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dc.contributor.authorLucey, Brendan P
dc.contributor.authorGonzales, Celedon
dc.contributor.authorDas, Ujjwas
dc.contributor.authorLi, Jinhe
dc.contributor.authorSiemers, Eric R
dc.contributor.authorSlemmon, J. R
dc.contributor.authorBateman, Randall J
dc.contributor.authorHuang, Yafei
dc.contributor.authorFox, Gerard B
dc.contributor.authorClaassen, Jurgen A
dc.contributor.authorSlats, Diane
dc.contributor.authorVerbeek, Marcel M
dc.contributor.authorTong, Gary
dc.contributor.authorSoares, Holly
dc.contributor.authorSavage, Mary J
dc.contributor.authorKennedy, Matthew
dc.contributor.authorForman, Mark
dc.contributor.authorSjögren, Magnus
dc.contributor.authorMargolin, Richard
dc.contributor.authorChen, Xia
dc.contributor.authorFarlow, Martin R
dc.contributor.authorDean, Robert A
dc.contributor.authorWaring, Jeffrey F
dc.date.accessioned2015-09-01T17:44:06Z
dc.date.available2015-09-01T17:44:06Z
dc.date.issued2015-07-29
dc.identifier.citationAlzheimer's Research & Therapy. 2015 Jul 29;7(1):53
dc.identifier.urihttp://dx.doi.org/10.1186/s13195-015-0136-z
dc.identifier.urihttp://hdl.handle.net/10724/31859
dc.description.abstractAbstract 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.
dc.titleAn integrated multi-study analysis of intra-subject variability in cerebrospinal fluid amyloid-β concentrations collected by lumbar puncture and indwelling lumbar catheter
dc.typeJournal Article
dc.date.updated2015-07-29T18:45:08Z
dc.language.rfc3066en
dc.rights.holderLucey et al.


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