Arterial stiffness and endothelial dysfunction in HIV-infected children

The role of antiretroviral therapy in acceleration of atherosclerosis in HIV-infected adults is controversial, partly because of the confounding effects of the involvement of classic cardiovascular risk factors. To study vascular function in HIV-infected children. Cross-sectional study of 49 HIV-inf...

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Veröffentlicht in:AIDS (London) 2004-04, Vol.18 (7), p.1037-1041
Hauptverfasser: BONNET, Damien, AGGOUN, Yacine, SZEZEPANSKI, Isabelle, BELLAL, Nassima, BLANCHE, Stéphane
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Sprache:eng
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Zusammenfassung:The role of antiretroviral therapy in acceleration of atherosclerosis in HIV-infected adults is controversial, partly because of the confounding effects of the involvement of classic cardiovascular risk factors. To study vascular function in HIV-infected children. Cross-sectional study of 49 HIV-infected children (34 receiving antiretroviral therapy and 15 never treated) and if 24 age- and sex-matched controls. Automatic, computerized, ultrasonic procedure evaluation of geometric and mechanical properties of the common carotid artery, and of the endothelium-dependent dilation and endothelium-independent dilation. Relative systolodiastolic variations in diameter of the carotid artery in HIV-infected children were significantly lower than those in controls, but there was no significant difference in intima-media thickness. Cross-sectional compliance and distensibility were also significantly lower. Wall stiffness, assessed as the incremental elastic modulus, was larger in HIV-infected children. Endothelium-dependent dilation was lower in HIV-infected children but non-endothelium-dependent dilation was similar to that in controls. We did not find differences for any of the vascular variables between HIV-infected children receiving antiretroviral therapy and those never treated. All arterial variables were similar in children with and without dyslipidemia. HIV-infected children had a vascular dysfunction in the absence of cardiovascular risk factors. In this short series, no additional detrimental effects were observed after a mean of 5 years of antiretroviral therapy.
ISSN:0269-9370
1473-5571
DOI:10.1097/00002030-200404300-00012