PT - JOURNAL ARTICLE AU - Simioni, Samanta AU - Cavassini, Matthias AU - Annoni, Jean-Marie AU - Métral, Mélanie AU - Iglesias, Katia AU - Rimbault Abraham, Aline AU - Jilek, Samantha AU - Calmy, Alexandra AU - Müller, Hubertus AU - Fayet-Mello, Aurélie AU - Giacobini, Ezio AU - Hirschel, Bernard AU - Du Pasquier, Renaud A. TI - Rivastigmine for HIV-associated neurocognitive disorders AID - 10.1212/WNL.0b013e3182815497 DP - 2013 Feb 05 TA - Neurology PG - 553--560 VI - 80 IP - 6 4099 - http://n.neurology.org/content/80/6/553.short 4100 - http://n.neurology.org/content/80/6/553.full SO - Neurology2013 Feb 05; 80 AB - Objective: To assess the efficacy and safety of rivastigmine for the treatment of HIV-associated neurocognitive disorders (HAND) in a cohort of long-lasting aviremic HIV+ patients.Methods: Seventeen aviremic HIV+ patients with HAND were enrolled in a randomized, double-blind, placebo-controlled, crossover study to receive either oral rivastigmine (up to 12 mg/day for 20 weeks) followed by placebo (20 weeks) or placebo followed by rivastigmine. Efficacy endpoints were improvement on rivastigmine in the Alzheimer's Disease Assessment Scale–Cognitive subscale (ADAS-Cog) and individual neuropsychological scores of information processing speed, attention/working memory, executive functioning, and motor skills. Measures of safety included frequency and nature of adverse events and abnormalities on laboratory tests and on plasma concentrations of antiretroviral drugs. Analyses of variance with repeated measures were computed to look for treatment effects.Results: There was no change on the primary outcome ADAS-Cog on drug. For secondary outcomes, processing speed improved on rivastigmine (Trail Making Test A: F1,13 = 5.57, p = 0.03). One measure of executive functioning just failed to reach significance (CANTAB Spatial Working Memory [strategy]: F1,13 = 3.94, p = 0.069). No other change was observed. Adverse events were frequent, but not different from those observed in other populations treated with rivastigmine. No safety issues were recorded.Conclusions: Rivastigmine in aviremic HIV+ patients with HAND seemed to improve psychomotor speed. A larger trial with the better tolerated transdermal form of rivastigmine is warranted.Classification of evidence: This study provides Class III evidence that rivastigmine is ineffective for improving ADAS-Cog scores, but is effective in improving some secondary outcome measures in aviremic HIV+ patients with HAND.AD=Alzheimer disease; ADAS-Cog=Alzheimer's Disease Assessment Scale–Cognitive subscale; CANTAB=Cambridge Neuropsychological Test Automated Battery; cART=combined antiretroviral therapy; ChEI=cholinesterase inhibitors; DSM-IV=Diagnostic and Statistical Manual of Mental Disorders, 4th edition; HAD=HIV-associated dementia; HAD-A=Hospital Anxiety and Depression scale–anxiety; HAD-D=Hospital Anxiety and Depression scale–depression; HAND=HIV-associated neurocognitive disorders; HDS=HIV Dementia Scale; LP=lumbar puncture; MND=mild neurocognitive disorders; MOS-HIV=Medical Outcome Study HIV Health Survey; NNRTI=non-nucleoside reverse transcriptase inhibitors; PD=Parkinson disease; QoL=quality of life; SWM=Spatial Working Memory; TDM=therapeutic drug monitoring; TMT=Trail Making Test