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Superiority of Droplet Digital PCR Over Real-Time Quantitative PCR for JAK2 V617F Allele Mutational Burden Assessment in Myeloproliferative Neoplasms: A Retrospective Study

Authors :
Oreste Villani
Geppino Falco
Anna Marinaccio
Vitalba Ruggieri
Francesco La Rocca
Maria Iole Natalicchio
Vitina Grieco
Simona Laurino
Pellegrino Musto
Pietro Zoppoli
Francesco Albano
Emanuela Zifarone
Giovanni Calice
Sabino Russi
La Rocca, F
Grieco, V
Ruggieri, V
Zifarone, E
Villani, O
Zoppoli, P
Russi, S
Laurino, S
Falco, G
Calice, G
Marinaccio, A
Natalicchio, Mi
Albano, F
Musto, P.
Source :
Diagnostics, Volume 10, Issue 3, Diagnostics, Vol 10, Iss 3, p 143 (2020), Diagnostics (Basel) 10 (2020). doi:10.3390/diagnostics10030143, info:cnr-pdr/source/autori:La Rocca, Francesco; Grieco, Vitina; Ruggieri, Vitalba; Zifarone, Emanuela; Villani, Oreste; Zoppoli, Pietro; Russi, Sabino; Laurino, Simona; Falco, Geppino; Calice, Giovanni; Marinaccio, Anna; Natalicchio, Maria Iole; Albano, Francesco; Musto, Pellegrino/titolo:Superiority of Droplet Digital PCR Over Real-Time Quantitative PCR for JAK2 V617F Allele Mutational Burden Assessment in Myeloproliferative Neoplasms: A Retrospective Study/doi:10.3390%2Fdiagnostics10030143/rivista:Diagnostics (Basel)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:10
Publication Year :
2020
Publisher :
MDPI AG, 2020.

Abstract

JAK2 V617F mutational status is an essential diagnostic index in myeloproliferative neoplasms (MPNs). Although widely used for detection of JAK2 V617F mutation in peripheral blood (PB), sensitive real-time quantitative PCR (qPCR) presents some methodological limitations. Recently, emerging alternative technologies, like digital droplet PCR (ddPCR), have been reported to overcome some of qPCR&rsquo<br />s technical drawbacks. The purpose of this study was to compare the diagnostic utility of ddPCR to qPCR for JAK2 V617F detection and quantification in samples from MPNs patients. Sensitivity and specificity of qPCR and ddPCR in the detection of the mutation were assessed by using a calibrator panel of mutated DNA on 195 JAK2 positive MPN samples. Based on our results, ddPCR proved to be a suitable, precise, and sensitive method for detection and quantification of the JAK2 V617F mutation.

Details

ISSN :
20754418
Volume :
10
Database :
OpenAIRE
Journal :
Diagnostics
Accession number :
edsair.doi.dedup.....252d0157eff5482dffd31ec05ac5887a
Full Text :
https://doi.org/10.3390/diagnostics10030143