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Neuroimaging correlates of Stages of Objective Memory Impairment (SOMI) system.
Grober, Ellen; Papp, Kathryn V; Rentz, Dorene M; Sperling, Reisa A; Johnson, Keith A; Amariglio, Rebecca E; Schultz, Aaron; Lipton, Richard B; Ezzati, Ali.
Afiliación
  • Grober E; Department of Neurology Albert Einstein College of Medicine and Montefiore Medical Center Bronx New York USA.
  • Papp KV; Harvard Aging Brain Study Department of Neurology Massachusetts General Hospital Harvard Medical School Boston Massachusetts USA.
  • Rentz DM; Center for Alzheimer Research and Treatment Department of Neurology Brigham and Women's Hospital Boston Massachusetts USA.
  • Sperling RA; Harvard Aging Brain Study Department of Neurology Massachusetts General Hospital Harvard Medical School Boston Massachusetts USA.
  • Johnson KA; Center for Alzheimer Research and Treatment Department of Neurology Brigham and Women's Hospital Boston Massachusetts USA.
  • Amariglio RE; Harvard Aging Brain Study Department of Neurology Massachusetts General Hospital Harvard Medical School Boston Massachusetts USA.
  • Schultz A; Center for Alzheimer Research and Treatment Department of Neurology Brigham and Women's Hospital Boston Massachusetts USA.
  • Lipton RB; Harvard Aging Brain Study Department of Neurology Massachusetts General Hospital Harvard Medical School Boston Massachusetts USA.
  • Ezzati A; Center for Alzheimer Research and Treatment Department of Neurology Brigham and Women's Hospital Boston Massachusetts USA.
Alzheimers Dement (Amst) ; 13(1): e12224, 2021.
Article en En | MEDLINE | ID: mdl-35005192
ABSTRACT

INTRODUCTION:

To assess the relationship between memory performance defined by the Stages of Objective Memory Impairment (SOMI) system and the Alzheimer's disease (AD) ATN (amyloid beta [A], pathologic tau [T], and neurodegeneration [N]) biomarker system.

METHODS:

We used data from the Harvard Aging Brain Study cohort to estimate the level of ATN biomarkers amyloid beta (C-Pittsburgh compound B-positron emission tomography [PET]), tau (F-18-flortaucipir [FTP] PET), and neurodegeneration (magnetic resonance imaging volumetrics). We assessed the cross-sectional relationship of SOMI classification with global amyloid levels, entorhinal and inferior temporal tau deposition, and hippocampal atrophy.

RESULTS:

Participants with both memory storage and retrieval deficits (SOMI-3, -4) had smaller hippocampal volumes and higher entorhinal and inferior temporal tau burden than participants with no memory impairment (SOMI-0) or mild retrieval difficulty (SOMI-1). Amyloid burden did not differ among SOMI stages.

DISCUSSION:

This pilot supports the close relationship between tau pathology and memory impairment across the AD continuum.  SOMI may be useful to determine eligibility for randomized controlled trials prior to the assessment of biomarker status.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Alzheimers Dement (Amst) Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Alzheimers Dement (Amst) Año: 2021 Tipo del documento: Article
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