TY - JOUR
T1 - Pretreatment CD4 cell slope and progression to AIDS or death in HIV-infected patients initiating antiretroviral therapy--the CASCADE collaboration: a collaboration of 23 cohort studies
AU - Wolbers, Marcel
AU - Babiker, Abdel
AU - Sabin, Caroline
AU - Young, Jim
AU - Dorrucci, Maria
AU - Chêne, Geneviève
AU - Mussini, Cristina
AU - Porter, Kholoud
AU - Bucher, Heiner C.
AU - AUTHOR GROUP
AU - del Amo, Julia
AU - Meyer, Laurence
AU - Pillay, Deenan
AU - Prins, Maria
AU - Rosinska, Magda
AU - Touloumi, Giota
AU - Lodi, Sara
AU - Coughlin, Kate
AU - Walker, Sarah
AU - Darbyshire, Janet
AU - de Luca, Andrea
AU - Fisher, Martin
AU - Muga, Roberto
AU - Kaldor, John
AU - Kelleher, Tony
AU - Ramacciotti, Tim
AU - Gelgor, Linda
AU - Cooper, David
AU - Smith, Don
AU - Gill, John
AU - Jørgensen, Louise Bruun
AU - Nielsen, Claus
AU - Lutsar, Irja
AU - Dabis, Francois
AU - Thiebaut, Rodolphe
AU - Masquelier, Bernard
AU - Costagliola, Dominique
AU - Guiguet, Marguerite
AU - Vanhems, Philippe
AU - Chaix, Marie-Laure
AU - Ghosn, Jade
AU - Boufassa, Faroudy
AU - Hamouda, Osamah
AU - Kucherer, Claudia
AU - Pantazis, Nikos
AU - Hatzakis, Angelos
AU - Paraskevis, Dimitrios
AU - Karafoulidoua, Anastasia
AU - van der Helm, Jannie
AU - Geskus, Ronald
AU - Schuitemaker, Hanneke
PY - 2010
Y1 - 2010
N2 - BACKGROUND: CD4 cell count is a strong predictor of the subsequent risk of AIDS or death in HIV-infected patients initiating combination antiretroviral therapy (cART). It is not known whether the rate of CD4 cell decline prior to therapy is related to prognosis and should, therefore, influence the decision on when to initiate cART. METHODS AND FINDINGS: We carried out survival analyses of patients from the 23 cohorts of the CASCADE (Concerted Action on SeroConversion to AIDS and Death in Europe) collaboration with a known date of HIV seroconversion and with at least two CD4 measurements prior to initiating cART. For each patient, a pre-cART CD4 slope was estimated using a linear mixed effects model. Our primary outcome was time from initiating cART to a first new AIDS event or death. We included 2,820 treatment-naïve patients initiating cART with a median (interquartile range) pre-cART CD4 cell decline of 61 (46-81) cells/microl per year; 255 patients subsequently experienced a new AIDS event or death and 125 patients died. In an analysis adjusted for established risk factors, the hazard ratio for AIDS or death was 1.01 (95% confidence interval 0.97-1.04) for each 10 cells/microl per year reduction in pre-cART CD4 cell decline. There was also no association between pre-cART CD4 cell slope and survival. Alternative estimates of CD4 cell slope gave similar results. In 1,731 AIDS-free patients with >350 CD4 cells/microl from the pre-cART era, the rate of CD4 cell decline was also not significantly associated with progression to AIDS or death (hazard ratio 0.99, 95% confidence interval 0.94-1.03, for each 10 cells/microl per year reduction in CD4 cell decline). CONCLUSIONS: The CD4 cell slope does not improve the prediction of clinical outcome in patients with a CD4 cell count above 350 cells/microl. Knowledge of the current CD4 cell count is sufficient when deciding whether to initiate cART in asymptomatic patients. Please see later in the article for the Editors' Summary
AB - BACKGROUND: CD4 cell count is a strong predictor of the subsequent risk of AIDS or death in HIV-infected patients initiating combination antiretroviral therapy (cART). It is not known whether the rate of CD4 cell decline prior to therapy is related to prognosis and should, therefore, influence the decision on when to initiate cART. METHODS AND FINDINGS: We carried out survival analyses of patients from the 23 cohorts of the CASCADE (Concerted Action on SeroConversion to AIDS and Death in Europe) collaboration with a known date of HIV seroconversion and with at least two CD4 measurements prior to initiating cART. For each patient, a pre-cART CD4 slope was estimated using a linear mixed effects model. Our primary outcome was time from initiating cART to a first new AIDS event or death. We included 2,820 treatment-naïve patients initiating cART with a median (interquartile range) pre-cART CD4 cell decline of 61 (46-81) cells/microl per year; 255 patients subsequently experienced a new AIDS event or death and 125 patients died. In an analysis adjusted for established risk factors, the hazard ratio for AIDS or death was 1.01 (95% confidence interval 0.97-1.04) for each 10 cells/microl per year reduction in pre-cART CD4 cell decline. There was also no association between pre-cART CD4 cell slope and survival. Alternative estimates of CD4 cell slope gave similar results. In 1,731 AIDS-free patients with >350 CD4 cells/microl from the pre-cART era, the rate of CD4 cell decline was also not significantly associated with progression to AIDS or death (hazard ratio 0.99, 95% confidence interval 0.94-1.03, for each 10 cells/microl per year reduction in CD4 cell decline). CONCLUSIONS: The CD4 cell slope does not improve the prediction of clinical outcome in patients with a CD4 cell count above 350 cells/microl. Knowledge of the current CD4 cell count is sufficient when deciding whether to initiate cART in asymptomatic patients. Please see later in the article for the Editors' Summary
U2 - 10.1371/journal.pmed.1000239
DO - 10.1371/journal.pmed.1000239
M3 - Article
C2 - 20186270
SN - 1549-1277
VL - 7
SP - e1000239
JO - PLoS medicine
JF - PLoS medicine
IS - 2
ER -