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- Title
Shared and Distinct Genomics of Chronic Thromboembolic Pulmonary Hypertension and Pulmonary Embolism.
- Authors
Liley, James; Newnham, Michael; Bleda, Marta; Bunclark, Katherine; Auger, William; Barbera, Joan Albert; Bogaard, Harm; Delcroix, Marion; Fernandes, Timothy M.; Howard, Luke; Jenkins, David; Lang, Irene; Mayer, Eckhard; Rhodes, Chris; Simpson, Michael; Southgate, Laura; Trembath, Richard; Wharton, John; Wilkins, Martin R.; Gräf, Stefan
- Abstract
Rationale: Chronic thromboembolic pulmonary hypertension involves the formation and nonresolution of thrombus, dysregulated inflammation, angiogenesis, and the development of a small-vessel vasculopathy. Objectives: We aimed to establish the genetic basis of chronic thromboembolic pulmonary hypertension to gain insight into its pathophysiological contributors. Methods: We conducted a genome-wide association study on 1,907 European cases and 10,363 European control subjects. We coanalyzed our results with existing results from genome-wide association studies on deep vein thrombosis, pulmonary embolism, and idiopathic pulmonary arterial hypertension. Measurements and Main Results: Our primary association study revealed genetic associations at the ABO, FGG, F11, MYH7B, and HLA-DRA loci. Through our coanalysis, we demonstrate further associations with chronic thromboembolic pulmonary hypertension at the F2, TSPAN15, SLC44A2, and F5 loci but find no statistically significant associations shared with idiopathic pulmonary arterial hypertension. Conclusions: Chronic thromboembolic pulmonary hypertension is a partially heritable polygenic disease, with related though distinct genetic associations with pulmonary embolism and deep vein thrombosis.
- Subjects
PULMONARY embolism; PULMONARY arterial hypertension; VENOUS thrombosis; THROMBOEMBOLISM; PULMONARY hypertension; GENOME-wide association studies; ABO blood group system
- Publication
American Journal of Respiratory & Critical Care Medicine, 2024, Vol 209, Issue 12, p1477
- ISSN
1073-449X
- Publication type
Article
- DOI
10.1164/rccm.202307-1236OC