Key result
Youth HIV infection linked to ~15% higher baseline ICA IMT despite similar 48-week changes.
Why the study?
HIV-infected children and young adults are at increased risk of cardiovascular disease, but longitudinal changes in carotid intima-media thickness and its relationship with cardiovascular risk factors are not well characterized.
Does HIV infection and its treatment affect longitudinal changes in carotid intima-media thickness in children and young adults compared to healthy controls?
Observational (n=72)
Does HIV infection and its treatment affect longitudinal changes in carotid intima-media thickness in children and young adults compared to healthy controls?
Absolute Event Rate: 0.9% vs 0.78%
p-value: p=0.01
HIV-infected children and young adults have higher baseline cIMT than healthy controls, but continuous antiretroviral therapy and lipid control may improve cIMT over time.
OBJECTIVES: HIV-infected patients are at increased risk of cardiovascular disease (CVD). This study assessed longitudinal changes in carotid intima-media thickness (cIMT) as a surrogate marker for CVD, and determined the relationship between cIMT and cardiovascular risk factors in HIV infected children/young adults. METHODS: This was a longitudinal, observational study comparing cIMT,fasting metabolic profile, and C-reactive protein in HIV-infected subjects 2 to 21 years old to matched controls at baseline and 48 weeks. RESULTS: Thirty-five HIV + subjects and 37 controls were included in the analysis. Among HIV + subjects, the median age was 10 years, body mass index was 18.7 kg/m2, 37% were male, CD4 count was 32%, 77% had HIV-RNA 400 copies/mL, and 86% were on antiretrovirals. At baseline,HIV + had higher lipids and C-reactive protein. HIV-infected had higher internal carotid artery (ICA) and common carotid artery (CCA) IMT (mm)(ICA: HIV + , 0.90; controls, 0.78 [P = 0.01]; CCA: HIV + , 1.00; controls,0.95 [P = 0.05]). At 48 weeks, CD4% increased and low-density lipoprotein decreased in HIV-infected subjects. ICA and CCA median changes for HIV-infected subjects were -0.23 and -0.15 mm, respectively (both P 0.01). In controls, only CCA changed (P = 0.04). Between-group changes were not significant, except when only 31 perinatally infected HIV - subjects and the controls were compared (CCA P = 0.04). In multiple regression analyses of HIV + subjects, antiretroviral therapy duration and CD4% were associated with cIMT changes. CONCLUSIONS: Higher cIMT was found in HIV-infected subjects than in healthy controls, but at 48 weeks, cIMT was similar between groups. These data suggest that HIV-infected children/young adults are at high risk of CVD, but lipid control, immune restoration, and viral suppression with continuous antiretroviral therapy may prevent its worsening.
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Ross et al. (2010) conducted an observational in HIV infection (n=72). HIV infection vs. Healthy controls was evaluated on Baseline internal carotid artery (ICA) intima-media thickness (IMT) (p=0.01). HIV infection in children and young adults was associated with higher baseline internal carotid artery IMT compared to controls (0.90 vs 0.78 mm; P=0.01), though 48-week changes were similar.
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