Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2970951 | The Journal of Heart and Lung Transplantation | 2012 | 6 Pages |
Abstract
The presence of systemic endothelial dysfunction in children with IPAH and its strong association with IPAH severity demonstrate that IPAH is a global vasculopathy. Although morbidity in IPAH is typically associated with pulmonary vascular disease, systemic vascular changes may also relate to disease pathogenesis and progression. Further study into shared mechanisms of systemic and pulmonary endothelial dysfunction may contribute to future therapies for IPAH.
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Authors
Debbie MD, PhD, Jacqueline MD, Miklos MD, Jon A. MD, Jondavid MD, John C. MD, PhD,