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Investigating the clinico-anatomical dissociation in the behavioral variant of Alzheimer disease.
Singleton, Ellen H; Pijnenburg, Yolande A L; Sudre, Carole H; Groot, Colin; Kochova, Elena; Barkhof, Frederik; La Joie, Renaud; Rosen, Howard J; Seeley, William W; Miller, Bruce; Cardoso, M Jorge; Papma, Janne; Scheltens, Philip; Rabinovici, Gil D; Ossenkoppele, Rik.
Afiliação
  • Singleton EH; Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands. e.singleton@amsterdamumc.nl.
  • Pijnenburg YAL; Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
  • Sudre CH; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Groot C; Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
  • Kochova E; Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
  • Barkhof F; Department of Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
  • La Joie R; Center for Medical Image Computing, Department of Medical Physics and Biomedical Engineering, University College London, London, UK.
  • Rosen HJ; Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, USA.
  • Seeley WW; Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, USA.
  • Miller B; Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, USA.
  • Cardoso MJ; Department of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, USA.
  • Papma J; School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
  • Scheltens P; Translational Imaging Group, CMIC, Department of Medical Physics and Biomedical Engineering, University College London, London, UK.
  • Rabinovici GD; Department of Neurology, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Ossenkoppele R; Department of Radiology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Alzheimers Res Ther ; 12(1): 148, 2020 11 14.
Article em En | MEDLINE | ID: mdl-33189136
ABSTRACT

BACKGROUND:

We previously found temporoparietal-predominant atrophy patterns in the behavioral variant of Alzheimer's disease (bvAD), with relative sparing of frontal regions. Here, we aimed to understand the clinico-anatomical dissociation in bvAD based on alternative neuroimaging markers.

METHODS:

We retrospectively included 150 participants, including 29 bvAD, 28 "typical" amnestic-predominant AD (tAD), 28 behavioral variant of frontotemporal dementia (bvFTD), and 65 cognitively normal participants. Patients with bvAD were compared with other diagnostic groups on glucose metabolism and metabolic connectivity measured by [18F]FDG-PET, and on subcortical gray matter and white matter hyperintensity (WMH) volumes measured by MRI. A receiver-operating-characteristic-analysis was performed to determine the neuroimaging measures with highest diagnostic accuracy.

RESULTS:

bvAD and tAD showed predominant temporoparietal hypometabolism compared to controls, and did not differ in direct contrasts. However, overlaying statistical maps from contrasts between patients and controls revealed broader frontoinsular hypometabolism in bvAD than tAD, partially overlapping with bvFTD. bvAD showed greater anterior default mode network (DMN) involvement than tAD, mimicking bvFTD, and reduced connectivity of the posterior cingulate cortex with prefrontal regions. Analyses of WMH and subcortical volume showed closer resemblance of bvAD to tAD than to bvFTD, and larger amygdalar volumes in bvAD than tAD respectively. The top-3 discriminators for bvAD vs. bvFTD were FDG posterior-DMN-ratios (bvADbvFTD, area under the curve [AUC] range 0.85-0.91, all p < 0.001). The top-3 for bvAD vs. tAD were amygdalar volume (bvAD>tAD), MRI anterior-DMN-ratios (bvADAUC range 0.71-0.84, all p < 0.05).

CONCLUSIONS:

Subtle frontoinsular hypometabolism and anterior DMN involvement may underlie the prominent behavioral phenotype in bvAD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Demência Frontotemporal / Doença de Alzheimer Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Demência Frontotemporal / Doença de Alzheimer Idioma: En Ano de publicação: 2020 Tipo de documento: Article