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Published on: September 3, 2021
Rivastigmine for HIV-associated neurocognitive disorders: a randomized crossover pilot study
Samanta Simioni1, Matthias Cavassini, Jean-Marie Annoni
1Department of Neurology, CHUV, Lausanne, Switzerland.
Rivastigmine did not improve cognitive function in long-lasting aviremic HIV+ patients with HIV-associated neurocognitive disorders (HAND). However, it showed a benefit in psychomotor speed, suggesting further research with transdermal rivastigmine is warranted.
Area of Science:
- Neuroscience
- Pharmacology
- Infectious Diseases
Background:
- HIV-associated neurocognitive disorders (HAND) remain a challenge despite effective antiretroviral therapy.
- Cognitive deficits in HAND can significantly impact patients' quality of life and daily functioning.
- Acetylcholinesterase inhibitors, like rivastigmine, are used for other neurodegenerative conditions and are being explored for HAND.
Purpose of the Study:
- To evaluate the efficacy and safety of oral rivastigmine in treating HAND.
- To assess rivastigmine's impact on cognitive function, specifically processing speed, attention, executive function, and motor skills.
- To determine the safety profile of rivastigmine in a cohort of long-lasting, aviremic HIV+ patients.
Main Methods:
- A randomized, double-blind, placebo-controlled, crossover study involving 17 aviremic HIV+ patients with HAND.
- Patients received oral rivastigmine (up to 12 mg/day) for 20 weeks, followed by placebo, or vice versa.
- Efficacy was measured using the Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog) and individual neuropsychological tests. Safety was monitored through adverse events and laboratory tests.
Main Results:
- Rivastigmine did not significantly improve ADAS-Cog scores, the primary outcome.
- A significant improvement was observed in processing speed (Trail Making Test A) with rivastigmine treatment (p = 0.03).
- No other significant cognitive improvements were noted, although one measure of executive functioning approached significance (p = 0.069). Adverse events were frequent but comparable to other rivastigmine studies, with no safety concerns.
Conclusions:
- Oral rivastigmine demonstrated a potential benefit in improving psychomotor speed in aviremic HIV+ patients with HAND.
- The drug was not effective in improving overall cognitive function as measured by ADAS-Cog.
- Further investigation using the more tolerable transdermal formulation of rivastigmine is recommended for HAND treatment.
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