4.7 Article

Antiretroviral therapy CNS penetration and HIV-1-associated CNS disease

Journal

NEUROLOGY
Volume 76, Issue 8, Pages 693-700

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e31820d8b0b

Keywords

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Funding

  1. Abbott
  2. Boehringer Ingelheim
  3. Gilead Sciences, Inc.
  4. Tibotec Therapeutics
  5. Janssen
  6. Pfizer Inc.
  7. TRXCare Ltd
  8. NHS Westminster
  9. GlaxoSmithKline/ViiV Healthcare
  10. Bristol-Myers Squibb
  11. Merck Serono
  12. Roche
  13. ViiV Healthcare
  14. GlaxoSmithKline
  15. Astellas Pharma Inc.
  16. Medical Research Council (MRC)
  17. British HIV Association
  18. UK Department of Health
  19. NIHR
  20. Wellcome Trust
  21. Cancer Research UK
  22. Medical Research Council, UK [G0000199, G0600337]
  23. MRC [MC_U122886351, G0900274, G0600337] Funding Source: UKRI
  24. Medical Research Council [G0600337, G0900274, MC_U122886351] Funding Source: researchfish

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Objective: The impact of different antiretroviral agents on the risk of developing or surviving CNS disease remains unknown. The aim of this study was to investigate whether using antiretroviral regimens with higher CNS penetration effectiveness (CPE) scores was associated with reduced incidence of CNS disease and improved survival in the UK Collaborative HIV Cohort (CHIC) Study. Methods: Adults without previous CNS disease, who commenced combination antiretroviral therapy (cART) between 1996 and 2008, were included (n = 22,356). Initial and most recent cART CPE scores were calculated. CNS diseases were HIV encephalopathy (HIVe), progressive multifocal leukoencephalopathy (PML), cerebral toxoplasmosis (TOXO), and cryptococcal meningitis (CRYPTO). Incidence rates and overall survival were stratified by CPE score. A multivariable Poisson regression model was used to identify independent associations. Results: The median (interquartile range) CPE score for initial cART regimen increased from 7 (5-8) in 1996-1997 to 9 (8-10) in 2000-2001 and subsequently declined to 6 (7-8) in 2006-2008. Differences in gender, HIV acquisition risk group, and ethnicity existed between CPE score strata. A total of 251 subjects were diagnosed with a CNS disease (HIVe 80; TOXO 59; CRYPTO 56; PML 54). CNS diseases occurred more frequently in subjects prescribed regimens with CPE scores <= 4, and less frequently in those with scores >= 10; however, these differences were nonsignificant. Initial and most recent cART CPE scores <= 4 were independently associated with increased risk of death. Conclusion: Clinical status at time of commencing cART influences antiretroviral selection and CPE score. This information should be considered when utilizing CPE scores for retrospective analyses. Neurology (R) 2011; 76:693-700

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