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Diagnosis of prion diseases by RT-QuIC results in improved surveillance.
Rhoads, Daniel D; Wrona, Aleksandra; Foutz, Aaron; Blevins, Janis; Glisic, Kathleen; Person, Marissa; Maddox, Ryan A; Belay, Ermias D; Schonberger, Lawrence B; Tatsuoka, Curtis; Cohen, Mark L; Appleby, Brian S.
Afiliación
  • Rhoads DD; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Wrona A; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Foutz A; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Blevins J; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Glisic K; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Person M; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Maddox RA; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Belay ED; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Schonberger LB; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Tatsuoka C; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Cohen ML; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
  • Appleby BS; From the National Prion Disease Pathology Surveillance Center (D.D.R., A.F., J.B., K.G., M.L.C., B.S.A.) and Department of Population and Quantitative Health Sciences (C.T.), Case Western Reserve University; Departments of Pathology (D.D.R., M.L.C., B.S.A.), Neurology (C.T., M.L.C., B.S.A.), and Psy
Neurology ; 95(8): e1017-e1026, 2020 08 25.
Article en En | MEDLINE | ID: mdl-32571851
OBJECTIVE: To present the National Prion Disease Pathology Surveillance Center's (NPDPSC's) experience using CSF real-time quaking-induced conversion (RT-QuIC) as a diagnostic test, to examine factors associated with false-negative RT-QuIC results, and to investigate the impact of RT-QuICs on prion disease surveillance. METHODS: Between May 2015 and April 2018, the NPDPSC received 10,498 CSF specimens that were included in the study. Sensitivity and specificity analyses were performed on 567 autopsy-verified cases. Prion disease type, demographic characteristics, specimen color, and time variables were examined for association with RT-QuIC results. The effect of including positive RT-QuIC cases in prion disease surveillance was examined. RESULTS: The diagnostic sensitivity and specificity of RT-QuIC across all prion diseases were 90.3% and 98.5%, respectively. Diagnostic sensitivity was lower for fatal familial insomnia, Gerstmann-Sträussler-Scheinker disease, sporadic fatal insomnia, variably protease sensitive prionopathy, and the VV1 and MM2 subtypes of sporadic Creutzfeldt-Jakob disease. Individuals with prion disease and negative RT-QuIC results were younger and had lower tau levels and nonelevated 14-3-3 levels compared to RT-QuIC-positive cases. Sensitivity was high throughout the disease course. Some cases that initially tested RT-QuIC negative had a subsequent specimen test positive. Including positive RT-QuIC cases in surveillance statistics increased laboratory-based case ascertainment of prion disease by 90% over autopsy alone. CONCLUSIONS: RT-QuIC has high sensitivity and specificity for diagnosing prion diseases. Sensitivity limitations are associated with prion disease type, age, and related CSF diagnostic results. RT-QuIC greatly improves laboratory-based prion disease ascertainment for surveillance purposes. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that second-generation RT-QuIC identifies prion disease with a sensitivity of 90.3% and specificity of 98.5% among patients being screened for these diseases due to concerning symptoms.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Biomarcadores / Tamizaje Masivo / Enfermedades por Prión Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Screening_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurology Año: 2020 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Biomarcadores / Tamizaje Masivo / Enfermedades por Prión Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Screening_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurology Año: 2020 Tipo del documento: Article