MedPath

Pulmonary Vascular Disease Phenomics Program PVDOMICS

Active, not recruiting
Conditions
Pulmonary Arterial Hypertension
Interventions
Other: No Intervention
Registration Number
NCT02980887
Lead Sponsor
The Cleveland Clinic
Brief Summary

It is recognized that patients with various forms of heart and lung disease exhibit varying degrees of pulmonary hypertension, pulmonary vascular remodeling, and right ventricular dysfunction. The genetic, molecular, and cellular processes driving these phenomena are not well understood. Rapid advances in high throughput omic methodology, combined with powerful bioinformatics and network biology capability, have created the opportunity to conduct studies that broadly search for homologies and differences across the spectrum of disease states associated with pulmonary hypertension, and determinants of the spectrum of right ventricular compensation that accompanies these conditions

Detailed Description

The protocol is designed to lead to new understanding of patients with pulmonary hypertension and right heart dysfunction, based on molecular, clinical, hemodynamic and radiographic characteristics. New classifications will be a product of association of these in depth phenotypic descriptions with specific molecular mechanisms of pathogenesis. The protocol will be implemented to lead to identification of both sub-phenotypes of lung vascular disease and to biomarkers of disease that may be useful for early diagnosis or for assessment of interventions to prevent or treat this condition.

A longitudinal study in a subset of the participants enrolled in the parent cross-sectional study will:

1. Retest participants at a minimum 6 month interval from initial evaluation to collect a core set of clinical and OMICS features. This will include survival, clinical staging, clinical group assignment, 6-minute walk, echocardiography, and blood for a broad collection of selected OMICS tests, to include proteomics and other variables found to be informative in the initial set.

2. Associate and compare OMICS data with clinical sets and OMICS clusters between baseline and follow-up interval, with attention to reproducibility, predictive capacity as biomarkers for diagnosis, disease progression, phenotypic changes, functional capacity, therapeutic response and survival.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
1195
Inclusion Criteria

Patients ages >18 years of age referred for right heart catheterization for further evaluation of known PVD or to be at risk for PVD due to established cardiac disease or pulmonary disease

  • Able to perform complete diagnostic testing listed subsequently (cardiac catheterization, echo, exercise test, PFT's, ECG, chest CT, quality of life questionnaires, ventilation/perfusion scan, cardiac MRI, body composition bioimpedance, and sleep study)
  • Subject signs informed consent to perform required testing for the protocol
Exclusion Criteria

Dialysis dependent renal function; In the clinician's opinion, too ill to perform the protocol testing; Pregnant or nursing

Longitudinal study:

Inclusion Criteria:

  • Any PH, comparators or control participant previously enrolled in the parent PVDOMICS protocol with a minimum of six months post-enrollment
  • Dialysis dependent renal function since the parent study acceptable

Exclusion Criteria:

Participant Level 1 (clinic visit):

  • Transplant other than heart or lung
  • In the clinician's opinion, too ill to perform L-PVDOMICS testing even if limited testing.
  • Participants who withdrew from the parent PVDOMICS study
  • Pregnant or nursing
  • Concurrent participation in any investigational drug study or other clinical trial

Participant Level 2 (telephone visit):

  • Transplant other than heart or lung
  • Participants who withdrew from the parent PVDOMICS study

Participant Level 3 (medical chart review):

  • Participants who withdrew from the parent PVDOMICS study

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Pulmonary Vascular DiseaseNo InterventionPulmonary Vascular Disease at risk for pulmonary hypertension
Pulmonary HypertensionNo InterventionThose meeting WSPH/WHO group classifications 1-5 of pulmonary hypertension
ControlsNo InterventionHealthy controls No intervention as this is an observational study
Primary Outcome Measures
NameTimeMethod
Precision based definitions of pulmonary vascular diseases (PVD)Over 5 years

OMICs analyses will be used to assign new class of PVD

Secondary Outcome Measures
NameTimeMethod
Identification of biomarkers for PVD5 years

OMICs and other measures of disease

Trial Locations

Locations (7)

New York Medical College

🇺🇸

Valhalla, New York, United States

University of Arizona Health Sciences Center

🇺🇸

Tucson, Arizona, United States

Johns Hopkins University School of Medicine

🇺🇸

Baltimore, Maryland, United States

Brigham and Women's Hospital

🇺🇸

Boston, Massachusetts, United States

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

Weill Cornell Medicine

🇺🇸

New York, New York, United States

Vanderbilt University Medical Center

🇺🇸

Nashville, Tennessee, United States

© Copyright 2025. All Rights Reserved by MedPath