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Diagnostic value of plasma phosphorylated tau181 in Alzheimer's disease and frontotemporal lobar degeneration.
Thijssen, Elisabeth H; La Joie, Renaud; Wolf, Amy; Strom, Amelia; Wang, Ping; Iaccarino, Leonardo; Bourakova, Viktoriya; Cobigo, Yann; Heuer, Hilary; Spina, Salvatore; VandeVrede, Lawren; Chai, Xiyun; Proctor, Nicholas K; Airey, David C; Shcherbinin, Sergey; Duggan Evans, Cynthia; Sims, John R; Zetterberg, Henrik; Blennow, Kaj; Karydas, Anna M; Teunissen, Charlotte E; Kramer, Joel H; Grinberg, Lea T; Seeley, William W; Rosen, Howie; Boeve, Bradley F; Miller, Bruce L; Rabinovici, Gil D; Dage, Jeffrey L; Rojas, Julio C; Boxer, Adam L.
Afiliación
  • Thijssen EH; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • La Joie R; Neurochemistry Laboratory, Department of Clinical Chemistry, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam Neuroscience, Amsterdam, the Netherlands.
  • Wolf A; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Strom A; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Wang P; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Iaccarino L; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Bourakova V; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Cobigo Y; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Heuer H; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Spina S; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • VandeVrede L; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Chai X; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Proctor NK; Eli Lilly and Company, Indianapolis, IN, USA.
  • Airey DC; Eli Lilly and Company, Indianapolis, IN, USA.
  • Shcherbinin S; Eli Lilly and Company, Indianapolis, IN, USA.
  • Duggan Evans C; Eli Lilly and Company, Indianapolis, IN, USA.
  • Sims JR; Eli Lilly and Company, Indianapolis, IN, USA.
  • Zetterberg H; Eli Lilly and Company, Indianapolis, IN, USA.
  • Blennow K; Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
  • Karydas AM; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
  • Teunissen CE; Department of Neurodegenerative Disease, University College London Institute of Neurology, Queen Square, London, UK.
  • Kramer JH; UK Dementia Research Institute, University College London, London, UK.
  • Grinberg LT; Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
  • Seeley WW; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
  • Rosen H; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Boeve BF; Neurochemistry Laboratory, Department of Clinical Chemistry, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam Neuroscience, Amsterdam, the Netherlands.
  • Miller BL; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Rabinovici GD; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Dage JL; Department of Pathology, University of California San Francisco, San Francisco, CA, USA.
  • Rojas JC; Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Boxer AL; Department of Pathology, University of California San Francisco, San Francisco, CA, USA.
Nat Med ; 26(3): 387-397, 2020 03.
Article en En | MEDLINE | ID: mdl-32123386
ABSTRACT
With the potential development of new disease-modifying Alzheimer's disease (AD) therapies, simple, widely available screening tests are needed to identify which individuals, who are experiencing symptoms of cognitive or behavioral decline, should be further evaluated for initiation of treatment. A blood-based test for AD would be a less invasive and less expensive screening tool than the currently approved cerebrospinal fluid or amyloid ß positron emission tomography (PET) diagnostic tests. We examined whether plasma tau phosphorylated at residue 181 (pTau181) could differentiate between clinically diagnosed or autopsy-confirmed AD and frontotemporal lobar degeneration. Plasma pTau181 concentrations were increased by 3.5-fold in AD compared to controls and differentiated AD from both clinically diagnosed (receiver operating characteristic area under the curve of 0.894) and autopsy-confirmed frontotemporal lobar degeneration (area under the curve of 0.878). Plasma pTau181 identified individuals who were amyloid ß-PET-positive regardless of clinical diagnosis and correlated with cortical tau protein deposition measured by 18F-flortaucipir PET. Plasma pTau181 may be useful to screen for tau pathology associated with AD.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas tau / Degeneración Lobar Frontotemporal / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Prognostic_studies Aspecto: Patient_preference Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Med Asunto de la revista: BIOLOGIA MOLECULAR / MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas tau / Degeneración Lobar Frontotemporal / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Prognostic_studies Aspecto: Patient_preference Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Med Asunto de la revista: BIOLOGIA MOLECULAR / MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA