Dementia: Core Definition & Epidemiology
Dementia is a clinical syndrome of progressive cognitive decline severe enough to impair daily functioning. It is not a single disease — it is an umbrella term covering multiple pathological subtypes. Globally affects 57 million; GCC nations face a rapidly rising burden linked to ageing populations and the vascular risk factor epidemic (diabetes, hypertension, obesity).
Alzheimer's Disease (AD) 60–70% of cases
Pathophysiology
- Amyloid plaques (extracellular β-amyloid) — earliest biomarker
- Neurofibrillary tangles (intracellular hyperphosphorylated tau)
- Acetylcholine deficit → basis for pharmacotherapy
- Hippocampal atrophy first, then parietal/temporal
Clinical Features
- Insidious onset, gradual progression
- Memory loss is predominant early feature (episodic memory first)
- Later: aphasia, apraxia, agnosia, executive dysfunction
Investigations
- CT/MRI: medial temporal lobe/hippocampal atrophy
- MMSE, MoCA for staging
- CSF: low Aβ42, high total-tau / phospho-tau
- PET amyloid imaging (specialist centres)
Vascular Dementia (VaD) 15–20% of cases
Pathophysiology
- Cerebrovascular disease: multiple infarcts, single strategic infarct, or diffuse white matter disease (Binswanger's)
- Vascular risk factors: HTN, DM, smoking, AF, hyperlipidaemia
Clinical Features
- Stepwise decline rather than gradual
- Focal neurological signs common
- Gait disturbance, urinary incontinence early
- Executive dysfunction may precede memory loss
Investigations
- MRI: white matter hyperintensities (leukoaraiosis), lacunar infarcts
- Vascular risk factor workup: HbA1c, lipids, BP monitoring, ECG (AF)
- Carotid Doppler if indicated
Lewy Body Dementia (LBD) ~5%
Core Features (must have ≥2 for probable LBD)
- Fluctuating cognition with pronounced variations in attention
- Visual hallucinations (recurrent, detailed, well-formed)
- Parkinsonism (spontaneous, not drug-induced)
- REM sleep behaviour disorder
Investigations
- DaTSCAN (dopamine transporter SPECT) — abnormal in LBD, normal in AD
- Polysomnography for REM sleep behaviour disorder
Frontotemporal Dementia (FTD)
Key Distinctions from AD
- Younger onset (50s–60s vs 70s+ in AD)
- Personality and behaviour change predominates early — disinhibition, apathy, social inappropriateness, hypersexuality, compulsive rituals
- Memory relatively preserved early
- Language variants: progressive non-fluent aphasia, semantic dementia
- Frontal/temporal lobe atrophy on MRI; pick bodies (tau)
FTD vs Alzheimer's
| Feature | FTD | AD |
|---|---|---|
| Onset age | Usually <65 | Usually >65 |
| Early symptom | Behaviour/personality | Episodic memory |
| MRI atrophy | Frontal/temporal | Medial temporal |
| MMSE | May be relatively preserved | Early impairment |
Mixed Dementia & Reversible Causes
Mixed Dementia
Most commonly AD + vascular pathology. Very prevalent in post-mortem studies. Clinical features overlap. Manage both vascular risk factors and cognitive symptoms.
Reversible ("Potentially Treatable") Causes — MUST EXCLUDE
- Hypothyroidism — TFTs mandatory in all
- Vitamin B12 / folate deficiency
- Neurosyphilis — syphilis serology
- Subdural haematoma — CT head
- Normal Pressure Hydrocephalus (NPH) — triad: gait apraxia + urinary incontinence + cognitive decline; CT: ventriculomegaly; shunting may help
- Alcohol-related brain damage, Wernicke's encephalopathy (thiamine)
- Medication toxicity (anticholinergics, benzodiazepines)
- Depression (pseudodementia)
- HIV dementia
NICE Diagnostic Pathway (NG97)
- History from patient + carer (collateral history essential)
- Cognitive assessment (MMSE or MoCA) at presentation
- Blood tests to exclude reversible causes: FBC, U&E, LFTs, TFTs, glucose, B12/folate, calcium, syphilis serology
- Structural brain imaging (CT or MRI) — exclude tumour, subdural, NPH, infarcts
- Specialist memory clinic assessment if uncertain diagnosis
- Diagnosis disclosure — compassionately, with written information
- Care plan — including advance care planning discussion