4.1 Article

Does gender or mode of HIV acquisition affect virological response to modern antiretroviral therapy (ART)?

期刊

HIV MEDICINE
卷 17, 期 1, 页码 18-27

出版社

WILEY
DOI: 10.1111/hiv.12272

关键词

antiretroviral therapy; gender inequality; HIV; HIV acquisition; men who have sex with men; men who have sex with women; treatment outcomes; virological control

资金

  1. British Infection Association
  2. Highly Active Antiretroviral Therapy Oversight Committee (HAART-OC)
  3. European Agency for the Evaluation of Medicinal Products
  4. United States Food and Drug Administration
  5. European Union
  6. Abbott Laboratories
  7. Boehringer Ingelheim Pharmaceuticals Inc.
  8. Bristol-Myers Squibb
  9. Gilead Sciences Inc.
  10. Viiv Healthcare
  11. Merck Co Inc.
  12. Pfizer Inc
  13. F. Hoffman-LaRoche Ltd
  14. Janssen Pharmaceuticals

向作者/读者索取更多资源

Objectives Previous UK studies have reported disparities in HIV treatment outcomes for women. We investigated whether these differences persist in the modern antiretroviral treatment (ART) era. Methods A single-centre cohort analysis was carried out. We included in the study all previously ART-naive individuals at our clinic starting triple ART from 1 January 2006 onwards with at least one follow-up viral load (VL). Time to viral suppression (VS; first viral load < 50 HIV-1 RNA copies/mL), virological failure (VF; first of two consecutive VLs > 200 copies/mL more than 6 months post-ART) and treatment modification were estimated using standard survival methods. Results Of 1086 individuals, 563 (52%) were men whose risk for HIV acquisition was sex with other men (MSM), 207 (19%) were men whose risk for HIV acquisition was sex with women (MSW) and 316 (29%) were women. Median pre-ART CD4 count and time since HIV diagnosis in these groups were 298, 215 and 219 cells/mu L, and 2.3, 0.3 and 0.3 years, respectively. Time to VS was comparable between groups, but women [adjusted hazard ratio (aHR) 2.32; 95% confidence interval (CI) 1.28-4.22] and MSW (aHR 3.28; 95% CI 1.91-5.64) were at considerably higher risk of VF than MSM. Treatment switches and complete discontinuation were also more common among MSW [aHR 1.38 (95% CI 1.04-1.81) and aHR 1.73 (95% CI 0.97-3.16), respectively] and women [aHR 1.87 (95% CI 1.43-2.46) and aHR 3.20 (95% CI 2.03-5.03), respectively] than MSM. Conclusions Although response rates were good in all groups, poorer virological outcomes for women and MSW have persisted into the modern ART era. Factors that might influence the differences include socioeconomic status and mental health disorders. Further interventions to ensure excellent response rates in women and MSW are required.

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