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

J Neuropathol Exp Neurol. 2016 Jun;75(6):482-98. doi: 10.1093/jnen/nlw033. Epub 2016 May 21.

Abstract

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 (GRN, TMEM106B, ABCC9, 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.

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

Publication types

  • Case Reports
  • Review

MeSH terms

  • Aged, 80 and over
  • Aging / genetics
  • Aging / pathology*
  • Alzheimer Disease / genetics
  • Alzheimer Disease / pathology*
  • Animals
  • DNA-Binding Proteins* / genetics
  • Female
  • Hippocampus / pathology*
  • Humans
  • Sclerosis / genetics
  • Sclerosis / pathology
  • Tauopathies / genetics
  • Tauopathies / pathology*

Substances

  • DNA-Binding Proteins
  • TARDBP protein, human