Key result
In Ugandan youth with perinatally acquired HIV, common carotid artery IMT decreased and PWV increased over 96 weeks (P≤0.03), whereas IMT increased in uninfected controls (P=0.03).
Why the study?
Prospective investigations evaluating the risk of cardiovascular disease among youth with perinatally acquired HIV in sub-Saharan Africa are lacking.
Does perinatally acquired HIV on ART affect subclinical vascular disease progression (IMT and PWV) in youth compared to HIV-uninfected controls?
Cohort (n=198)
No
Does perinatally acquired HIV on ART affect subclinical vascular disease progression (IMT and PWV) in youth compared to HIV-uninfected controls?
p-value: p=≤.03
ART duration was associated with lower PWV in Ugandan youth with perinatally acquired HIV; hypothesis-generating and should not yet change practice.
BACKGROUND: Prospective investigations on the risk of cardiovascular disease among youth with perinatally acquired human immunodeficiency virus (PHIV) in sub-Saharan Africa are lacking. METHODS: A prospective observational cohort study was performed in 101 youth (aged 10-18 years) with PHIV and 97 who were human immunodeficiency virus (HIV) uninfected (HIV-), from 2017 to 2021 at the Joint Clinical Research Center in Uganda. Participants with PHIV were receiving antiretroviral therapy (ART) and had HIV-1 RNA levels ≤400 copies/mL. The common carotid artery intima-media thickness (IMT) and pulse wave velocity (PWV) were evaluated at baseline and at 96 weeks. Groups were compared using unpaired t-test, and potential predictors of IMT and PWV were assessed using quantile regression. RESULTS: Of the 198 participants recruited at baseline, 168 (89 with PHIV, 79 HIV-) had measurements at 96 weeks. The median age (interquartile range) age was 13 (11-15) years; 52% were female, and 85% had viral loads <50 copies/mL that remained undetectable at week 96. The baseline mean common carotid artery IMT was slightly higher in participants with PHIV compared with controls (P < .01), and PWV did not differ between groups (P = .08). At week 96, IMT decreased and PWV increased in the PHIV group (P ≤ .03); IMT increased in the HIV- group (P = .03), with no change in PWV (P = .92). In longitudinal analyses in those with PHIV, longer ART duration was associated with lower PWV (β = .008 [95% confidence interval, -.008 to .003]), and abacavir use with greater IMT (β = .043 [.012-.074]). CONCLUSIONS: In healthy Ugandan youth with PHIV, virally suppressed by ART, the common carotid artery IMT did not progress over 2 years. Prolonged and early ART may prevent progression of subclinical vascular disease, while prolonged use of abacavir may increase it.
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Dirajlal‐Fargo et al. (2022) conducted a cohort in Perinatally acquired human immunodeficiency virus (PHIV) (n=198). Perinatally acquired human immunodeficiency virus (PHIV) vs. HIV-uninfected youth was evaluated on Change in common carotid artery intima-media thickness (IMT) and pulse wave velocity (PWV) at 96 weeks (p=≤.03). In Ugandan youth with perinatally acquired HIV, common carotid artery IMT decreased and PWV increased over 96 weeks (P≤0.03), whereas IMT increased in uninfected controls (P=0.03).
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