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Right Ventricular Metabolism in Pulmonary Arterial Hypertension

Metabolic Intervention in the Right Ventricle in Pulmonary Arterial Hypertension

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02763735
Enrollment
34
Registered
2016-05-05
Start date
2014-06-30
Completion date
2019-06-30
Last updated
2020-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy, Pulmonary Arterial Hypertension

Keywords

Pulmonary arterial hypertension, Right ventricle, Right ventricular function, Metabolism, Non-invasive imaging, Healthy Subjects

Brief summary

The purpose of this study is to use non-invasive imaging to determine the metabolic phenotype of the right ventricle in patients with pulmonary arterial hypertension across a spectrum of disease severity.

Detailed description

Current medical therapy for pulmonary arterial hypertension (PAH) is aimed at reducing pulmonary vascular resistance (PVR) but not ameliorating right ventricular (RV) failure, the major cause of death. There are no RV-specific therapies currently available for PAH, in part because the pathophysiology of RV failure is poorly understood. The investigators hypothesize that the RV in PAH develops a distinct metabolic pattern characterized by increased glycolysis, impaired oxidative metabolism and lipid deposition, which are associated with RV failure. Specific Aim 1. To test the hypothesis that the RV in human PAH exhibits lipid deposition, increased glycolysis and impaired fatty acid oxidation. The investigators will measure RV oxidative metabolism and glycolysis in PAH patients and controls using positron emission tomography 11C acetate and \[18F\]fluoro-deoxy-D-glucose imaging and measure myocardial lipid accumulation using magnetic resonance spectroscopy imaging. Specific Aim 2. To test the hypothesis that an abnormal RV metabolic profile is associated with RV dysfunction and reduced exercise capacity in PAH. PET and MRS findings will be correlated with RV function, patient exercise capacity and a blood metabolic profile.

Interventions

None listed

Sponsors

Vanderbilt University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Heritable or idiopathic PAH * 18 years or older * Able to give informed consent

Exclusion criteria

* Pregnancy * Type 1 diabetes mellitus * Prednisone use * PAH associated with any condition other than idiopathic or heritable * Implanted ferromagnetic material incompatible with MRI

Design outcomes

Primary

MeasureTime frameDescription
Right ventricular oxygen consumption divided by the rate pressure productAt time of C11 acetate PET scankmono divided by the rate pressure product (heart rate X systolic blood pressure)

Secondary

MeasureTime frameDescription
Right ventricular glucose uptake (standardized uptake value)At time of 18-FDG PET scan
Percent myocardial triglyceride contentAt time of cardiac magnetic resonance imagingPercent of myocardial triglyceride measured in the interventricular septum
Right ventricular oxygen consumption (kmono)At time of C11 acetate PET scan
Correlation of kmono, kmono/RPP, FDG uptake, and myocardial triglyceride content with six minute walk distanceDay 1
Correlation of kmono, kmono/RPP, FDG uptake, and myocardial triglyceride content with plasma metabolic profileDay 1
Correlation of kmono, kmono/RPP, FDG uptake, and myocardial triglyceride content with right ventricular functionDay 1

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026