A Natural History Study of Novel Biomarkers in Pulmonary Arterial Hypertension
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Enrollment
- 270
- Locations
- 1
- Primary Endpoint
- Examine whether any novel test (inflammatory markers or high resolution cardiac MRI), accurately classifies PAH subjects according to disease severity as assessed by their baseline 6-minute walk distance.
Study Overview
Brief Summary
Background:
- High blood pressure in the lungs, known as pulmonary arterial hypertension (PAH), is a rare disorder. Some people have disease-associated PAH and some have PAH from an unknown cause. Researchers want to follow the natural history of all PAH patients to understand how PAH progresses in order to discover targets for future research into new treatments. To further identify treatment targets, they will compare healthy volunteers to patients with PAH.
Objectives:
- To study the natural history of PAH.
Eligibility:
- Individuals at least 18 years of age who have PAH.
- Healthy volunteers at least 18 years of age.
Design:
- Participants with PAH will have periodic visits to the National Institutes of Health Clinical Center. After the first visit, they will return in 6 months and then yearly or every other year for as long as the study continues.
- The first visit will take up to 3 days. It will involve the following tests:
- Physical exam and medical history
- Blood and urine samples
- Heart and lung function tests and imaging studies
- Six-minute walk test
- Questions about exercise and physical activity
- Healthy volunteers will have only one visit to the Clinical Center, during which they will undergo screening tests, and complete many of the same tests as patients with PAH
Detailed Description
Introduction:
Pulmonary arterial hypertension (PAH) is a rare disorder associated with poor survival. Endothelial dysfunction resulting from 1) genetic susceptibility, and 2) a triggering stimulus that initiates pulmonary vascular injury, the "two-hit" hypothesis, appears to play a central role both in the pathogenesis and progression of PAH. Inflammation appears to drive this dysfunctional endothelial phenotype, propagating cycles of injury and repair in genetically susceptible patients with idiopathic PAH (IPAH) and patients with disease-associated PAH. However, despite mounting evidence of vascular inflammation in patients with PAH, detailed phenotypic studies are lacking on the temporal evolution of this process and its contribution to right ventricular (RV) and pulmonary vascular remodeling. We hypothesize that a detailed characterization of the temporal evolution of vascular inflammation in PAH and its impact on RV and pulmonary vascular function will add prognostic value to traditional measures of disease severity and suggest novel therapeutic targets for future research.
Objectives:
Patients with IPAH and disease-associated PAH will be recruited to the NIH and enrolled in this natural history study investigating the ability of circulating markers of vascular inflammation as well as high-resolution cardiac magnetic resonance imaging (MRI) to accurately stage severity of disease and/or predict clinically relevant outcomes.
Methods:
Study Design
- Study Type
- Observational
- Observational Model
- Case Control
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 100 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •ELIGIBILITY:
- •The study will enroll subjects with confirmed and suspected NYHA/WHO Group 1 PH (68) as well as age and sex matched control subjects. Subjects must be at least 18 years of age and must be able to provide informed, written consent for participation in this study. There is no exclusion based on race or sex.
- •INCLUSION AND
Exclusion Criteria
- •FOR PAH SUBJECTS:
- •Inclusion Criteria:
- •The following parameters on RHC are required to meet the hemodynamic definition of PAH (NYHA/WHO Group I PH):
- •mean pulmonary artery pressure of > 25 mmHg at rest,
- •pulmonary capillary wedge pressure of < 15 mmHg (or a left ventricular end-diastolic pressure of < 12 mmHg), and
- •pulmonary vascular resistance of > 3 Wood units (240 dyn s cm-5).
- •For patients with suspected PAH (Group I PH) who have not undergone a RHC and/or additional testing to confirm the diagnosis, this testing will be completed as clinically indicated under a procedural consent. If clinically indicated (diagnostic) testing indicates that the subject with suspected PAH does not in fact meet standard criteria for PAH (Group I PH), then the subject will be removed from the study.
