4.7 Article

HAART and Progression to High-Grade Anal Intraepithelial Neoplasia in Men Who Have Sex with Men and Are Infected with HIV

Journal

CLINICAL INFECTIOUS DISEASES
Volume 52, Issue 9, Pages 1174-1181

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/cir064

Keywords

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Funding

  1. Reseau FRSQ-SIDA Maladies Infectieuses
  2. Canadian Cancer Society
  3. National Cancer Institute of Canada
  4. Canadian Institutes of Health Research
  5. Canadian HIV Trials Network
  6. Fonds de la Recherche en Sante du Quebec
  7. GlaxoSmithKline
  8. Merck Frosst
  9. Canadian Trial Network
  10. Programme national de mentorat sur le VIH, Symposium VIH annuel
  11. Merck
  12. Roche
  13. Qiagen

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Background. Human immunodeficiency virus (HIV)-seropositive men who have sex with men (MSM) are at risk for anal intraepithelial neoplasia (AIN) and cancer. The goal of this study was to identify risk factors associated with high-grade AIN (AIN-2,3) in HIV-positive MSM, including the receipt of highly active antiretroviral therapy (HAART). Methods. A cohort study involving 247 HIV-seropositive MSM receiving HAART or initiating HAART was followed up every 6 months for 3 years with human papillomavirus (HPV) testing and high-resolution anoscopy to identify predictors of AIN-2,3 by Cox regression analysis and period prevalence logistic regression. Results. AIN-2,3 was observed during the study in 132 (53%) of 247 participants. The progression rate to AIN-2,3 from a lesser abnormality at baseline was 12.8 cases per 1000 person-months (95% confidence interval [CI], 9.8-16.5 cases per 1000 person-months). The risk of AIN-2,3 increased with age (odds ratio [OR], 3.09 [95% CI, 1.12-8.52] for men 40-49 years of age and 4.78 [95% CI, 1.29-17.73] for men >50 years of age, compared with men <40 years of age) and for men whose CD4+ cell counts were <50 cells/mm(3) before starting HAART (OR, 14.40 [95% CI, 1.45-143.58]). Men who had been receiving their current HAART regimen for >4 years had a marginally significant lower risk of AIN-2,3 after adjustment for HPV (OR, 0.28 [95% CI, 0.07-1.06]) compared with those treated for <4 years. Anal HPV type 16 (HPV16) or type 18 (HPV18) infections (OR, 14.18; [95% CI, 3.51-57.32]) and HPV16 and HPV18 co-infection (OR, 31.03 [95% CI, 5.68-169.60]) were strongly associated with progression to AIN-2,3. Conclusion. HPV16 and HPV18 infections and a low nadir CD4+ cell count increase the risk of AIN-2,3. Receiving the same HAART regimen for >4 years may contribute some benefit against AIN-2,3.

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