TY - JOUR
T1 - Rate of CD4+ cell count increase over periods of viral load suppression: relationship with the number of previous virological failures.
AU - Trotta, Mp
AU - Cozzi Lepri, Alessandro
AU - Ammassari, Adriana
AU - Vecchiet, J
AU - Cassola, G
AU - Caramello, P
AU - Vullo, Vincenzo
AU - Soscia, F
AU - Chiodera, A
AU - Ladisa, N
AU - Abeli, C
AU - Cauda, Roberto
PY - 2010
Y1 - 2010
N2 - Background. Although the kinetics of CD4+ cell counts have been extensively studied in antiretroviral-naive HIV-infected patients, data on individuals who have failed combination antiretroviral therapy (cART) are lacking.
Methods. This analysis was based on the ICONA Foundation Study. Subjects with ≥1 episode of viral suppression after starting first-line cART were included (n = 3537). Following a viral rebound, patients who achieved another episode of viral suppression could reenter the analysis. The percentage of patients with an increase in CD4+ cell count >300 cells/mm3 was estimated using Kaplan-Meier techniques; the rate of CD4+ cell count increase per year was estimated using a multivariable, multilevel linear model with fixed effects of intercept and slope. Multivariable models were also fitted to include several covariates.
Results. The median time to reach a CD4+ cell count increase >300 cells/mm3 from baseline was significantly associated with the number of failed regimens: 34 months, 41 months, 51 months, and 45 months in subjects without evidence of previous virological failure, or 1, 2, or ≥3 previous virologically failed regimens, respectively (P < .001, by log-rank test). The annual estimated increases in CD4+ cell count were 36 cells/mm3 (95% confidence interval [CI], 34 38 cells/mm3), 28 cells/mm3 (95% CI, 11 21 cells/mm3), 31 cells/mm3 (95% CI, 26 36 cells/ mm3), and 26 cells/mm3 (95% CI, 18 33 cells/mm3), respectively. Differences in the annual CD4+ cell count increase were observed between specific antiretrovirals.
Conclusions. Subjects with ≥1 virological failure took a longer time to reach a CD4+ cell count >300 cell/ mm3 and had a slower annual increase than those without virological failure. Efforts should be made to optimize first-line cART, because this represents the best chance of achieving an effective CD4(+) response.
AB - Background. Although the kinetics of CD4+ cell counts have been extensively studied in antiretroviral-naive HIV-infected patients, data on individuals who have failed combination antiretroviral therapy (cART) are lacking.
Methods. This analysis was based on the ICONA Foundation Study. Subjects with ≥1 episode of viral suppression after starting first-line cART were included (n = 3537). Following a viral rebound, patients who achieved another episode of viral suppression could reenter the analysis. The percentage of patients with an increase in CD4+ cell count >300 cells/mm3 was estimated using Kaplan-Meier techniques; the rate of CD4+ cell count increase per year was estimated using a multivariable, multilevel linear model with fixed effects of intercept and slope. Multivariable models were also fitted to include several covariates.
Results. The median time to reach a CD4+ cell count increase >300 cells/mm3 from baseline was significantly associated with the number of failed regimens: 34 months, 41 months, 51 months, and 45 months in subjects without evidence of previous virological failure, or 1, 2, or ≥3 previous virologically failed regimens, respectively (P < .001, by log-rank test). The annual estimated increases in CD4+ cell count were 36 cells/mm3 (95% confidence interval [CI], 34 38 cells/mm3), 28 cells/mm3 (95% CI, 11 21 cells/mm3), 31 cells/mm3 (95% CI, 26 36 cells/ mm3), and 26 cells/mm3 (95% CI, 18 33 cells/mm3), respectively. Differences in the annual CD4+ cell count increase were observed between specific antiretrovirals.
Conclusions. Subjects with ≥1 virological failure took a longer time to reach a CD4+ cell count >300 cell/ mm3 and had a slower annual increase than those without virological failure. Efforts should be made to optimize first-line cART, because this represents the best chance of achieving an effective CD4(+) response.
KW - HIV
KW - Viral load
KW - Virological Failure
KW - HIV
KW - Viral load
KW - Virological Failure
UR - http://hdl.handle.net/10807/6364
M3 - Article
SN - 1058-4838
VL - 2010
SP - 456
EP - 464
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
ER -