- •Exclusion Criteria:
- •Pregnant or breastfeeding women (all women of childbearing potential will be required to have a screening urine or blood pregnancy test)
- •Age less than 18 years
- •Inability to provide informed written consent for participation in the study
- •INCLUSION AND EXCLUSION CRITERIA FOR HEALTHY CONTROL SUBJECTS:
- •Inclusion Criteria for Control Subjects
- •Any healthy man or woman who is the appropriate age and sex for matching to a PAH patient
- •Must be eligible for MRI and Gadolinium Based MRI studies
- •Must be eligible for CT and Iodine Based Contrast CT studies
- •Exclusion Criteria for Healthy Control Subjects
- •Current pregnancy or breastfeeding (All women of childbearing potential will be required to have a screening urine or blood pregnancy test)
- •Electrocardiographic evidence of clinically relevant heart disease
- •Symptoms of coronary or cardiac insufficiency
- •More than one major risk factor for coronary artery disease (excluding age and sex)
- •Obesity (defined as a body mass index > 30 kg/m^2)
- •History of underlying conditions/risk factors associated with pulmonary hypertension such as collagen vascular disease, HIV infection, use of appetite suppressants, chronic liver disease or cirrhosis of the liver, chronic thromboembolic disease, congenital heart defects, hypoxemia and/or significant pulmonary parenchymal disease
- •Systemic hypertension that is not well controlled (i.e. blood pressure at the time of screening >140/90 mmHg in adults < 60 years old or >150/90 mmHg in adults 60 years or older) on medications. Subjects taking > 2 anti-hypertensive medications will be excluded irrespective of their current blood pressure at time of screening
- •Anemia, thrombocytopenia or coagulopathy
- •Renal insufficiency (defined as an estimated glomerular filtration rate of < 60 mL/min/1.73m^2 of body surface area)
- •Active tobacco use (> 6 months) in the past ten years, any tobacco use within 3 months prior to the screening evaluation or any tobacco use prior to completion of the study
- •Inability to provide informed written consent for participation in the study
- •History of recreational drug use with the exception of marijuana (as long as marijuana use was > 3 months from the time of study screening).
- •Volunteers may be excluded if in the opinion of the study investigators they have a condition that may adversely affect the outcome of the study or the safety of the volunteer.
- •Exclusion Criteria for MRI in Healthy Control Subjects and Subjects with PAH
- •These contraindications include but are not limited to the following devices or conditions:
- •Implanted cardiac pacemaker or defibrillator
- •Cochlear Implants
- •Ocular foreign body (e.g. metal shavings)
- •Embedded shrapnel fragments
- •Central nervous system aneurysm clips
- •Implanted neural stimulator
- •Any implanted device that is incompatible with MRI
- •Unsatisfactory performance status as judged by the referring physician such that the subject could not tolerate an MRI scan. Examples of medical conditions that would not be accepted would include unstable angina and severe dyspnea at rest
- •Subjects requiring monitored sedation for MRI studies
- •Subjects with a condition precluding entry into the scanner (e.g. morbid obesity, claustrophobia, etc.)
- •Subjects with severe back-pain or motion disorders who will be unable to tolerate supine positioning within the MRI scanner and hold still for the duration of the examination.
- •Exclusion Criteria for Gadolinium Based MRI Studies Only:
- •History of severe allergic reaction to gadolinium contrast agents despite pre- medication with diphenhydramine and prednisone
- •Chronic kidney disease (an estimated glomerular filtration rate of < 60 mL/min/1.73m^2 of body surface area)
- •Exclusion Criteria for Cardiac Computed Tomography in Healthy Control Subjects and Subjects with PAH:
- •1) Subjects with a condition precluding entry into the scanner (e.g. morbid
- •obesity, claustrophobia, etc.)
- •Exclusion Criteria for Iodine Based Contrast CTA Studies Only:
- +4 more not shown
Arms & Interventions
Healthy Volunteers
Enroll up to 120 healthy volunteers, in order to obtain approximately 55 evaluable healthy volunteers matched to pulmonary arterial hypertension subjects for age and sex
Pulmonary Arterial Hypertension Subjects
150 subjects with pulmonary arterial hypertension; male or female, age grater than or equal to 18 - 99 years
Outcomes
Primary Outcomes
Examine whether any novel test (inflammatory markers or high resolution cardiac MRI), accurately classifies PAH subjects according to disease severity as assessed by their baseline 6-minute walk distance.
Time Frame: 10 years
Compare outcomes in PAH subjects with controls
Secondary Outcomes
No secondary outcomes reported