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Concordance of cerebrospinal fluid real-time quaking-induced conversion across the European Creutzfeldt-Jakob Disease Surveillance Network.
McKenzie, Neil; Piconi, Gabriele; Culeux, Audrey; Hammarin, Anna-Lena; Stergiou, Christos; Tzartos, Socrates; Versleijen, Alexandra A M; van de Geer, Jacqueline; Cras, Patrick; Cardone, Franco; Ladogana, Anna; Mannana, Angela; Rossi, Marcello; Bongianni, Matilde; Perra, Daniela; Regelsberger, Guenther; Klotz, Sigrid; Hornemann, Simone; Aguzzi, Adriano; Schmitz, Matthias; Andrews, Mary; Burns, Kimberley; Haïk, Stéphane; Ruiz-García, Raquel; Verner-Carlsson, Jenny; Tzartos, John; Verbeek, Marcel M; De Vil, Bart; Poleggi, Anna; Parchi, Piero; Zanusso, Gianluigi; Gelpi, Ellen; Frontzek, Karl; Reimann, Regina; Hermann, Peter; Zerr, Inga; Pal, Suvankar; Green, Alison.
Afiliação
  • McKenzie N; National CJD Research and Surveillance Unit, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Piconi G; National CJD Research and Surveillance Unit, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Culeux A; Sorbonne Université, Institut du Cerveau-Paris Brain Institute, ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.
  • Hammarin AL; Public Health Agency of Sweden, Solna, Sweden.
  • Stergiou C; Tzartos NeuroDiagnostics, Athens, Greece.
  • Tzartos S; Tzartos NeuroDiagnostics, Athens, Greece.
  • Versleijen AAM; Neurochemistry Laboratory-Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • van de Geer J; Neurochemistry Laboratory-Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Cras P; Laboratory of Neurology, University of Antwerp, Antwerp, Belgium.
  • Cardone F; Department of Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
  • Ladogana A; Department of Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
  • Mannana A; Laboratory of Neuropathology, IRCCS Istituto delle Scienze Neurologiche, Bologna, Italy.
  • Rossi M; Laboratory of Neuropathology, IRCCS Istituto delle Scienze Neurologiche, Bologna, Italy.
  • Bongianni M; Neuropathology Laboratory, University of Verona, Verona, Italy.
  • Perra D; Neuropathology Laboratory, University of Verona, Verona, Italy.
  • Regelsberger G; Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Klotz S; Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Hornemann S; Institute of Neuropathology, University Hospital of Zurich, Zürich, Switzerland.
  • Aguzzi A; Institute of Neuropathology, University Hospital of Zurich, Zürich, Switzerland.
  • Schmitz M; National Reference Center for Transmissible Spongiform Encephalopathies, Göttingen, Germany.
  • Andrews M; National CJD Research and Surveillance Unit, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Burns K; National CJD Research and Surveillance Unit, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Haïk S; Sorbonne Université, Institut du Cerveau-Paris Brain Institute, ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.
  • Ruiz-García R; Immunology Department, Biomedical Diagnostic Centre, Hospital Clinic de Barcelona, Barcelona, Spain.
  • Verner-Carlsson J; Neuroimmunology Program, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
  • Tzartos J; Public Health Agency of Sweden, Solna, Sweden.
  • Verbeek MM; Tzartos NeuroDiagnostics, Athens, Greece.
  • De Vil B; Neurochemistry Laboratory-Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Poleggi A; Laboratory of Neurology, University of Antwerp, Antwerp, Belgium.
  • Parchi P; Department of Neuroscience, Istituto Superiore di Sanità, Rome, Italy.
  • Zanusso G; Laboratory of Neuropathology, IRCCS Istituto delle Scienze Neurologiche, Bologna, Italy.
  • Gelpi E; Department of Experimental, Diagnostic, and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
  • Frontzek K; Neuropathology Laboratory, University of Verona, Verona, Italy.
  • Reimann R; Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Hermann P; Institute of Neuropathology, University Hospital of Zurich, Zürich, Switzerland.
  • Zerr I; Institute of Neuropathology, University Hospital of Zurich, Zürich, Switzerland.
  • Pal S; National Reference Center for Transmissible Spongiform Encephalopathies, Göttingen, Germany.
  • Green A; National Reference Center for Transmissible Spongiform Encephalopathies, Göttingen, Germany.
Eur J Neurol ; 29(8): 2431-2438, 2022 08.
Article em En | MEDLINE | ID: mdl-35524506
ABSTRACT
BACKGROUND AND

PURPOSE:

Cerebrospinal fluid (CSF) real-time quaking-induced conversion (RT-QuIC) has a high degree of sensitivity and specificity for the diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD) and this has led to its being included in revised European CJD Surveillance Network diagnostic criteria for sCJD. As CSF RT-QuIC becomes more widely established, it is crucial that the analytical performance of individual laboratories is consistent. The aim of this ring-trial was to ascertain the degree of concordance between European countries undertaking CSF RT-QuIC.

METHODS:

Ten identical CSF samples, seven from probable or neuropathologically confirmed sCJD and three from non-CJD cases, were sent to 13 laboratories from 11 countries for RT-QuIC analysis. A range of instrumentation and different recombinant prion protein substrates were used. Each laboratory analysed the CSF samples blinded to the diagnosis and reported the results as positive or negative.

RESULTS:

All 13 laboratories correctly identified five of the seven sCJD cases and the remaining two sCJD cases were identified by 92% of laboratories. Of the two sCJD cases that were not identified by all laboratories, one had a disease duration >26 months with a negative 14-3-3, whilst the remaining case had a 4-month disease duration and a positive 14-3-3. A single false positive CSF RT-QuIC result was observed in this study.

CONCLUSIONS:

This study shows that CSF RT-QuIC demonstrates an excellent concordance between centres, even when using a variety of instrumentation, recombinant prion protein substrates and CSF volumes. The adoption of CSF RT-QuIC by all CJD surveillance centres is recommended.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Príons / Síndrome de Creutzfeldt-Jakob Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Príons / Síndrome de Creutzfeldt-Jakob Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Eur J Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido