کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1966070 | 1538693 | 2012 | 8 صفحه PDF | دانلود رایگان |
BackgroundAlthough important improvements of downstream molecular in vitro diagnostics assays based on RNA from blood were made, the pre-analytical workflow is still poorly defined.MethodsWe performed a multicenter study within the EU-granted SPIDIA project to investigate blood collection and shipping influence on the following RNA quality parameters: yield, purity, integrity, RT-qPCR interference and IL1B, IL8, FOS and GAPDH gene expression. Two models were designed: Exp A. Ten laboratories collected blood from an own donor into two different tubes (with or without stabilizer) and extracted RNA at two different times; Exp B. Blood was drawn from a single donor and shipped to ten laboratories in two different tubes (with or without stabilizer) for RNA extraction.ResultsIn both models and collection tubes, reliable results were obtained for purity, yield, GAPDH expression, and interferences. A substantial variation in RIN (Exp A) and in transcription levels of IL1B, IL8 and FOS (Exp B) was observed for blood collected in tube without stabilizer tubes. Overall the variability was higher among data obtained from unstabilized blood samples.ConclusionsWe defined the experimental setup for a larger ring trial throughout Europe. The chosen downstream analyses verified their potential, serving as adequate markers to test the quality of blood RNA.
► Multicenter pilot study for Proficiency Testing to develop a Pan-European ring trial.
► PT is based on pre-analytical phase of RNA extraction from blood.
► Evaluation of blood collection and blood and RNA shipping.
► Setup of a panel of parameters to test quality of blood RNA.
Journal: Clinica Chimica Acta - Volume 413, Issues 7–8, 11 April 2012, Pages 779–786