Can high central nervous system penetrating antiretroviral regimens protect against the onset of HIV-associated neurocognitive disorders?

2014 
Objective: Toassess changesovertime inneuropsychologicaltest results(NPr) andrisk factors among a regularly followed HIV-infected patient population. Methods: Prospective cohort of HIV-infected patients randomly selected to undergo neuropsychological follow-up. Test score was adjusted for age, sex and education. Patients were divided into five groups: normal tests, neuropsychological deficit (one impaired cognitive domain), asymptomatic neurocognitive disorders (ANIs), mild neurocognitive disorders (MNDs) and HIV-associated dementia (HAD). Demographic andbackgroundparametersincludingCSFdrugconcentrationpenetrationeffectiveness (CPE) score 2010 were recorded. Changes in NPr and associated risk factors were analyzed. Results: Two hundred and fifty-six patients underwent neuropsychological tests and 96accepted follow-up approximately 2 years later. The groups were comparable. Upon neuropsychological retesting, six patients improved, 31 worsened and 59 were stable. The proportion of patients with HIV-associated neurocognitive disorders (HANDs) rose from 26 to 45%, with ANIs and MNDs still mostly represented. Most patients initially diagnosed with HANDs remained stable, five of 25 showed clinical improvement and three of 25 deteriorated. Of 33 patients with normal tests, four deteriorated, whereas 24of 38 with initial neuropsychologicaldeficit had poorer NPr, and contributed most of the new HAND cases. Patients with clinical deterioration had a lower CPE score both at inclusion (6.9 vs. 8.1; P ¼0.005) and at the end of follow-up (7.2 vs. 7.8; P ¼0.08) than those with improved or stable performance. This was confirmed by multivariate analysis. Conclusion: Patients with higher CPE scores upon inclusion and at the end of follow-up were at lower risk of clinical worsening, suggesting that combination antiretroviral therapy with better CSF penetration could protect against cognitive deterioration. 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins AIDS 2014, 28:493‐501
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