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Metabolic Topology of Neurodegenerative Disorders: Influence of Cognitive and Motor Deficits.
Granert, Oliver; Drzezga, Alexander E; Boecker, Henning; Perneczky, Robert; Kurz, Alexander; Götz, Julia; van Eimeren, Thilo; Häussermann, Peter.
Afiliação
  • Granert O; Department of Neurology, Kiel University, Kiel, Germany o.granert@neurologie.uni-kiel.de.
  • Drzezga AE; Department of Nuclear Medicine, University of Cologne, Cologne, Germany.
  • Boecker H; Department of Radiology, Bonn University, Bonn, Germany.
  • Perneczky R; Neuroepidemiology and Ageing Research Unit, Imperial College of Science, Technology and Medicine, London, United Kingdom Cognitive Impairment and Dementia Services, West London Mental Health NHS Trust, London, United Kingdom Department of Psychiatry, TU Munich, Munich, Germany.
  • Kurz A; Department of Psychiatry, TU Munich, Munich, Germany.
  • Götz J; Department of Neurology, Kiel University, Kiel, Germany.
  • van Eimeren T; Department of Neurology, Kiel University, Kiel, Germany.
  • Häussermann P; Department of Psychiatry, Kiel University, Kiel, Germany; and LVR Clinic Cologne, Academic Teaching Hospital, University of Cologne, Cologne, Germany.
J Nucl Med ; 56(12): 1916-21, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26383147
ABSTRACT
UNLABELLED Parkinson disease with and without dementia (PDD and PD, respectively), dementia with Lewy bodies (DLB), and Alzheimer dementia (AD) traditionally have been viewed as distinct clinical and pathologic entities. However, intriguing overlaps in biochemical, clinical, and imaging findings question the concept of distinct entities and suggest a continuous spectrum in which individual patients express PD-typical patterns and AD-typical patterns to a variable degree.

METHODS:

Following this concept, we built a topological map based on regional patterns of the cerebral metabolic rate of glucose as measured with (18)F-FDG PET to rank and localize single subjects' disease status according to PD-typical (PD vs. controls) and AD-typical (AD vs. controls) pattern expression in patients clinically characterized as PD, PDD, DLB, amnestic mild cognitive impairment, and AD.

RESULTS:

The topology generally confirmed an indivisible spectrum of disease manifestation according to 2 separable expression patterns. The expression values derived from the first pattern were highly correlated with individual cognitive, but not motor, disability. The opposite was found for the corresponding expression values of the second pattern.

CONCLUSION:

The metabolic imaging analysis supports the notion that there is a continuous spectrum of neurodegeneration between AD and PD. Furthermore, PDD and DLB may in fact represent 1 overlapping disease entity, characterized by the presence of mixed neuropathology and only different by the time course.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cognição / Doenças Neurodegenerativas / Transtornos dos Movimentos Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cognição / Doenças Neurodegenerativas / Transtornos dos Movimentos Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article