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Title

Pre-analytical stability of novel cerebrospinal fluid biomarkers

AuthorsWillemse, Eline A. J.; Vermeiren, Yannick; García-Ayllón, María-Salud; Bridel, Claire; Deyn, Peter P. de; Engelborghs, Sebastiaan; Flier, Wiesje M. van der; Jansen, Erwin E. W.; López-Font, Inmaculada; Mendes, Vera; Manadas, Bruno; Roeck, Naomi de; Sáez-Valero, Javier; Struys, Eduard A.; Vanmechelen, Eugeen; Andreasson, Ulf; Teunissen, Charlotte E.
Issue Date2019
PublisherElsevier
CitationClinica Chimica Acta 497: 204-211 (2019)
AbstractStability of the cerebrospinal fluid (CSF) composition under different pre-analytical conditions is relevant for the diagnostic potential of biomarkers. Our aim was to examine the pre-analytical stability of promising CSF biomarkers that are currently evaluated for their discriminative use in various neurological diseases. Pooled CSF was aliquoted and experimentally exposed to delayed storage: 0, 1, 2, 4, 24, 72, or 168 h at 4 °C or room temperature (RT), or 1–4 months at −20 °C; or up to 7 freeze/thaw (f/t) cycles, before final storage at −80 °C. Eleven CSF biomarkers were screened using immunoassays, liquid chromatography, or enzymatic methods. Levels of neurogranin (truncP75), chitinase-3-like protein (YKL-40), beta-site amyloid precursor protein cleaving enzyme 1 (BACE1), acetylcholinesterase (AChE) enzymatic activity, theobromine, secreted protein acidic and rich in cysteine-like 1 (SPARCL-1) and homovanillic acid (HVA) levels were not affected by the applied storage conditions. 3-Methoxy-4-hydroxyphenylglycol (MHPG) levels linearly and strongly decreased after 4 h at RT (−10%) or 24 h at 4 °C (−27%), and with 6% after every f/t cycle. 5-Methyltetrahydrofolate (5-MTHF) (−29% after 1 week at RT) and 5-hydroxyindoleacetic acid levels (5-HIAA) (−16% after 1 week at RT) were reduced and 3,4-dihydroxyphenylacetic acid (DOPAC) levels (+22% after 1 week at RT) increased, but only after >24 h at RT. Ten out of eleven potential CSF novel biomarkers showed very limited change under common storage and f/t conditions, suggesting that these CSF biomarkers can be trustfully tested under the pre-analytical conditions present across different cohorts.
Publisher version (URL)https://doi.org/10.1016/j.cca.2019.07.024
URIhttp://hdl.handle.net/10261/217939
DOIhttp://dx.doi.org/10.1016/j.cca.2019.07.024
ISSN0009-8981
Appears in Collections:(IN) Artículos
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