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Alzheimer's Disease

Tests
There are no laboratory tests available that will positively diagnose Alzheimer’s Disease (AD) during life. Currently, the only definite diagnosis of AD is to microscopically examine a section of the patient’s brain tissue after death. Pathologists look for senile plaques and neurofibrillary tangles characteristic of AD. Since plaque and tangle formation is also seen in normal aging, the sample must be compared to a control sample (normal, non-AD brain tissue) from a person the same age as the patient.

However, doctors currently can make a reasonably accurate clinical diagnosis of AD using a variety of tests and procedures to rule out other causes for dementia. When a patient presents with symptoms of dementia, the doctor will evaluate his or her personal and family history (preferably of several generations); perform a physical exam; determine the age of onset, and give the patient neuropsychological tests to measure his or her memory, language skills, and other cognitive functions. The doctor may use a range of traditional laboratory tests to rule out deficiencies and other diseases and conditions that could be affecting the patient’s memory. They will also look for overmedication and may use imaging tools, such as computed tomography (CT) and magnetic resonance imaging (MRI) scans, to look for evidence of trauma, tumors, and stroke that could be causing dementia and to look for brain atrophy (shrinkage, usually only seen later in the Alzheimer’s Disease progression). If the doctor suspects AD, they may do other less common laboratory tests (see Table) to differentiate between AD and other forms of dementia and to check for genetic risk factors.

Tests to Aid in Categorization of Dementia

Test

Sample

Use

Associated with

Common Lab Tests

 

 

 

Vitamin B12

Blood

Rule out AD

B12 deficiency

T4

Blood

Rule out AD

Thyroid function

TSH

Blood

Rule out AD

Thyroid function

CBC

Blood

Rule out AD

Anemia, infection

Electrolytes

Blood

Rule out AD

Na+,K+,Cl-,CO2 and pH balance

ESR

Blood

Rule out AD

Inflammation

HIV antibody

Blood

Rule out AD

AIDS

RPR

Blood

Rule out AD

Syphilis

Drug Screen

Urine

Rule out AD

Illicit drug use

 

 

 

 

Imaging Tests

 

 

 

CT (computed tomography)

Body scan

Rule out AD or with late stage AD

stroke and brain atrophy (shrinkage associated with late stage AD)

MRI (magnetic resonance imaging)

Body scan

Rule out AD or with late stage AD

stroke and brain atrophy (shrinkage associated with late stage AD)

 

 

 

 

Less Common Lab Tests

 

 

 

Amyloid Beta 42 peptide and Tau protein correlation (Tau/Ab42)

CSF (cerebro-spinal fluid)

Help differentiate AD from other dementias

In symptomatic patients, decreased Ab42 level along with an elevated Tau protein level indicates an increased likelihood of AD, regardless of the cause

ApoE genotype

Blood

Determine ApoE genotype and adjunct test to confirm/rule out probable AD

ApoE e4 associated with increased risk of late onset AD in symptomatic patients; e4 and e2 variations also associated with lipid disorders

PSEN1

Blood

Test for genetic mutation

Thought to cause about half of the cases of Early Onset Familial AD

PSEN2

Blood, available in only a few labs

Test for genetic mutation; available in only a few labs

Early Onset Familial AD; mutation very rare, identified in only a few family lines

APP

Blood

Test for genetic mutation; still in research - not clinically available

Early Onset Familial AD; mutation very rare, identified in only a few family lines

 


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This article last reviewed on August 19, 2005.
 
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