Heritable pulmonary arterial hypertension: new genetic findings and environmental triggers

Our goal was to identify new environmental or genetic causes in heritable pulmonary arterial hypertension (HPAH) families outside the 18 known diagnostics PAH genes. PAH gene panel sequencing was performed for 47 HPAH families which revealed pathogenic variants in 39 families. Five of the remaining families agreed to whole exome sequencing and to fill in a drug and toxin exposure questionnaire. In Family 1 and 2, mother and daughter with HPAH carried a likely pathogenic variant in the CYBA gene and a variant of uncertain significance in the FKBP1A gene, respectively, following ACMG guidelines. In Family 3, we detected a likely pathogenic variant in the PTGR2 gene. These genes could play part in PAH pathogenesis but further functional analyses are required to corroborate these findings. In the remaining two families, we could not identify any plausible genetic cause. However, a father and son with PAH reported exposure to trichloroethylene, asbestos and tramadol in Family 4. In Family 5, two brothers with pulmonary veno-occlusive disease showed occupational toxin exposure. Thus, our findings indicate that not only a genetic predisposition but also environmental triggers should be investigated for HPAH patients.

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Publication Details

Journal
Scientific Reports
Published
2026-01-29
DOI
https://doi.org/10.1038/s41598-025-34167-0
Primary Topic
Pulmonary Hypertension Research and Treatments
Type
article
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article

Heritable pulmonary arterial hypertension: new genetic findings and environmental triggers

Jan Haas, Peter Dorfmüller, Satenik Harutyunova, Natascha Sommer et al.
Scientific Reports
Pulmonary Hypertension Research and Treatments
article

Heritable pulmonary arterial hypertension: new genetic findings and environmental triggers

Jan Haas, Peter Dorfmüller, Satenik Harutyunova, Natascha Sommer, Martin Granzow, Katrin Hinderhofer, Ekkehard Grünig, Memoona Shaukat, Tobias J. Lange, Benjamin Egenlauf, Mohammad Panahi, Benjamin Meder, Christina A. Eichstaedt, Simon Haas, Panagiota Xanthouli, Stefan Stadler
article en

Abstract

Our goal was to identify new environmental or genetic causes in heritable pulmonary arterial hypertension (HPAH) families outside the 18 known diagnostics PAH genes. PAH gene panel sequencing was performed for 47 HPAH families which revealed pathogenic variants in 39 families. Five of the remaining families agreed to whole exome sequencing and to fill in a drug and toxin exposure questionnaire. In Family 1 and 2, mother and daughter with HPAH carried a likely pathogenic variant in the CYBA gene and a variant of uncertain significance in the FKBP1A gene, respectively, following ACMG guidelines. In Family 3, we detected a likely pathogenic variant in the PTGR2 gene. These genes could play part in PAH pathogenesis but further functional analyses are required to corroborate these findings. In the remaining two families, we could not identify any plausible genetic cause. However, a father and son with PAH reported exposure to trichloroethylene, asbestos and tramadol in Family 4. In Family 5, two brothers with pulmonary veno-occlusive disease showed occupational toxin exposure. Thus, our findings indicate that not only a genetic predisposition but also environmental triggers should be investigated for HPAH patients.

Scientific ReportsVol. 16(1)
Heidelberg University (DE), University Hospital Heidelberg (DE), Institute of Human Genetics (PL), German Centre for Cardiovascular Research (DE), German Center for Lung Research (DE), Universities of Giessen and Marburg Lung Center (DE), Klinik Bad Reichenhall (DE), Cardio-Pulmonary Institute (DE)
Openalex Percentile: Top 75%
Pulmonary Hypertension Research and Treatments
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