4.5 Article

Non-Verbal Episodic Memory Deficits in Primary Progressive Aphasias are Highly Predictive of Underlying Amyloid Pathology

Journal

JOURNAL OF ALZHEIMERS DISEASE
Volume 51, Issue 2, Pages 367-376

Publisher

IOS PRESS
DOI: 10.3233/JAD-150752

Keywords

Logopenic progressive aphasia; memory; Pittsburgh Compound B; primary progressive aphasia; progressive nonfluent aphasia

Categories

Funding

  1. National Health and Medical Research Council (NHMRC) [APP1037746]
  2. Australian Research Council (ARC) Centre of Excellence in Cognition and its Disorders [CE11000102]
  3. Alzheimer's Research UK
  4. Wellcome Trust
  5. Newton Trust
  6. NHMRC program
  7. ARC Centre of Excellence in Cognition and its Disorders
  8. DVC postdoctoral Fellowship, University of Sydney, Australia
  9. NHMRC
  10. GE Healthcare
  11. Avid Radiopharmaceuticals
  12. Piramal Imaging
  13. Navidea
  14. NHMRC research grant

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Diagnostic distinction of primary progressive aphasias (PPA) remains challenging, in particular for the logopenic (lvPPA) and nonfluent/agrammatic (naPPA) variants. Recent findings highlight that episodic memory deficits appear to discriminate these PPA variants from each other, as only lvPPA perform poorly on these tasks while having underlying amyloid pathology similar to that seen in amnestic dementias like Alzheimer's disease (AD). Most memory tests are, however, language based and thus potentially confounded by the prevalent language deficits in PPA. The current study investigated this issue across PPA variants by contrasting verbal and non-verbal episodic memory measures while controlling for their performance on a language subtest of a general cognitive screen. A total of 203 participants were included (25 lvPPA; 29 naPPA; 59 AD; 90 controls) and underwent extensive verbal and non-verbal episodic memory testing, with a subset of patients (n = 45) with confirmed amyloid profiles as assessed by Pittsburgh Compound B and PET. The most powerful discriminator between naPPA and lvPPA patients was a non-verbal recall measure (Rey Complex Figure delayed recall), with 81% of PPA patients classified correctly at presentation. Importantly, AD and lvPPA patients performed comparably on this measure, further highlighting the importance of underlying amyloid pathology in episodic memory profiles. The findings demonstrate that non-verbal recall emerges as the best discriminator of lvPPA and naPPA when controlling for language deficits in high load amyloid PPA cases.

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