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Longitudinal Evaluation of Hyperlipidemia in HIV-infected Children Starting their First Line HAART Regimen
José Tomás Ramos*1, S Guillén1, M Martínez1, R Resino2, J Bellón2, J Beceiro3, C Calvo4, M De José5, M Gurbindo2, J Martínez6, and Cohorte de Madrid
1Hosp 12 de Octubre, Madrid, Spain; 2Hosp Gen Univ Gregorio Marañón, Madrid, Spain; 3Hosp Alcala de Henares, Spain; 4Hosp de Leganés, Spain; 5Hosp La Paz, Spain; and 6Hosp del Niño Jesús, Spain
Background: Lipid disorders are very common in HIV-infected children treated with
HAART. Nevertheless, there are few longitudinal studies on this issue in
children. Objectives: To assess the effect of HAART on cholesterol and
triglycerides plasma levels, and the possible contribution of each individual
antiretroviral.
Patients
and methods: Children included in the study were
selected out from the Madrid cohort study, a large cohort of HIV-infected
children. Only children starting 2 NRTI plus either a PI or a NNRTI were
included, provided they had baseline cholesterol and triglycerides available
before HAART, and serial assessment for at least 12 months with their first
HAART regimen. Comparison were made among each individual antiretroviral.
Results: In 122 children with baseline lipid levels, the first HAART regimen
was started and maintained for at least 12 months since 1997. Median age at the
initiation of HAART was 6.2 years (1 month-18 years). 39% were antiretroviral
naïve, and 61% had prior mono or dual NRTI therapy. Among the PIs, nelfinavir
was used in 46, ritonavir in 16, indinavir in 23, saquinavir in 10 and
lopinavir/r in 4 children. Among the NNRTI, 16 children started efavirenz and 7
nevirapine. At baseline 7% and 12% of children treated with PI had cholesterol
and triglycerides greater than 200 mg/dl and 170 mg/dl, respectively. At 12
months, cholesterol and triglycerides raised above these values in 41%
(p<0.01) and 17%(p: 0.4). These proportions in cholesterolemia were 67%,
40%, 20%, 50%, and 67% for ritonavir, nelfinavir, indinavir, saquinavir, and
lopinavir/r, respectively. Median increases at 12 months were 74 mg/dl for
ritonavir, 38 mg/dl for nelfinavir, 17 mg/dl for indinavir, 19 mg/dl for
saquinavir, and 29 mg/dl for lopinavir/r, whereas no significant changes were
observed over time in triglyceridemia. In comparative analysis at 12 months,
ritonavir resulted in significantly higher increases in cholesterol than
nelfinavir, indinavir and saquinavir (p<0.05). NNRTI were not associated with
significant increases in either cholesterol or triglycerides.
Conclusions: HIV-infected children experienced significant increases in
cholesterolemia with most PI-containing-regimens. Ritonavir is associated with
the greatest raise in plasma cholesterol in the first year of HAART.
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