HIV-associated Neurologic Dysfunction/Dementia Flashcards
Pathophysiology of HIV-associated dementia
- Multifactorial
- HIV-infected monocytes enter the brain and infect microglia, astrocytes, neurons, and oligodendrocytes. Then, the virus may replicate within these cells.
- Toxins and HIV proteins produced by or in response to the presence of HIV may have neurotoxic properties
- The incidence of opportunistic infections and tumors secondary to HIV also plays a role
Neuropsychological testing
A battery of tests to evaluate cognitive impairment more extensively than the MMSE
Effect of HAART on HAD
HAART reduces the incidence and severity of HAD, as one might expect
But, it does not bring these to zero.
Since HAART was only introduced in 1992, and HAART reduces the incidence of HAD . . .
. . . older patients / patients who have had HIV for longer are more likely to have HAD
Presentation/Natural history of HAD
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Early symptoms:
- Difficulty concentrating and with mentation
- Forgetfulness
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As the disease progresses:
- Personality change (apathy, social withdrawal, quietness)
- Psychomotor dysfunction (imbalance, mild ataxia)
- Most common motor symptoms are tripping/falling and poor handwriting
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Late stage disease:
- Disabling ataxia with inability to walk
- Myoclonic jerks, postural tremor
- Bowel and bladder dysfunction
One thing that is NEVER seen in HAD
Focal neurologic deficits
It is a strictly subcortical dementia
Physical exam findings in early vs late HAD
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Early:
- Mostly normal neurologic exam without glaring deficits
- Difficulties in concentration, fine motor manipulation, motor speed
- Mild word finding difficulties and impaired retrieval
- Subtle impairment of rapid limb and eye movements
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Late:
- Hyperreflexia, spasticity, and frontal release signs (UMN signs)
- Apraxia
- Akinetic mutism (severely decreased motor-verbal output)
Imaging findings typical of HAD
Diffuse cerebral atrophy
Sometimes white matter changes and abnormalities are present in the thalamus and basal ganglia
Typical ddx for HAND
- Other forms of dementia (especially FTD and subcortical dementias)
- CNS lymphoma
- PML
- CNS infection
- Toxic-metabolic (B12, thyroid, alcoholism, medication effect, illicit substance use)
Management of HAND is essentially limited to. . .
. . . viral suppression by HAART
HAART can not only protect against, but can also lead to remission of HAND
Antiretrovirals with good CNS penetration are preferred: lamivudine, indinavir, zidovudine
“LIZ, HAND me the HAART”
Risk factors for HAD
- Low CD4 count
- High viral RNA
- Low BMI
- Anemia
- Low level of education