TY - JOUR
T1 - Stability of Progranulin Under Pre-Analytical Conditions in Serum and Cerebrospinal Fluid
AU - Willemse, Eline A. J.
AU - Durieux-Lu, Sisi
AU - van der Flier, Wiesje M.
AU - Pijnenburg, Yolande A. L.
AU - de Jonge, Robert
AU - Teunissen, Charlotte E.
PY - 2016
Y1 - 2016
N2 - Progranulin (PGRN) levels in blood and cerebrospinal fluid (CSF) are increasingly studied as potential markers for neurodegenerative disorders. We aimed to 1) characterize two commercially available PGRN ELISAs on several assay validation parameters, 2) assess the stability of PGRN in serum and CSF under pre-analytical conditions, and 3) compare stability in the two assays. Intra-and inter-assay variation, inter-lot variation, linearity, lower limit of detection, and kit correlations were assessed for the Adipogen and R&D PGRN ELISA kits. Blood and serum samples were experimentally exposed to <= 9 freeze/thaw cycles, delayed processing for <= 24 h at room temperature and 4 degrees C, and to temperature stability tests for <= 3 weeks at -20 degrees C, 4 degrees C, room temperature, and 37 degrees C. Both commercial PGRN ELISA kits showed acceptable ranges for intra-and inter-assay variation, where the R&D kit performed more accurate than the Adipogen kit, especially for inter-assay variation (intra-assay serum: 6.7 and 8.3%, respectively; inter-assay serum: 9.2 and 21.0%; intra-assay CSF: 3.6 and 12.0%; inter-assay CSF: 16.0 and 44.5%). Absolute serum PGRN concentrations were 1.9-fold higher in Adipogen than R&D (p <0.001) and strongly correlated between both kits (rho = 0.86, p <0.0001) and CSF PGRN levels were on the borderline of detection in both kits. PGRN was typically stable under all pre-analytical conditions addressed, although two weeks at 37 degrees C resulted in decreased PGRN concentrations in CSF, only when using the Adipogen kit. These results support further examination of PGRN as a potential marker in neurodegenerative diseases, since PGRN is stable in serum and CSF and can be measured using ELISA kits from several providers
AB - Progranulin (PGRN) levels in blood and cerebrospinal fluid (CSF) are increasingly studied as potential markers for neurodegenerative disorders. We aimed to 1) characterize two commercially available PGRN ELISAs on several assay validation parameters, 2) assess the stability of PGRN in serum and CSF under pre-analytical conditions, and 3) compare stability in the two assays. Intra-and inter-assay variation, inter-lot variation, linearity, lower limit of detection, and kit correlations were assessed for the Adipogen and R&D PGRN ELISA kits. Blood and serum samples were experimentally exposed to <= 9 freeze/thaw cycles, delayed processing for <= 24 h at room temperature and 4 degrees C, and to temperature stability tests for <= 3 weeks at -20 degrees C, 4 degrees C, room temperature, and 37 degrees C. Both commercial PGRN ELISA kits showed acceptable ranges for intra-and inter-assay variation, where the R&D kit performed more accurate than the Adipogen kit, especially for inter-assay variation (intra-assay serum: 6.7 and 8.3%, respectively; inter-assay serum: 9.2 and 21.0%; intra-assay CSF: 3.6 and 12.0%; inter-assay CSF: 16.0 and 44.5%). Absolute serum PGRN concentrations were 1.9-fold higher in Adipogen than R&D (p <0.001) and strongly correlated between both kits (rho = 0.86, p <0.0001) and CSF PGRN levels were on the borderline of detection in both kits. PGRN was typically stable under all pre-analytical conditions addressed, although two weeks at 37 degrees C resulted in decreased PGRN concentrations in CSF, only when using the Adipogen kit. These results support further examination of PGRN as a potential marker in neurodegenerative diseases, since PGRN is stable in serum and CSF and can be measured using ELISA kits from several providers
KW - Cerebrospinal fluid
KW - ELISA
KW - human progranulin protein
KW - method comparison
KW - pre-analytical variation
KW - protein stability
KW - serum
U2 - https://doi.org/10.3233/JAD-160061
DO - https://doi.org/10.3233/JAD-160061
M3 - Article
C2 - 27104901
SN - 1387-2877
VL - 53
SP - 107
EP - 116
JO - Journal of Alzheimer s disease
JF - Journal of Alzheimer s disease
IS - 1
ER -