18 research outputs found

    Summary of resistance results obtained by all methodologies.<sup>a</sup>

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    a<p>Plasma samples underwent testing by Sanger sequencing (SS), allele-specific PCR (AS-PCR) and ultra-deep sequencing (UDS) targeting mutations in HIV-1 reverse transcriptase.</p

    Factors associated with cause-specific hazard of initial virologic response and virologic failure after cART initiation.

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    1<p>: men having sex with men;<sup> 2</sup>: injecting drug users;<sup> 3</sup>: sex between men and women. Each factor is adjusted for all other factors in Table.</p>*<p>global Wald-type tests based on the fit of the corresponding models.</p

    Predictors of virologic suppression <400 copies/ml 4–12 months after restarting NNRTI-based ART.<sup>a</sup>

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    a<p>The analysis included 90 patients who restarted NNRTI-based ART without a protease inhibitor and had at least one viral load measurement in the 4–12 months after re-starting therapy.</p>b<p>As noted above some patients had the viral load measured by assays with a lower limit of quantification of either 75 or 400 copies/ml. NNRTI = non-nucleoside reverse transcriptase inhibitor; ART = antiretroviral therapy; OR = Odds ratio; CI = confidence interval.</p

    Estimated median (95% CI) CD4 cell count by HIV-1 subtype and time since cART initiation.

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    <p>(Non acute infection, without AIDS at cART initiation, boosted PI cART, seroconversion to cART >4 years, previously naïve, ≥5 log<sub>10</sub> c/ml initial viral load, men having sex with men, 30 years old at cART initiation).</p

    Estimates from fitting a univariate (unadjusted) and a multivariable (adjusted) linear mixed model on all repeated measurements of CD4 cell counts (square root transformed) taken from seroconversion to end of follow-up, cART initiation or clinical AIDS onset.

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    *<p>Baseline category;</p>1<p>: Coefficients denote either mean estimated value for the reference category or mean estimated differences relative to the baseline category;</p>2<p>: Men of non-African origin in European cohorts;</p>3<p>: Individuals of non-African origin in European cohorts, aged 15–29 years at seroconversion and with a ≤6 months gap between seroconversion and study entry.</p

    Characteristics of the study population that interrupted NNRTI-based ART in SMART, according to the interruption modality.<sup>a</sup>

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    a<p>Patients interrupted ART by simultaneously interrupting all drugs, continuing the nucleos(t)ide reverse transcriptase inhibitors (NRTIs) for a short period, or switching to a ritonavir-boosted protease inhibitor for a short period, referred to as simultaneous, staggered and switched interruption respectively.</p>b<p>In 46 patients the viral load was measured by assays with a lower limit of quantification of either 75 or 400 copies/ml and results were “undetectable” below these cut-offs; 19 patients showed a viral load between 50 and 400 copies/ml. NNRTI = non-nucleoside reverse transcriptase inhibitor; ART = antiretroviral therapy; MSM = Men who have sex with men; IQR = interquartile range.</p

    Observed (A) and predicted (B) CD4 cell count by HIV-1 subtype.

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    <p>A: Median profiles (numbers on top indicate individuals contributing measurements at each time point), B: based on a piecewise linear mixed model (Non acute infection, without AIDS at cART initiation, boosted PI cART, SC to cART>4 years, previously naĂŻve, 5 log<sub>10</sub> c/ml initial viral load, men having sex with men, 30 years old at cART initiation).</p
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