4.4 Article

Sex differences in the clinical, immunological and virological parameters of HIV-infected patients treated with HAART

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AIDS
卷 21, 期 7, 页码 835-843

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0b013e3280b0774a

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CD34 cell counts; viral load; antiretroviral therapy; gender differences; outcome

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Objective: To compare the clinical, virological and immunological parameters of men and women at baseline and during antiretroviral treatment. Methods: Analysis over time of data collected prospectively from of 2620 patients in a large cohort of HIV-infected patients followed for 12 months after initiating a nelfinavir-based antiretroviral regimen. Results: Women had higher CD4 cell counts (P < 0.001), lower viral load (P < 0.001) and more favourable clinical profile (P < 0.001) than men at baseline. Following treatment, antiretroviral drug-naive women had higher CD4 cell count (P = 0.01) over time than drug-naive men but similar virological responses (P = 0.6); among drug-experienced individuals, women had also better immunological (P = 0.06) and similar virological (P = 0.3) responses compared with men. Consequently, the viroim-munological profile was significantly more favourable in women at each time point. The rates of clinical progression or death were also lower in women (P = 0.008), although drug toxicity was observed more commonly in women (P = 0.09). The highest viroimmunological responses were observed during the first 3 months of therapy in both sexes, although virological responses were achieved up to the 6th month in drug-naive patients. Sex was significantly associated with clinical (P = 0.01), virological (P = 0.01) and immunological (P = 0.006) responses to antiretroviral treatment in multivariate analyses after adjustment for other variables. The differences between genders were not explained by different adherence to therapy. Conclusions: Women have more favourable clinical and viroimmunological patterns than men both at baseline and during antiretroviral treatment. Sex has a small but significant influence on the clinical and laboratory outcomes of HIV infection. (c) 2007 Lippincott Williams & Wilkins.

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