Alzheimer's%20disease%20-and-%20dementia Diagnosis
Diagnosis
- In order for a diagnosis of dementia to be made, the cognitive impairment should be sufficient to cause a decline in the occupational and social functioning of the individual
Diagnostic Guidelines
- Diagnosis of subtype of dementia is done by using international standard criteria (DSM-5)
- Clinical assessment is the basis of diagnosis
- Neuropsychological testing is used when dementia is not clinically obvious
Alzheimer’s Disease
- Diagnosis of Alzheimer’s disease should be made when typical degenerative syndrome is present
- Definitive diagnosis is only confirmed on microscopic exam of the brain (usually at autopsy)
- MRI findings of hippocampal atrophy (medial temporal atrophy) and/or global cortical atrophy may help in the diagnosis of Alzheimer’s disease in a patient with typical clinical presentation
- Amyloid positron emission tomography (PET) scan and cerebrospinal fluid amyloid and tau levels may help in the diagnosis of Alzheimer's disease
Vascular Dementia
- Diagnosed by history, focal neurological signs and symptoms and/or imaging studies with clear evidence of cerebrovascular events
Dementia with Lewy Bodies
- Histopathologically, Lewy inclusion bodies are present in the cerebral cortex
- May be diagnosed on history, physical and neurological examination, and ancillary procedures, such as structural MRI, brain fluorodeoxyglucose (FDG)-PET scan, Dopamine Transporter single-photon emission computed tomography (SPECT) scan and metaiodobenzylguanidine (MIBG) myocardial scintigraphy
- MRI will show absent or minimal medial temporal lobe atrophy, generalized cortical atrophy with relatively normal hippocampal size
Assessment
Clinical Assessment
Should include, but is not limited to, the following:
- Careful evaluation of medical, psychiatric, neurological, medication and social history
- Detailed review of cognitive and behavioral symptoms from patient and caregiver
Physical Examination
- Exclude treatable causes which may be contributing to dementia
- Neuropsychological and neuropsychiatric assessment
Laboratory Tests
Diagnostic Tests
- Complete blood count (CBC), serum electrolytes, liver function test, renal function tests, glucose, thyroid function, vitamin B12 and folate levels, and syphilis serology (if syphilis is suspected)
- Electroencephalography (EEG) may be useful if suspicious of CJD, underlying seizure disorder or in delirium
- Neuroimaging [magnetic resonance imaging (MRI), computed tomography (CT) scan]
- Helps to determine dementia subtypes and rule out intra-cerebral pathology
- Brain MRI is the preferred modality to assist with early diagnosis and detect subcortical vascular changes
- Brain CT or MRI should be performed in hypertensive patients with cognitive decline to detect silent infarct, microbleed, or white matter lesion
- Neuropsychological testing
- Determination of cerebrospinal fluid (CSF) biomarkers and plasma markers are not recommended in the diagnosis of mild cognitive impairment
- Genetic testing and use of genetic marker APOE with or without plasma lipid is not routinely recommended
Cognitive and Mental State Examination
- Montreal Cognitive Assessment, 7-Minute Screen, Memory Impairment Screen, Mini-Mental State Exam, Abbreviated Mental Test or Clock Drawing Test
- Score interpretations should also consider other factors that may affect the performance (eg educational level, social class, cultural background, literacy, language or other communication difficulties)
- Refer to memory clinic with multidisciplinary collaborative care for early and accurate diagnosis and management of dementia