TY - JOUR
T1 - Evaluation of viral load thresholds for predicting new World Health Organization stage 3 and 4 events in HIV-infected children receiving highly active antiretroviral therapy
AU - for the NISDI PLACES Protocol
AU - Siberry, George K.
AU - Harris, D. Robert
AU - Oliveira, Ricardo Hugo
AU - Krauss, Margot R.
AU - Hofer, Cristina B.
AU - Tiraboschi, Adriana Aparecida
AU - Marques, Heloisa
AU - Succi, Regina C.
AU - Abreu, Thalita
AU - Negra, Marinella Della
AU - Mofenson, Lynne M.
AU - Hazra, Rohan
PY - 2012/6/1
Y1 - 2012/6/1
N2 - Background: This study evaluated a wide range of viral load (VL) thresholds to identify a cut-point that best predicts new clinical events in children on stable highly active antiretroviral therapy (HAART). Methods: Cox proportional hazards modeling was used to assess the adjusted risk for World Health Organization stage 3 or 4 clinical events (WHO events) as a function of time-varying CD4, VL, and hemoglobin values in a cohort study of Latin American children on HAART ≥6 months. Models were fit using different VL cut-points between 400 and 50,000 copies per milliliter, with model fit evaluated on the basis of the minimum Akaike information criterion value, a standard model fit statistic. Results: Models were based on 67 subjects with WHO events out of 550 subjects on study. The VL cut-points of >2600 and >32,000 copies per milliliter corresponded to the lowest Akaike information criterion values and were associated with the highest hazard ratios (2.0, P = 0.015; and 2.1, P = 0.0058, respectively) for WHO events. Conclusions: In HIV-infected Latin American children on stable HAART, 2 distinct VL thresholds (>2600 and >32,000 copies/mL) were identified for predicting children at significantly increased risk for HIV-related clinical illness, after accounting for CD4 level, hemoglobin level, and other significant factors.
AB - Background: This study evaluated a wide range of viral load (VL) thresholds to identify a cut-point that best predicts new clinical events in children on stable highly active antiretroviral therapy (HAART). Methods: Cox proportional hazards modeling was used to assess the adjusted risk for World Health Organization stage 3 or 4 clinical events (WHO events) as a function of time-varying CD4, VL, and hemoglobin values in a cohort study of Latin American children on HAART ≥6 months. Models were fit using different VL cut-points between 400 and 50,000 copies per milliliter, with model fit evaluated on the basis of the minimum Akaike information criterion value, a standard model fit statistic. Results: Models were based on 67 subjects with WHO events out of 550 subjects on study. The VL cut-points of >2600 and >32,000 copies per milliliter corresponded to the lowest Akaike information criterion values and were associated with the highest hazard ratios (2.0, P = 0.015; and 2.1, P = 0.0058, respectively) for WHO events. Conclusions: In HIV-infected Latin American children on stable HAART, 2 distinct VL thresholds (>2600 and >32,000 copies/mL) were identified for predicting children at significantly increased risk for HIV-related clinical illness, after accounting for CD4 level, hemoglobin level, and other significant factors.
KW - Latin America
KW - Pediatric HIV infection
KW - Viral load monitoring
KW - Viral load threshold
UR - http://www.scopus.com/inward/record.url?scp=84862137424&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84862137424&partnerID=8YFLogxK
U2 - 10.1097/QAI.0b013e31824e4da6
DO - 10.1097/QAI.0b013e31824e4da6
M3 - Article
C2 - 22343177
AN - SCOPUS:84862137424
SN - 1525-4135
VL - 60
SP - 214
EP - 218
JO - Journal of Acquired Immune Deficiency Syndromes
JF - Journal of Acquired Immune Deficiency Syndromes
IS - 2
ER -