Your browser doesn't support javascript.
loading
Distinct tau PET patterns in atrophy-defined subtypes of Alzheimer's disease.
Ossenkoppele, Rik; Lyoo, Chul Hyoung; Sudre, Carole H; van Westen, Danielle; Cho, Hanna; Ryu, Young Hoon; Choi, Jae Yong; Smith, Ruben; Strandberg, Olof; Palmqvist, Sebastian; Westman, Eric; Tsai, Richard; Kramer, Joel; Boxer, Adam L; Gorno-Tempini, Maria L; La Joie, Renaud; Miller, Bruce L; Rabinovici, Gil D; Hansson, Oskar.
Afiliación
  • Ossenkoppele R; Lund University, Clinical Memory Research Unit, Lund, Sweden.
  • Lyoo CH; Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
  • Sudre CH; Department of Neurology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
  • van Westen D; School of Biomedical Engineering and Imaging Sciences King's College London, London, United Kingdom.
  • Cho H; Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, United Kingdom.
  • Ryu YH; Centre for Medical Image Computing, Department of Medical Physics, University College London, United Kingdom.
  • Choi JY; Lund University, Diagnostic Radiology, Lund, Sweden.
  • Smith R; Department of Neurology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
  • Strandberg O; Lund University, Diagnostic Radiology, Lund, Sweden.
  • Palmqvist S; Department of Nuclear Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
  • Westman E; Division of RI-Convergence Research, Korea Institute Radiological and Medical Sciences, Seoul, South Korea.
  • Tsai R; Lund University, Clinical Memory Research Unit, Lund, Sweden.
  • Kramer J; Lund University, Clinical Memory Research Unit, Lund, Sweden.
  • Boxer AL; Lund University, Clinical Memory Research Unit, Lund, Sweden.
  • Gorno-Tempini ML; Division of Clinical Geriatrics, Department of Neurobiology, Karolinska Institute, Care Sciences and Society, Stockholm, Sweden.
  • La Joie R; Department of Neurology, University of California San Francisco, Memory and Aging Center, San Francisco, USA.
  • Miller BL; Department of Neurology, University of California San Francisco, Memory and Aging Center, San Francisco, USA.
  • Rabinovici GD; Division of Clinical Geriatrics, Department of Neurobiology, Karolinska Institute, Care Sciences and Society, Stockholm, Sweden.
  • Hansson O; Department of Neurology, University of California San Francisco, Memory and Aging Center, San Francisco, USA.
Alzheimers Dement ; 16(2): 335-344, 2020 02.
Article en En | MEDLINE | ID: mdl-31672482
ABSTRACT

INTRODUCTION:

Differential patterns of brain atrophy on structural magnetic resonance imaging (MRI) revealed four reproducible subtypes of Alzheimer's disease (AD) (1) "typical", (2) "limbic-predominant", (3) "hippocampal-sparing", and (4) "mild atrophy". We examined the neurobiological characteristics and clinical progression of these atrophy-defined subtypes.

METHODS:

The four subtypes were replicated using a clustering method on MRI data in 260 amyloid-ß-positive patients with mild cognitive impairment or AD dementia, and we subsequently tested whether the subtypes differed on [18 F]flortaucipir (tau) positron emission tomography, white matter hyperintensity burden, and rate of global cognitive decline.

RESULTS:

Voxel-wise and region-of-interest analyses revealed the greatest neocortical tau load in hippocampal-sparing (frontoparietal-predominant) and typical (temporal-predominant) patients, while limbic-predominant patients showed particularly high entorhinal tau. Typical patients with AD had the most pronounced white matter hyperintensity load, and hippocampal-sparing patients showed the most rapid global cognitive decline.

DISCUSSION:

Our data suggest that structural MRI can be used to identify biologically and clinically meaningful subtypes of AD.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Atrofia / Proteínas tau / Tomografía de Emisión de Positrones / Enfermedad de Alzheimer Tipo de estudio: Prognostic_studies Límite: Aged / Female / Humans / Middle aged Idioma: En Revista: Alzheimers Dement Año: 2020 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Atrofia / Proteínas tau / Tomografía de Emisión de Positrones / Enfermedad de Alzheimer Tipo de estudio: Prognostic_studies Límite: Aged / Female / Humans / Middle aged Idioma: En Revista: Alzheimers Dement Año: 2020 Tipo del documento: Article País de afiliación: Suecia