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Fluid and PET biomarkers for amyloid pathology in Alzheimer's disease.
Cohen, Ann D; Landau, Susan M; Snitz, Beth E; Klunk, William E; Blennow, Kaj; Zetterberg, Henrik.
Afiliação
  • Cohen AD; Department of Psychiatry, University of Pittsburgh School of Medicine, United States of America. Electronic address: cohenad@upmc.edu.
  • Landau SM; Neurology Helen Wills Neuroscience Institute, University of California, Berkeley, United States of America; Lawrence Berkeley National Laboratory, Molecular Biophysics and Integrated Bioimaging Functional Imaging Department, Life Sciences Division, United States of America.
  • Snitz BE; Department of Neurology, University of Pittsburgh School of Medicine, United States of America.
  • Klunk WE; Department of Psychiatry, University of Pittsburgh School of Medicine, United States of America.
  • Blennow K; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Molndal, Sweden; Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, University College, London, United Kingdom of Great Britain and Northern I
  • Zetterberg H; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Molndal, Sweden; Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, University College, London, United Kingdom of Great Britain and Northern I
Mol Cell Neurosci ; 97: 3-17, 2019 06.
Article em En | MEDLINE | ID: mdl-30537535
Alzheimer's disease (AD) is characterized by amyloid plaques and tau pathology (neurofibrillary tangles and neuropil threads). Amyloid plaques are primarily composed of aggregated and oligomeric ß-amyloid (Aß) peptides ending at position 42 (Aß42). The development of fluid and PET biomarkers for Alzheimer's disease (AD), has allowed for detection of Aß pathology in vivo and marks a major advancement in understanding the role of Aß in Alzheimer's disease (AD). In the recent National Institute on Aging and Alzheimer's Association (NIA-AA) Research Framework, AD is defined by the underlying pathology as measured in patients during life by biomarkers (Jack et al., 2018), while clinical symptoms are used for staging of the disease. Therefore, sensitive, specific and robust biomarkers to identify brain amyloidosis are central in AD research. Here, we discuss fluid and PET biomarkers for Aß and their application.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Encéfalo / Peptídeos beta-Amiloides / Tomografia por Emissão de Pósitrons / Doença de Alzheimer Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Encéfalo / Peptídeos beta-Amiloides / Tomografia por Emissão de Pósitrons / Doença de Alzheimer Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article