A method for reproducible measurements of serum BDNF: comparison of the performance of six commercial assays

被引:199
作者
Polacchini, Alessio [1 ]
Metelli, Giuliana [1 ]
Francavilla, Ruggiero [1 ]
Baj, Gabriele [1 ]
Florean, Marina [2 ]
Mascaretti, Luca Giovanni [2 ]
Tongiorgi, Enrico [1 ]
机构
[1] Univ Trieste, Dept Life Sci, I-34127 Trieste, Italy
[2] Trieste Univ Hosp, Dept Transfus Med, I-34142 Trieste, Italy
关键词
NEUROTROPHIC FACTOR BDNF; VAL66MET POLYMORPHISM; DIURNAL-VARIATION; CLINICAL UTILITY; BRAIN; DEPRESSION; AGE; HYPOTHESIS; PLATELETS; DISORDER;
D O I
10.1038/srep17989
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Brain-Derived Neurotrophic Factor (BDNF) has attracted increasing interest as potential biomarker to support the diagnosis or monitor the efficacy of therapies in brain disorders. Circulating BDNF can be measured in serum, plasma or whole blood. However, the use of BDNF as biomarker is limited by the poor reproducibility of results, likely due to the variety of methods used for sample collection and BDNF analysis. To overcome these limitations, using sera from 40 healthy adults, we compared the performance of five ELISA kits (Aviscera-Bioscience, Biosensis, Millipore-ChemiKine (TM), PromegaEmax (R), R &) and one multiplexing assay (Millipore-Milliplex (R)). All kits showed 100% sample recovery and comparable range. However, they exhibited very different inter-assay variations from 5% to 20%. Inter-assay variations were higher than those declared by the manufacturers with only one exception which also had the best overall performance. Dot-blot analysis revealed that two kits selectively recognize mature BDNF, while the others reacted with both pro-BDNF and mature BDNF. In conclusion, we identified two assays to obtain reliable measurements of human serum BDNF, suitable for future clinical applications.
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页数:10
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