[Genetic diagnostics and molecular approaches in pulmonary arterial hypertension]

The recently published new European guidelines for diagnosis and treatment of pulmonary hypertension now offer the so far most extensive description of genetic testing and counselling for pulmonary arterial hypertension patients. In addition, the importance of a clinical screening of healthy mutation carriers is highlighted as well as the genetic testing of patients with a suspicion of pulmonary veno-occlusive disease. We frame the respective parts of the guidelines on genetic testing and counselling in the context of recent data and provide comments. Finally, we give an outlook on novel molecular approaches starting from Sotatercept, addressing ion channels and novel therapeutic developments.

  • Eichstaedt, C. A.
  • Bikou, O.
  • Sommer, N.
  • Schermuly, R. T.
  • Pullamsetti, S. S.
  • Weissmann, N.
  • Harbaum, L.
  • Tabeling, C.
  • Wißmüller, M.
  • Foris, V.
  • Kuebler, W. M.
  • Hinderhofer, K.
  • Olschewski, A.
  • Kwapiszewska, G.

Keywords

  • Humans
  • *Pulmonary Arterial Hypertension
  • Familial Primary Pulmonary Hypertension/diagnosis/genetics/therapy
  • *Hypertension, Pulmonary/diagnosis/genetics/therapy
  • *Pulmonary Veno-Occlusive Disease/diagnosis/genetics/therapy
Publication details
DOI: 10.1055/a-2145-4663
Journal: Pneumologie
Pages: 862-870
Number: 11
Work Type: Original
Access number: 37963476
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