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The impact of pre-analytical variables on the stability of neurofilament proteins in CSF, determined by a novel validated SinglePlex Luminex assay and ELISA.
Koel-Simmelink, Marleen J A; Vennegoor, Anke; Killestein, Joep; Blankenstein, Marinus A; Norgren, Niklas; Korth, Carsten; Teunissen, Charlotte E.
Afiliação
  • Koel-Simmelink MJ; Department of Clinical Chemistry, VU University Medical Center Amsterdam, PO Box 7057, 1007MB Amsterdam, The Netherlands. Electronic address: mja.koel-simmelink@vumc.nl.
  • Vennegoor A; Department of Neurology, VU University Medical Center Amsterdam, PO Box 7057, 1007MB Amsterdam. The Netherlands. Electronic address: a.vennegoor@vumc.nl.
  • Killestein J; Department of Neurology, VU University Medical Center Amsterdam, PO Box 7057, 1007MB Amsterdam. The Netherlands. Electronic address: j.killestein@vumc.nl.
  • Blankenstein MA; Department of Clinical Chemistry, VU University Medical Center Amsterdam, PO Box 7057, 1007MB Amsterdam, The Netherlands. Electronic address: ma.blankenstein@vumc.nl.
  • Norgren N; UmanDiagnostics, PO Box 7996, 90719 Umeå, Sweden. Electronic address: niklas.norgren@umandiagnostics.se.
  • Korth C; Neurodegeneration Unit, Department Neuropathology, University of Düsseldorf Medical School, Moorenstrase 5, 40225 Düsseldorf, Germany. Electronic address: ckorth@uni-duesseldorf.de.
  • Teunissen CE; Department of Clinical Chemistry, VU University Medical Center Amsterdam, PO Box 7057, 1007MB Amsterdam, The Netherlands. Electronic address: c.teunissen@vumc.nl.
J Immunol Methods ; 402(1-2): 43-9, 2014 Jan 15.
Article em En | MEDLINE | ID: mdl-24275679
ABSTRACT

BACKGROUND:

Neurofilament (Nf) proteins have been shown to be promising biomarkers for monitoring and predicting disease progression for various neurological diseases. The aim of this study was to evaluate the effects of pre-analytical variables on the concentration of neurofilament heavy (NfH) and neurofilament light (NfL) proteins.

METHODS:

For NfH an in-house newly-developed and validated SinglePlex Luminex assay was used; ELISA was used to analyze NfL.

RESULTS:

For the NfL ELISA assay, the intra- and inter-assay variation was respectively, 1.5% and 16.7%. Analytical performance of the NfH SinglePlex Luminex assay in terms of sensitivity (6.6pg/mL), recovery in cerebrospinal fluid (CSF) (between 90 and 104%), linearity (from 6.6-1250pg/mL), and inter- and intra-assay variation (<8%) were good. Concentrations of both NfL and NfH appeared not negatively affected by blood contamination, repeated freeze-thaw cycles (up to 4), delayed processing (up to 24hours) and during long-term storage at -20°C, 4°C, and room temperature. A decrease in concentration was observed during storage of both neurofilament proteins up to 21days at 37°C, which was significant by day 5.

CONCLUSIONS:

The newly developed NfH SinglePlex Luminex assay has a good sensitivity and is robust. Moreover, both NfH and NfL are stable under the most prevalent pre-analytical variations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaio de Imunoadsorção Enzimática / Proteínas de Neurofilamentos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Immunol Methods Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaio de Imunoadsorção Enzimática / Proteínas de Neurofilamentos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Immunol Methods Ano de publicação: 2014 Tipo de documento: Article