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.
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.
Study Type
OBSERVATIONAL
Enrollment
260
Intermountain Medical Center
Murray, Utah, United States
RECRUITINGRates of family history of VTE in relatives of CTEPH patients compared to PE and PAH patients in Intermountain populations
Time frame: through study completion, approximately 18 months
Characteristics of familial and, apparently, sporadic CTEPH in Intermountain populations
Time frame: through study completion, approximately 18 months
Estimates of prevalence of familial CTEPH in Intermountain populations
Time frame: through study completion, approximately 18 months
Heritability and penetrance patterns of familial CTEPH
Time frame: through study completion, approximately 18 months
Discovery and validation of genetic polymorphisms present in familial CTEPH patients
Time frame: through study completion, approximately 18 months
Identification of gene pathways that may be relevant to the development of CTEPH after actue PE
Time frame: through study completion, approximately 18 months
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