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Pathology and pathobiology of pulmonary hypertension: state of the art and research perspectives

European Respiratory Journal · 2018 · Vol. 53(1) · pp. 1801887–1801887
Marc HumbertChristophe GuignabertSébastien BonnetPeter DorfmüllerJames R. KlingerMark R. NicollsAndrea OlschewskiSoni Savai PullamsettiRalph T. SchermulyKurt R. StenmarkMarlene Rabinovitch

Abstract

Clinical and translational research has played a major role in advancing our understanding of pulmonary hypertension (PH), including pulmonary arterial hypertension and other forms of PH with severe vascular remodelling (<i>e.g.</i> chronic thromboembolic PH and pulmonary veno-occlusive disease). However, PH remains an incurable condition with a high mortality rate, underscoring the need for a better transfer of novel scientific knowledge into healthcare interventions. Herein, we review recent findings in pathology (with the questioning of the strict morphological categorisation of various forms of PH into pre- or post-capillary involvement of pulmonary vessels) and cellular mechanisms contributing to the onset and progression of pulmonary vascular remodelling associated with various forms of PH. We also discuss ways to improve management and to support and optimise drug development in this research field.

Pulmonary Hypertension Research and TreatmentsCardiomyopathy and Myosin StudiesPulmonary hypertensionMedicineChronic thromboembolic pulmonary hypertensionIntensive care medicineVascular remodelling in the embryoPulmonary vasculatureTranslational researchPulmonary pathologyDiseasePsychological intervention

MeSH terms

AnimalsHumansHypertension, PulmonaryMuscle, Smooth, VascularPulmonary ArteryPulmonary VeinsSignal TransductionVascular Remodeling

Funding

  • Pfizer
  • Stanford University
  • United Therapeutics Corporation
  • Janssen Research and Development
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