4.3 Review

New Old Pathologies: AD, PART, and Cerebral Age-Related TDP-43 With Sclerosis (CARTS)

Journal

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/jnen/nlw033

Keywords

Arteriosclerosis; Cerebrovascular disease; Frontotemporal lobar degeneration; Genome-wide association study; Neurofibrillary tangles; Plaques; VCID

Funding

  1. NIA NIH HHS [P30 AG010124, U19 AG010483, U01 AG016976, P30 AG028383, K25 AG043546, P01 AG017586] Funding Source: Medline
  2. NINDS NIH HHS [F30 NS090714] Funding Source: Medline

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The pathology-based classification of Alzheimer's disease (AD) and other neurodegenerative diseases is a work in progress that is important for both clinicians and basic scientists. Analyses of large autopsy series, biomarker studies, and genomics analyses have provided important insights about AD and shed light on previously unrecognized conditions, enabling a deeper understanding of neurodegenerative diseases in general. After demonstrating the importance of correct disease classification for AD and primary age-related tauopathy, we emphasize the public health impact of an underappreciated AD mimic, which has been termed hippocampal sclerosis of aging or hippocampal sclerosis dementia. This pathology affects > 20% of individuals older than 85 years and is strongly associated with cognitive impairment. In this review, we provide an overview of current hypotheses about how genetic risk factors (BCC9, and KCNMB2), and other pathogenetic influences contribute to TDP-43 pathology and hippocampal sclerosis. Because hippocampal sclerosis of aging affects the oldest-old with arteriolosclerosis and TDP-43 pathologies that extend well beyond the hippocampus, more appropriate terminology for this disease is required. We recommend cerebral age-related TDP-43 and sclerosis (CARTS). A detailed case report is presented, which includes neuroimaging and longitudinal neurocognitive data. Finally, we suggest a neuropathology-based diagnostic rubric for CARTS.

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