Evidence for Right Ventricular Lipotoxicity in Heritable Pulmonary Arterial Hypertension

Rationale: Shorter survival in heritable pulmonary arterial hypertension (HPAH), often due to BMPR2 mutation, has been described in association with impaired right ventricle (RV) compensation. HPAH animal models are insulin resistant, and cells with BMPR2 mutation have impaired fatty acid oxidation,...

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Détails bibliographiques
Auteurs principaux: Hemnes, Anna R., Brittain, Evan L., Trammell, Aaron W., Fessel, Joshua P., Austin, Eric D., Penner, Niki, Maynard, Karen B., Gleaves, Linda, Talati, Megha, Absi, Tarek, DiSalvo, Thomas, West, James
Format: Artigo
Langue:Inglês
Publié: American Thoracic Society 2014
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Original Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3977729/
https://ncbi.nlm.nih.gov/pubmed/24274756
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201306-1086OC
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