Trial record 7 of 407 for:    PAH

Hormonal, Metabolic, and Signaling Interactions in PAH

This study is currently recruiting participants.
Verified April 2014 by Vanderbilt University
Sponsor:
Information provided by (Responsible Party):
Jim Loyd, Vanderbilt University
ClinicalTrials.gov Identifier:
NCT01884051
First received: January 15, 2013
Last updated: April 3, 2014
Last verified: April 2014
  Purpose

Our hypothesis is that optimal treatment of the dysfunctional metabolic pathways which underlie PAH will improve pulmonary vascular function and consequences of the disease.


Condition
Idiopathic Pulmonary Arterial Hypertension
Heritable Pulmonary Arterial Hypertension
Scleroderma Associated Pulmonary Arterial Hypertension
Appetite Suppressant Associate PAH

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Hormonal, Metabolic, and Signaling Interaction in Pulmonary Arterial Hypertension

Resource links provided by NLM:


Further study details as provided by Vanderbilt University:

Primary Outcome Measures:
  • Ratio of sex hormone metabolites [ Time Frame: 5 years ] [ Designated as safety issue: No ]
    The primary outcome measure is the ratio of 2-hydroxyestrogens to 16-hydroxyestrogens among patients compared to both controls and at risk but well subjects.

  • Evaluation of insulin resistance in pulmonary arterial hypertension patients/Clinical trial of Metformin in Pulmonary Arterial Hypertension [ Time Frame: 5 years ] [ Designated as safety issue: No ]
    We will assess various measures of insulin resistance among patients, compared to healthy control subjects as well as at risk but well subjects. The primary measure will be assessed using the glucose clamp technique to quantify insulin secretion and resistance.

  • Mechanism, safety, and efficacy of ACE-2 in the treatment of PAH. [ Time Frame: 5 years ] [ Designated as safety issue: Yes ]
    We will assess the safety and efficacy of ACE-2 for the treatment of established PAH. Primary outcome measure will be the six-minute walk test to determine subject improvement or clinical worsening.

  • Clinical Trial of Metformin in Pulmonary Arterial Hypertension [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]

    Specific Aim 1. To test the hypothesis that metformin will ameliorate oxidant stress in pulmonary arterial hypertension Primary safety endpoint: absence of lactic acidosis, withdrawal from the study if attributed to metformin Primary efficacy endpoint: change in urinary and plasma oxidant stress measures (F2 isoprostanes and metabolites, isofurans, and nitrotyrosine)

    Specific Aim 2. To test the hypothesis that metformin will decrease myocardial lipid content, increase oxidative metabolism and decrease glucose uptake.

    Primary Endpoints: change in myocardial percent triglycerides (%TGs), kmono/RPP of C11 acetate, and uptake of FDG before and after metformin.



Secondary Outcome Measures:
  • Mechanism, safety, and efficacy of ACE-2 in the treatment of PAH. [ Time Frame: 5-year ] [ Designated as safety issue: Yes ]
    Secondary outcomes will be hemodynamics measured by right heart catheterization and PET Scans to measure organ specific changes in metabolites known to be disrupted by PAH.

  • Clinical Trial of Metformin in Pulmonary Arterial Hypertension [ Time Frame: 3 years ] [ Designated as safety issue: No ]

    Specific Aim 1. To test the hypothesis that metformin will ameliorate oxidant stress in pulmonary arterial hypertension

    Secondary Endpoints: lung cellular proliferation as measured by FDG avidity, change in the markers of insulin resistance and sensitivity, BMPR2 expression in peripheral blood mononuclear cells, and change in glucose and lipid metabolites.

    Specific Aim 2. To test the hypothesis that metformin will decrease myocardial lipid content, increase oxidative metabolism and decrease glucose uptake.

    Secondary Endpoints: change in RVEF, RV mass index, insulin resistance and sensitivity indices, glucose and lipid metabolites, and six-minute walk distance (6MWD)



Biospecimen Retention:   Samples With DNA

We plan to collect the following samples on all subjects:

DNA, RNA, white cells, plasma, serum, urine

We plan to collect the following samples on selected subjects:

Skin biopsy


Estimated Enrollment: 2120
Study Start Date: September 2012
Estimated Study Completion Date: September 2017
Estimated Primary Completion Date: December 2016 (Final data collection date for primary outcome measure)
Groups/Cohorts
PAH patients
Patients diagnosed with WHO Group 1 PAH
Healthy subjects
Subjects who have been evaluated for heart and lung disease and found to be healthy

Detailed Description:

