| Literature DB >> 19555854 |
Hossein A Ghofrani1, Robyn J Barst2, Raymond L Benza3, Hunter C Champion4, Karen A Fagan5, Friedrich Grimminger6, Marc Humbert7, Gérald Simonneau7, Duncan J Stewart8, Carlo Ventura9, Lewis J Rubin10.
Abstract
Over the past 2 decades, pulmonary arterial hypertension has evolved from a uniformly fatal condition to a chronic, manageable disease in many cases, the result of unparalleled development of new therapies and advances in early diagnosis. However, none of the currently available therapies is curative, so the search for new treatment strategies continues. With a deeper understanding of the genetics and the molecular mechanisms of pulmonary vascular disorders, we are now at the threshold of entering a new therapeutic era. Our working group addressed what can be expected in the near future. The topics span the understanding of genetic variations, novel antiproliferative treatments, the role of stem cells, the right ventricle as a therapeutic target, and strategies and challenges for the translation of novel experimental findings into clinical practice.Entities:
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Year: 2009 PMID: 19555854 PMCID: PMC4883573 DOI: 10.1016/j.jacc.2009.04.014
Source DB: PubMed Journal: J Am Coll Cardiol ISSN: 0735-1097 Impact factor: 24.094