Dysregulation of Lipid Metabolism and Right Ventricular Function in PAH



Status:Enrolling by invitation
Conditions:High Blood Pressure (Hypertension)
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:8/18/2018
Start Date:January 2015
End Date:June 2019

Use our guide to learn which trials are right for you!

Right ventricular (RV) failure is the predominant cause of death in pulmonary arterial
hypertension (PAH). No RV-specific therapies are available, in part because the underlying
mechanisms of RV dysfunction are poorly understood. Given the heart's preference for fatty
acids (FA) as an energy source, a deeper understanding of FA metabolism may shed light on RV
adaptation to elevated afterload in PAH. The purpose of this study is to test the hypothesis
that defects in fatty acid metabolism are common in PAH and contribute to RV failure. The
investigators will measure peripheral and transcardiac lipid and glucose metabolites in PAH
patients in comparison with patients with pulmonary venous hypertension and no evidence of
pulmonary hypertension. The investigators will also correlate metabolites with concurrent
measurement of right ventricular function.


Inclusion Criteria:

- ≥ 18 years old

- Scheduled to undergo cardiac catheterization (right ± left heart catheterization)
and/or electrophysiology study in the VHVI cardiac catheterization laboratory
(CCL)/electrophysiology laboratory (EP lab)

- Hemoglobin value ≥ 10 g/dL or hematocrit of ≥ 30% (measured on clinically-indicated
blood draw within 30 days or a point-of-care measurement in CCL/EP Laboratory if
clinically-indicated value is not available)

Exclusion Criteria:

- Any individual that is anemic and has a hemoglobin value < 10 g/dL and hematocrit of <
30% will be excluded from the study.

- If a physician performing the procedure believes that performing the extra steps and
/or acquiring the additional blood samples will delay or otherwise compromise
participants' care, he/she can abandon acquisition of those data at his/her
discretion.

- Contraindication to cardiac MRI (applies only to patients undergoing CMR as part of
this protocol).

- Implanted ferromagnetic material

- Glomerular filtration rate < 60mL/min (measured on clinically-indicated blood
draw within 30 days of CMR or a point-of-care measurement in the CMR Laboratory
if clinically-indicated GFR is not available)
We found this trial at
1
site
Nashville, Tennessee 37232
?
mi
from
Nashville, TN
Click here to add this to my saved trials