Chronic Thromboembolic Pulmonary Hypertension
Conditions
Brief summary
Some patients who have blood clots come down with a life-threatening condition known as Chronic Thromboembolic Pulmonary Hypertension (CTEPH), which is high blood pressure only in the arteries of the lungs. This study seeks to understand more about the genetics causes of CTEPH by obtaining blood samples and examining family histories.
Detailed description
This project proposes to identify a cohort of Utah patients with CTEPH, and to perform a comprehensive analysis of family history and CTEPH risk factors in these patients, and in controls with acute pulmonary embolism (PE) and pulmonary arterial hypertension (PAH). Detailed family history interviews will be performed with all patients, and all enrolled patients will provide a blood sample for thrombophilia testing and for gene sequencing with the goal of identifying novel genetic variants that contribute to CTEPH risk.
Interventions
OTHERBlood Draw
Sponsors
Intermountain Health Care, Inc.
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* CTEPH cohort: 1. Confirmed CTEPH based on having undergone PEA surgery. 2. Strongly suspected CTEPH based on right heart catheterization data showing mPAP\>26 and PCWP\<15, and imaging demonstrating chronic thromboembolic disease (either ventilation/perfusion scan, CT pulmonary angiography, or conventional pulmonary angiography). * PE cohort: 1. PE diagnosed by CT pulmonary angiography or ventilation/perfusion scan within the preceding 24 months. 2. No evidence of PH at the time of enrollment (based on absence of dyspnea, exertional chest pain, or exertional presyncope on history, lack of physical exam findings of PH or right heart failure, and lack of signs of PH on objective data including echocardiography and/or right heart catheterization). 3. No evidence of chronic thromboembolic disease at the time of enrollment (based on chronic appearing thrombus on CT pulmonary angiography or conventional pulmonary angiography, or based on prior high probability ventilation/perfusion scan showing a similar pattern of perfusion defects). * PAH cohort: 1. Diagnosis of group 1 PAH. 2. Prior normal or low probability ventilation/perfusion scan. 3. No reported history of prior VTE events. 4. If available, all prior evaluations for VTE (including CT pulmonary angiography and Doppler ultrasound exams) must also be negative.
Exclusion criteria
* Under the age of 18
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rates of family history of VTE in relatives of CTEPH patients compared to PE and PAH patients in Intermountain populations | through study completion, approximately 18 months |
Secondary
| Measure | Time frame |
|---|---|
| Characteristics of familial and, apparently, sporadic CTEPH in Intermountain populations | through study completion, approximately 18 months |
| Estimates of prevalence of familial CTEPH in Intermountain populations | through study completion, approximately 18 months |
| Heritability and penetrance patterns of familial CTEPH | through study completion, approximately 18 months |
| Discovery and validation of genetic polymorphisms present in familial CTEPH patients | through study completion, approximately 18 months |
| Identification of gene pathways that may be relevant to the development of CTEPH after actue PE | through study completion, approximately 18 months |
Countries
United States
Contacts
Primary ContactValerie T Aston, MBA
Backup ContactDavid P Tomer, MS
Outcome results
None listed