Frontotemporal dementia
Frontotemporal lobar degeneration (tau/TDP-43; Pick bodies)
Overview
An early-onset dementia (often <65) from frontal/temporal lobar degeneration, presenting with EARLY personality/behavioural change or progressive language breakdown, with memory relatively preserved early on — the opposite emphasis to Alzheimer.
Recognise
- Behavioural variant (Pick disease): disinhibition, apathy, loss of empathy, compulsive/repetitive behaviour, overeating
- Primary progressive aphasia variants: non-fluent or semantic language breakdown
- Younger onset (45–65), relatively preserved early memory; frontal/temporal atrophy
Red flags
- Early-onset dementia with personality change — often misattributed to a psychiatric disorder
Differentials & how to tell them apart
Investigations
Cognitive testing (frontal/executive + language); MRI (frontal/temporal atrophy); exclude reversible causes; specialist neuropsychology.
Management
Supportive + behavioural management (SSRIs for behaviour); cholinesterase inhibitors NOT used
- 1Specialist diagnosis; behavioural and environmental management, carer support and safety planning.Gate: Cholinesterase inhibitors are NOT recommended in FTD (may worsen it) — manage behaviour with SSRIs and non-drug strategies
- 2Address risk (driving, finances, safeguarding); SALT for language variants; genetic counselling where familial.
Key points
Early behaviour/personality or language change in a younger patient with spared memory = FTD. It is the great mimic of a new psychiatric illness in middle age.
Monitor & prognosis
Behaviour, language, safety, carer strain.
Progressive; shorter survival than Alzheimer.
Source: NICE NG97 (dementia)