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Risk of progression to AIDS and death in women infected with HIV-1 initiating highly active antiretroviral treatment at different stages of disease

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ARCHIVES OF INTERNAL MEDICINE
卷 162, 期 17, 页码 1973-1980

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AMER MEDICAL ASSOC
DOI: 10.1001/archinte.162.17.1973

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  1. NIAID NIH HHS [U01-AI-34989, U01-AI-34994, U01-AI35004, U01-AI-34993, N01-AI-35161, U01-AI-42590, U01-AI31834] Funding Source: Medline
  2. NICHD NIH HHS [U01-HD-32632] Funding Source: Medline

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Background: The optimal virologic and immunologic stage at which to initiate antiretroviral therapy in individuals infected with human immunodeficiency virus type 1 (HIV-1) is undefined. Methods: Among 1054 HIV-1-infected women in a prospective cohort study, we determined the time from initiation of highly active antiretroviral treatment (HAART) to acquired immunodeficiency syndrome (AIDS) and death. Results: Median follow-up was 3.4 years. Of 553 women without AIDS at HAART initiation, 62 (11%) developed AIDS. Compared with women with CD4(+) cell counts greater than 350/muL at HAART initiation, women with cell counts of 200 to 350/muL and less than 200/muL had relative hazards (RHs) for progression to AIDS of 0.93 (95% confidence interval [CI], 0.46-1.86) and 2.48 (95% CI, 1.39-4.42), respectively. Compared with those with HIV-1 RNA values less than 5000 copies/mL, women with 5000 to 50000 copies/mL and greater than 50000 copies/mL had RHs of 1.39 (95% CI, 0.74-2.64) and 2.09 (95% CI, 1.09-3.99), respectively. Among women with AIDS at HAART initiation (n=501), RHs of death were 1.97 (95% Cl, 0.84-4.66) and 3.35 (95% CI, 1.59-7.08) with CD4(+) cell counts of 200 to 350/muL and less than 200/muL, respectively, relative to those with greater than 350/muL, and 1.90 (95% CI, 0.84-4.30) and 3.70 (95% CI, 1.81-7.54) for those with HIV-1 RNA values of 5000 to 50 000 and greater than 50000 copies/mL, respectively, relative to those with less than 5000 copies/mL. Conclusions: Progression to AIDS and death was predicted by pre-HAART values of less than 200/muL for CD4(+) cells and greater than 50 000 HIV-1 RNA copies/mL, indicating that deferral of HAART until the CD4(+) cell count is between 350 and 200/muL is a valid strategy in the clinical management of HIV-1 infection.

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