linear rise and diurnal variation need to be accounted for in planning study designs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13195-015-0136-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-29 /pmc/articles/PMC4518529/ /pubmed/26225140 http://dx.doi.org/10.1186/s13195-015-0136-z Text en © Lucey et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lucey, Brendan P.
Gonzales, Celedon
Das, Ujjwas
Li, Jinhe
Siemers, Eric R.
Slemmon, J. Randall
Bateman, Randall J.
Huang, Yafei
Fox, Gerard B.
Claassen, Jurgen A.H.R.
Slats, Diane
Verbeek, Marcel M.
Tong, Gary
Soares, Holly
Savage, Mary J.
Kennedy, Matthew
Forman, Mark
Sjögren, Magnus
Margolin, Richard
Chen, Xia
Farlow, Martin R.
Dean, Robert A.
Waring, Jeffrey F.
An integrated multi-study analysis of intra-subject variability in cerebrospinal fluid amyloid-β concentrations collected by lumbar puncture and indwelling lumbar catheter
title An integrated multi-study analysis of intra-subject variability in cerebrospinal fluid amyloid-β concentrations collected by lumbar puncture and indwelling lumbar catheter
title_full An integrated multi-study analysis of intra-subject variability in cerebrospinal fluid amyloid-β concentrations collected by lumbar puncture and indwelling lumbar catheter
title_fullStr An integrated multi-study analysis of intra-subject variability in cerebrospinal fluid amyloid-β concentrations collected by lumbar puncture and indwelling lumbar catheter
title_full_unstemmed An integrated multi-study analysis of intra-subject variability in cerebrospinal fluid amyloid-β concentrations collected by lumbar puncture and indwelling lumbar catheter
title_short An integrated multi-study analysis of intra-subject variability in cerebrospinal fluid amyloid-β concentrations collected by lumbar puncture and indwelling lumbar catheter
title_sort integrated multi-study analysis of intra-subject variability in cerebrospinal fluid amyloid-β concentrations collected by lumbar puncture and indwelling lumbar catheter
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518529/
https://www.ncbi.nlm.nih.gov/pubmed/26225140
http://dx.doi.org/10.1186/s13195-015-0136-z
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