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Shared and Distinct Genomics of Chronic Thromboembolic Pulmonary Hypertension and Pulmonary Embolism.

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; Morrell, Nicholas; Pepke Zaba, Joanna; Toshner, Mark

Shared and Distinct Genomics of Chronic Thromboembolic Pulmonary Hypertension and Pulmonary Embolism. Thumbnail


Authors

Michael Newnham

Marta Bleda

Katherine Bunclark

William Auger

Joan Albert Barbera

Harm Bogaard

Marion Delcroix

Timothy M Fernandes

Luke Howard

David Jenkins

Irene Lang

Eckhard Mayer

Chris Rhodes

Michael Simpson

Laura Southgate

Richard Trembath

John Wharton

Martin R Wilkins

Stefan Gräf

Nicholas Morrell

Joanna Pepke Zaba

Mark Toshner



Abstract

Chronic Thromboembolic Pulmonary Hypertension involves formation and non-resolution of thrombus, dysregulated inflammation, angiogenesis and the development of a small vessel vasculopathy. We aimed to establish the genetic basis of chronic thromboembolic pulmonary hypertension to gain insight into its pathophysiological contributors. We conducted a genome-wide association study on 1907 European cases and 10363 European controls. We co-analysed our results with existing results from genome-wide association studies on deep vein thrombosis, pulmonary embolism and idiopathic pulmonary arterial hypertension. Our primary association study revealed genetic associations at the ABO, FGG, F11, MYH7B, and HLA-DRA loci. Through our co-analysis 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. Chronic thromboembolic pulmonary hypertension is a partially heritable polygenic disease, with related though distinct genetic associations to pulmonary embolism and to deep vein thrombosis.

Citation

Liley, J., Newnham, M., Bleda, M., Bunclark, K., Auger, W., Barbera, J. A., Bogaard, H., Delcroix, M., Fernandes, T. M., Howard, L., Jenkins, D., Lang, I., Mayer, E., Rhodes, C., Simpson, M., Southgate, L., Trembath, R., Wharton, J., Wilkins, M. R., Gräf, S., …Toshner, M. (2024). Shared and Distinct Genomics of Chronic Thromboembolic Pulmonary Hypertension and Pulmonary Embolism. American Journal of Respiratory and Critical Care Medicine, 209(12), 1477-1485. https://doi.org/10.1164/rccm.202307-1236OC

Journal Article Type Article
Acceptance Date Mar 11, 2024
Online Publication Date Mar 17, 2024
Publication Date Jun 15, 2024
Deposit Date May 22, 2024
Publicly Available Date May 22, 2024
Journal American Journal of Respiratory and Critical Care Medicine
Print ISSN 1073-449X
Electronic ISSN 1535-4970
Publisher American Thoracic Society
Peer Reviewed Peer Reviewed
Volume 209
Issue 12
Pages 1477-1485
DOI https://doi.org/10.1164/rccm.202307-1236OC
Keywords Conditional false discovery rate, Pulmonary embolism, Chronic Thromboembolic Pulmonary Hypertension (CTEPH), Pulmonary Hypertension, Genome wide association study
Public URL https://durham-repository.worktribe.com/output/2367013

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