Your browser doesn't support javascript.
loading
Assessment of amyloid ß in pathologically confirmed frontotemporal dementia syndromes.
Tan, Rachel H; Kril, Jillian J; Yang, Yue; Tom, Nicole; Hodges, John R; Villemagne, Victor L; Rowe, Christopher C; Leyton, Cristian E; Kwok, John B J; Ittner, Lars M; Halliday, Glenda M.
Afiliação
  • Tan RH; Brain and Mind Centre, Sydney Medical School, The University of Sydney, Sydney, Australia.
  • Kril JJ; School of Medical Sciences, University of New South Wales, Sydney, Australia.
  • Yang Y; Neuroscience Research Australia, Sydney, Australia.
  • Tom N; Discipline of Pathology, Sydney Medical School, The University of Sydney, Sydney, Australia.
  • Hodges JR; Brain and Mind Centre, Sydney Medical School, The University of Sydney, Sydney, Australia.
  • Villemagne VL; Neuroscience Research Australia, Sydney, Australia.
  • Rowe CC; Neuroscience Research Australia, Sydney, Australia.
  • Leyton CE; Brain and Mind Centre, Sydney Medical School, The University of Sydney, Sydney, Australia.
  • Kwok JBJ; School of Medical Sciences, University of New South Wales, Sydney, Australia.
  • Ittner LM; Neuroscience Research Australia, Sydney, Australia.
  • Halliday GM; Department of Molecular Imaging and Therapy, Centre for PET, Austin Health, Melbourne, Australia.
Alzheimers Dement (Amst) ; 9: 10-20, 2017.
Article em En | MEDLINE | ID: mdl-28653036
ABSTRACT

INTRODUCTION:

The diagnostic utility of in vivo amyloid ß (Aß) imaging to aid in the clinical distinction between frontotemporal dementia (FTD) and Alzheimer's disease remains unclear without data on the prevalence and severity of Aß in pathologically confirmed FTD syndromes.

METHODS:

Aß was assessed in 98 autopsy-confirmed FTD and 36 control cases, and the pathological accuracy of 11C-Pittsburgh compound B (PiB)-positron emission tomography imaging was assessed in a subset of FTD cases (n = 15).

RESULTS:

Aß was identified in a similar proportion of FTD syndromes and age-matched controls and increases with age. Alzheimer's disease pathology was identified in all cases with high PiB retention and in one case with low PiB retention. We further demonstrate a strong regional correlation between volume fraction of histological Aß with PiB standard uptake value ratio scaled to the white matter.

DISCUSSION:

The present study provides a pathologic reference to assist in the interpretation of in vivo assessments in FTD syndromes.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article