Table 7.
Subtype | Characteristics |
---|---|
Associated with advanced age (HS-Ageing and HS-Ageing–TPD) | Highest prevalence in ‘oldest-old’a |
Aberrant TDP-43 in ∼90% of casesa | |
TDP-43 bilateral even if routine haematoxylin and eosin histology not | |
Still not known whether TPD-43 is causative | |
No proven relation to strokea | |
Dementia, not usually seizuresa | |
Association with Alzheimer’s disease is weak or non-existenta | |
APOE alleles do not alter riska | |
Cognitive tests: word list delay/verbal fluency ratio | |
With seizures (HS–Sz) | Younger persons |
Seizures, not usually dementia | |
Often unilateral | |
No aberrant TDP-43a | |
With tauopathy (HS–tau) | Non-Alzheimer’s disease tauopathy |
May include argyrophilic grain disease or progressive supranuclear palsy | |
With non-tauopathy frontotemporal dementia (HS–FTD) | Multiple possible aetiologies |
Accompanied by frontotemporal dementia clinical syndrome | |
With cerebrovascular disease (HS–CVD) | May coexist with other cerebrovascular sequelae |
Probably not progressive | |
Similar pathology can be seen in hypoglycaemia, trauma |
a Focus of current study.