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Neuroimaging correlates with neuropathologic schemes in neurodegenerative disease.
Lowe, Val J; Lundt, Emily S; Albertson, Sabrina M; Przybelski, Scott A; Senjem, Matthew L; Parisi, Joseph E; Kantarci, Kejal; Boeve, Bradley; Jones, David T; Knopman, David; Jack, Clifford R; Dickson, Dennis W; Petersen, Ronald C; Murray, Melissa E.
Afiliação
  • Lowe VJ; Department of Radiology, Mayo Clinic, Rochester, MN, USA. Electronic address: vlowe@mayo.edu.
  • Lundt ES; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Albertson SM; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Przybelski SA; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Senjem ML; Department of Information Technology, Mayo Clinic, Rochester, MN, USA.
  • Parisi JE; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Kantarci K; Department of Radiology, Mayo Clinic, Rochester, MN, USA.
  • Boeve B; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Jones DT; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Knopman D; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Jack CR; Department of Radiology, Mayo Clinic, Rochester, MN, USA.
  • Dickson DW; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Petersen RC; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Murray ME; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Alzheimers Dement ; 15(7): 927-939, 2019 07.
Article em En | MEDLINE | ID: mdl-31175025
ABSTRACT

INTRODUCTION:

Neuroimaging biomarkers are important for early diagnosis of Alzheimer's disease, and comparing multimodality neuroimaging to autopsy data is essential.

METHODS:

We compared the pathologic findings from a prospective autopsy cohort (n = 100) to Pittsburgh compound B PET (PiB-PET), 18F-fluorodeoxyglucose PET (FDG-PET), and MRI. Correlations between neuroimaging biomarkers and neuropathologic schemes were assessed.

RESULTS:

PiB-PET showed strong correlations with Thal amyloid phase and Consortium to Establish a Registry for Alzheimer's Disease score and categorized 44% of Thal phase 1 participants as positive. FDG-PET and MRI correlated modestly with Braak tangle stage in Alzheimer's type pathology. A subset of participants with "none" or "sparse" neuritic plaque scores had elevated PiB-PET signal due to diffuse amyloid plaque. Participants with findings characterized as "suspected non-Alzheimer's pathophysiology" represented 15% of the group.

DISCUSSION:

PiB-PET is associated with Alzheimer's disease, neuritic plaques, and diffuse plaques. FDG-PET and MRI have modest correlation with neuropathologic schemes. Participants with findings characterized as suspected non-Alzheimer's pathophysiology most commonly had primary age-related tauopathy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Emaranhados Neurofibrilares / Placa Amiloide / Doença de Alzheimer / Neuroimagem / Neuropatologia Tipo de estudo: Observational_studies / Risk_factors_studies / Screening_studies Limite: Aged / Aged80 / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Emaranhados Neurofibrilares / Placa Amiloide / Doença de Alzheimer / Neuroimagem / Neuropatologia Tipo de estudo: Observational_studies / Risk_factors_studies / Screening_studies Limite: Aged / Aged80 / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article