This is a substudy of MARCH, in which we are exploring the changes in the vascular endothelium using pulse wave tonometry (a non invasive measure of cardiac health) to measure the changes in small and large arterial elasticity in participants of the MARCH study who switch to maraviroc-based regimens over 96 weeks of follow-up.
Cardiovascular disease is increasingly recognised as a complication of HIV +/- therapies to treat it. Blood vessel elasticity, or compliance, can be depicted as the ability of the vessels to convert intermittent blood flow (cardiac ejection during systole) to continuous blood flow throughout the cardiac cycle. The compliance, or ability of vessels to accept energy, can be subdivided into elasticity of large and small vessels. Pulse wave tonometry is a non-invasive technique performed using a hand-held tonometer that generates two indices which correspond to large artery elasticity (LAE) and small artery elasticity (SAE). LAE and SAE estimates by pulse waveform analysis have previously shown greater correlation to Framingham risk when directly compared with other techniques such as flow-mediated diltation, and both LAE and SAE are associated with traditional cardiovascular risk factors (smoking, insulin resistance, hypertension). It is unclear what the net effect of maraviroc, a chemokine-receptor blocker is on cardiovascular function. The aims of this substudy are: * To compare changes in the vascular endothelium between the control arm ((N(t)RTI) plus PI/r) and each of the maraviroc switch arms over 48 weeks of follow-up. * To compare the changes in biomarkers and selected immunological markers between the control arm ((N(t)RTI) plus PI/r) and each of the maraviroc switch arms over 48 weeks of follow-up.
Study Type
OBSERVATIONAL
Enrollment
34
tenofovir zidovudine abacavir lamivudine emtricitabine ritonavir darunavir atazanavir lopinavir fosamprenavir
maraviroc ritonavir darunavir atazanavir lopinavir fosamprenavir
maraviroc tenofovir zidovudine abacavir lamivudine emtricitabine
Hospital General de Agudos "Dr. José María Ramos Mejía"
Buenos Aires, Buenos Aires, Argentina
Fundacion IDEAA
Buenos Aires, Buenos Aires, Argentina
Hospital Italiano de Buenos Aires
Buenos Aires, Argentina
St. Vincent's Hospital
Sydney, New South Wales, Australia
Mean change in small arterial elasticity (SAE) as measure by pulse wave tonometry
measured at 6 timepoints week 0, 4, 12, 24, 48, 96
Time frame: 96 weeks
• Mean change in large arterial elasticity (LAE) as measure by pulse wave tonometry
measured at 6 timepoints, week 0,4,12,24,48,96
Time frame: 96 weeks
• Changes from baseline in selected soluble markers of immune activation, coagulation, vascular and platelet function
stored bloods from the main study will be used to explore changes in vascular biomarkers
Time frame: 96 weeks
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Johann Wolfgang Goethe-University Hospital, Medical HIVCENTER
Frankfurt, Frankfurt Am Main, Germany
Chulalongkorn University Hospital
Bangkok, Bangkok, Thailand