Project 1: This project will work to understand why women are affected by pulmonary arterial hypertension (PAH) so much more often than men. This observation is true in heritable, idiopathic and associated forms of PAH. While males and females have some similar hormone levels, certain hormones exist at higher levels in each gender. For example, estrogen levels are much higher in females, and thus seemed the most sensible place to start looking for differences that may be affecting disease. In a small, early study of our heritable patients, we found differences in how patients break down estrogens as compared to healthy control subjects. Now, we want to confirm that what we found is true in a much larger group of patients that includes idiopathic and associated forms of PAH. We will also look to see if testosterone and other androgenic hormones are somehow protective for males. If the observation holds true in the larger group of patients, then we may try to "fix" the hormone imbalance in a mouse model of PAH with a drug therapy, and see if it helps improve the mouse pulmonary hypertension without bad side effects to the animals. If the animal drug studies work, then we may be able to try this drug in patients to see if it will work as a human treatment.

Project 2: Despite major advances in understanding PAH in recent decades, safe, effective and tolerable therapies remain elusive. The metabolic syndrome (central obesity, insulin resistance, high blood pressure and hyperlipidemia—fats in the blood) has been implicated in PAH. Treating the downstream consequences of insulin resistance in the pulmonary vasculature is a new approach to effective intervention against this highly mortal disease. This project will study the role of insulin resistance in pulmonary arterial hypertension and determine if therapies to treat insulin resistance will improve pulmonary arterial hypertension.

Project 3: In Project 3, we are working on the theory that PAH can be treated by fixing cell-cell junctions in blood vessels with a drug called recombinant ACE2(angiotensin converting enzyme 2). This is the only approach so far that has worked to reverse disease in mouse models of heritable PAH, but we need to better understand how it is working and make sure it has long term safety in animal models before starting human trials, hopefully within a few years. Definition: Cell-cell junctions-all of our organs and body structures are made from cells. Normally, these cells (think of a balloon filled with water) line up right next to each other so that the cell membranes touch each other. Materials can flow from one cell to the next. In PAH patients it is believed that the cells in the linings of the small arteries are not able to line up together as they should.

  Eligibility

Ages Eligible for Study:   up to 90 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Cohort 1 subjects will be recruited from our adult and pediatric pulmonary vascular disease clinics. Cohort 2-healthy controls will be recruited form patients families and the general public in middle Tennesssee.

Criteria

Inclusion Criteria:

Project 1

Inclusion:

  1. Diagnosis of IPAH (idiopathic pulmonary arterial hypertension), HPAH (heritable pulmonary arterial hypertension), or APAH (associated pulmonary arterial hypertension), family members of affected persons
  2. Age 0-90, age 12-90 for skin biopsy

Exclusion:

  1. Other diagnosis
  2. Age greater than 90, age less than 12 or greater than 90 for skin biopsy

Project 2

Inclusion:

  1. Diagnosis of IPAH, HPAH, or APAH, family members of affected persons
  2. 0-90
  3. Subjects with reasonably easy access to clinic for blood collection and other testing
  4. Subject able to tolerate fasting state prior to sample collection and EndoPAT (endothelial function assessment) testing

Exclusion:

  1. Other diagnosis
  2. 0-90
  3. Subjects with difficulty reaching clinic for blood collection and other testing
  4. Subjects unable to tolerate fasting state

Project 3

Inclusion:

  1. Diagnosis of IPAH, HPAH, or APAH, family members of affected persons
  2. 7-90

Exclusion:

  1. Other diagnosis
  2. Age less than 7 or greater than 90

    -

    Exclusion Criteria:

    -

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01884051

Contacts
Contact: Lisa Wheeler, BSMT 800-288-0378 lisa.wheeler@vanderbilt.edu
Contact: Errine Garnett, BA 615-343-0539 errine.t.garnett@vanderbilt.edu

Locations
United States, Tennessee
Vanderbilt University Medical Center Recruiting
Nashville, Tennessee, United States, 37232
Sponsors and Collaborators
Vanderbilt University
Investigators
Principal Investigator: James E Loyd, MD Vanderbilt University
  More Information

Publications:
Responsible Party: Jim Loyd, Professor of Medicine, Vanderbilt University
ClinicalTrials.gov Identifier: NCT01884051     History of Changes
Other Study ID Numbers: PO1 HL108800
Study First Received: January 15, 2013
Last Updated: April 3, 2014
Health Authority: United States: Vanderbilt Human Research Protection Program
United States: NIH-National Heart, Lung, Blood Institute

Keywords provided by Vanderbilt University:
Pulmonary arterial hypertension

Additional relevant MeSH terms:
Hypertension, Pulmonary
Scleroderma, Systemic
Scleroderma, Diffuse
Hypertension
Lung Diseases
Respiratory Tract Diseases
Connective Tissue Diseases
Skin Diseases
Vascular Diseases
Cardiovascular Diseases

ClinicalTrials.gov processed this record on April 15, 2014