HIV Clinical Trial
Official title:
Evaluation of Endothelial and Hemodynamic Function in HIV Associated Pulmonary Hypertension and a Phase I/II Safety and Efficacy Trial of Sildenafil in HIV Associated Pulmonary Hypertension
This study will examine how blood pressure in the lungs is controlled in healthy people,
people with HIV and people with HIV and pulmonary artery hypertension (high blood pressure in
the lungs, also called PAH). PAH sometimes develops in people with HIV, but it is not known
why this occurs or how best to treat it.
Healthy volunteers and patients with HIV infection who are 18 years of age or older may be
eligible for this study. All candidates are screened with a medical history, physical
examination, electrocardiogram (EKG), chest x-ray, echocardiogram and blood tests.
Participants undergo the following procedures:
All participants have a right heart catheterization and forearm blood flow study.
- Catheterization study. A catheter (plastic tube) is placed in an arm vein and possibly
in an artery in the arm. Then a large catheter is passed through a vein in the groin,
neck or chest. Through this "introducer" catheter, another catheter is advanced into the
right side of the heart and to the pulmonary artery. A facemask is put in place to
measure the amount of nitric oxide produced by the lungs. Acetylcholine is infused
through the catheter and its effects on blood pressure in the lungs and on the amount of
nitric oxide exhaled is measured. After about 1 hour, the catheter and facemask are
removed and a new catheter is inserted through the introducer catheter into the
pulmonary artery. The subject is moved into an MRI scanner where blood flow is measured
after infusion of three different medications: acetylcholine (causes blood vessels to
expand and slows heart rate); sodium nitroprusside (causes blood vessels to expand and
increases blood flow to the heart); and L-NMMA (decreases blood flow by blocking
production of nitric oxide in cells lining the blood vessels).
- Blood flow study. Small tubes are inserted into the artery of the patient's forearm.
These are used to infuse medicines and draw blood samples. Forearm blood flow is
measured using pressure cuffs placed on the wrist and upper arm, and a strain gauge (a
rubber band device) placed around the forearm. When the cuffs are inflated, blood flows
into the arm, stretching the strain gauge, and the flow measurement is recorded. A small
lamp is positioned over the hand to measure the light reflected from the hand and blood
flow in the forearm. Blood samples are then drawn to measure blood counts and proteins
and other natural body chemicals. Then, forearm blood flow is measured after
administration of small doses of sodium nitroprusside, acetylcholine and L-NMMA. There
is a 20- to 30-minute rest period between injections of the different drugs.
In addition, HIV-infected patients with PAH undergo the following tests to determine the
cause of their PAH: CT scan of the lungs, pulmonary function tests, 6-minute walk test,
quality-of-life assessment, assessment of difficulty in breathing, exercise testing while
measuring oxygen breathed in and carbon dioxide breathed out, blood tests, monitoring of
oxygen saturation during sleep for 1 night and ventilation/perfusion scan. For the
ventilation/perfusion scan, the subject breathes in a small amount of radioactive aerosol
while images are obtained of the radioactivity as it enters the lungs, and then pictures of
the lungs are taken from multiple angles. Next, the patient receives an injection of tiny
particles of albumin (a protein) containing a small amount of radioactivity and pictures of
the lungs are taken that show the pattern of blood flow to the lungs.
Patients with HIV and PAH who may benefit from the investigational drug, sildenafil (commonly
known as Viagra), may continue to participate in the next stage of the study. They receive
the first dose of sildenafil after completing the forearm blood flow study. They continue the
drug for 16 weeks, returning to the clinic 1 week after the first dose and then every other
week to monitor the response to treatment and drug side effects. At the end of 16 weeks,
patients return to the clinic for a repeat evaluation, including blood tests, 6-minute walk
test, echocardiogram, right heart catheterization and forearm blood flow study.
...
HIV infection has been associated with an increased prevalence of pulmonary hypertension. In
addition, recent data suggests that a state of endothelial dysfunction develops in HIV
disease secondary to anti-retroviral therapy and associated dyslipidemia or secondary to
direct viral infection of the endothelium. This leads to premature atherosclerosis and
possibly contributes to avascular necrosis of the hip. Similar effects on the pulmonary
vasculature may be involved in the development of pulmonary vasculopathy.
In this study we plan to invasively characterize the status of pulmonary and systemic
endothelial function and determine the mechanisms of pulmonary vascular endothelial
dysfunction in HIV disease. To this end we will catheterize healthy volunteers and volunteers
with HIV infection with and without pulmonary hypertension and directly measure
acetylcholine-dependent blood flow in the pulmonary and brachial artery to assess pulmonary
and systemic endothelium-dependent blood flow. Simultaneous measurement of exhaled NO and
pulmonary capillary artery NO2 - will allow for complete characterization of the contribution
of NO production to endothelium-dependent vasomotor control. We will also use recently
developed MRI techniques to measure pulmonary artery blood flow during infusion of
acetylcholine (ACH), sodium nitroprusside (SNP) and NG monomethyl-L-arginine (LNMMA) to
establish responsiveness to an endothelium dependent vasodilator, endothelium-independent
vasodilator and an NO inhibitor, respectively. Volunteers with pulmonary hypertension will
have the option to undergo open label phase I/II treatment with sildenafil for 16 weeks and
return for a repeat assessment of pulmonary hemodynamics as well as pulmonary and systemic
endothelial function.
Endothelial cells will be isolated using novel flow-cytometry methodologies developed over
the last two years at the NIH intramural division utilizing combinations of positive and
negative selection based on specific surface markers for activated T cells and endothelial
cells and markers of cell viability. Endothelial cells will subsequently be interrogated
using amplified real time PCR methodologies and affymetrix based gene expression profiling
developed in our laboratories. The levels of expression in endothelial cells of HIV virus,
HHV8, eNOS, caveolin, HO-1, endothelin receptors A and B, and endothelin 1, in addition to
other proteins regulating vascular homeostasis and cellular host defense (i.e. epidermal
growth factor, transforming growth factor beta, platelet derived growth factor and
interleukin-6), will be assessed.
These studies will provide insights into the mechanisms of pulmonary artery endothelial
dysfunction and suggest rationally designed therapies targeting viral load, HHV8, and/or the
NO/endothelin pathways. These studies have the promise of opening the door to the study of
pulmonary artery endothelial dysfunction at the physiological, cellular and molecular level.
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