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Diagnosis of Human Prion Disease Using Real-Time Quaking-Induced Conversion Testing of Olfactory Mucosa and Cerebrospinal Fluid Samples.
Bongianni, Matilde; Orrù, Christina; Groveman, Bradley R; Sacchetto, Luca; Fiorini, Michele; Tonoli, Giovanni; Triva, Giorgio; Capaldi, Stefano; Testi, Silvia; Ferrari, Sergio; Cagnin, Annachiara; Ladogana, Anna; Poleggi, Anna; Colaizzo, Elisa; Tiple, Dorina; Vaianella, Luana; Castriciano, Santina; Marchioni, Daniele; Hughson, Andrew G; Imperiale, Daniele; Cattaruzza, Tatiana; Fabrizi, Gian Maria; Pocchiari, Maurizio; Monaco, Salvatore; Caughey, Byron; Zanusso, Gianluigi.
Afiliação
  • Bongianni M; Department of Neurosciences, Biomedicine, and Movement Sciences, University of Verona, Policlinico G. B. Rossi, Verona, Italy.
  • Orrù C; Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana.
  • Groveman BR; Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana.
  • Sacchetto L; Department of Surgical Sciences, Dentistry, Gynecology, and Pediatrics, University of Verona, Verona, Italy.
  • Fiorini M; Department of Neurosciences, Biomedicine, and Movement Sciences, University of Verona, Policlinico G. B. Rossi, Verona, Italy.
  • Tonoli G; Struttura Complessa di Otorinolaringoiatria, Ospedale Santa Maria della Misericordia, Rovigo, Italy.
  • Triva G; Copan Italia SpA, Brescia, Italy.
  • Capaldi S; Biocrystallography Laboratory, Department of Biotechnology, University of Verona, Italy.
  • Testi S; Department of Neurosciences, Biomedicine, and Movement Sciences, University of Verona, Policlinico G. B. Rossi, Verona, Italy.
  • Ferrari S; Department of Neurosciences, Biomedicine, and Movement Sciences, University of Verona, Policlinico G. B. Rossi, Verona, Italy.
  • Cagnin A; Department of Neuroscience, University of Padova, Padova, Italy8Istituto di Ricovero e Cura a Carattere Scientifico San Camillo Hospital, Venice, Italy.
  • Ladogana A; Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome, Italy.
  • Poleggi A; Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome, Italy.
  • Colaizzo E; Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome, Italy.
  • Tiple D; Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome, Italy.
  • Vaianella L; Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome, Italy.
  • Castriciano S; Copan Italia SpA, Brescia, Italy.
  • Marchioni D; Department of Surgical Sciences, Dentistry, Gynecology, and Pediatrics, University of Verona, Verona, Italy.
  • Hughson AG; Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana.
  • Imperiale D; Neurology Unit, Ospedale Maria Vittoria, Torino, Italy.
  • Cattaruzza T; Neurology Unit, Ospedale Cattinara, Trieste, Italy.
  • Fabrizi GM; Department of Neurosciences, Biomedicine, and Movement Sciences, University of Verona, Policlinico G. B. Rossi, Verona, Italy.
  • Pocchiari M; Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome, Italy.
  • Monaco S; Department of Neurosciences, Biomedicine, and Movement Sciences, University of Verona, Policlinico G. B. Rossi, Verona, Italy.
  • Caughey B; Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana.
  • Zanusso G; Department of Neurosciences, Biomedicine, and Movement Sciences, University of Verona, Policlinico G. B. Rossi, Verona, Italy.
JAMA Neurol ; 74(2): 155-162, 2017 02 01.
Article em En | MEDLINE | ID: mdl-27942718
ABSTRACT
Importance Early and accurate in vivo diagnosis of Creutzfeldt-Jakob disease (CJD) is necessary for quickly distinguishing treatable from untreatable rapidly progressive dementias and for future therapeutic trials. This early diagnosis is becoming possible using the real-time quaking-induced conversion (RT-QuIC) seeding assay, which detects minute amounts of the disease-specific pathologic prion protein in cerebrospinal fluid (CSF) or olfactory mucosa (OM) samples.

Objective:

To develop an algorithm for accurate and early diagnosis of CJD by using the RT-QuIC assay on CSF samples, OM samples, or both. Design, Setting, and

Participants:

In this case-control study, samples of CSF and OM were collected from 86 patients with a clinical diagnosis of probable (n = 51), possible (n = 24), or suspected (n = 11) CJD and 104 negative control samples (54 CSF and 50 OM). The CSF and OM samples were analyzed using conventional RT-QuIC. The CSF samples underwent further testing using improved RT-QuIC conditions. In addition, the diagnostic performance of a novel, easy-to-use, gentle flocked swab for sampling of OM was evaluated. Data were collected from January 1 to June 30, 2015. Main Outcome and

Measures:

Correlations between RT-QuIC results and the final diagnosis of recruited patients.

Results:

Among the 86 patients (37 men [43%] and 49 women [57%]; mean [SD] age, 65.7 [11.5] years) included for analysis, all 61 patients with sporadic CJD had positive RT-QuIC findings using OM or CSF samples or both for an overall RT-QuIC diagnostic sensitivity of 100% (95% CI, 93%-100%). All patients with a final diagnosis of non-prion disease (71 CSF and 67 OM samples) had negative RT-QuIC findings for 100% specificity (95% CI, 94%-100%). Of 8 symptomatic patients with various mutations causing CJD or Gerstmann-Sträussler-Scheinker syndrome, 6 had positive and 2 had negative RT-QuIC findings for a sensitivity of 75% (95% CI, 36%-96%). Conclusions and Relevance A proposed diagnostic algorithm for sporadic CJD combines CSF and OM RT-QuIC testing to provide virtually 100% diagnostic sensitivity and specificity in the clinical phase of the disease.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Príons / Mucosa Olfatória / Síndrome de Creutzfeldt-Jakob Tipo de estudo: Diagnostic_studies / Observational_studies / Screening_studies Limite: Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Príons / Mucosa Olfatória / Síndrome de Creutzfeldt-Jakob Tipo de estudo: Diagnostic_studies / Observational_studies / Screening_studies Limite: Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article