News

Study Shows That Reducing Inflammasome Proteins Reduces PH in Mice

The inflammasome, which is a multi-protein complex that activates inflammatory processes, was shown to play a role in pulmonary hypertension according to a journal article from the Institute for Experimental Medical Research in Oslo University Hospital. Removing a key component of the inflammasome in mice predisposed to pulmonary hypertension were rescued…

Mayo Clinic and United Therapeutics Collaborate on Lung Restoration Center

The Mayo Clinic’s Jacksonville, Florida unit and Silver Spring, Maryland-based biotechnology company United Therapeutics Corporation have announced that they will collaborate on construction and operation of a lung restoration center to be located on Mayo’s Jacksonville campus. The project’s goal is to significantly increase the volume of lungs…

Autoantibodies Targeted in New Strategy to Treat IPF

Novel research investigating the relationship between autoantibodies and idiopathic pulmonary fibrosis (IPF) may allow new therapies to be developed based on current treatments for autoimmune diseases. The laboratory of Steve Duncan, MD, at the University of Alabama at Birmingham Division of Pulmonary, Allergy, and Critical Care Medicine recently published a study…

Therapy Targeting Specific Mutation Reverses PAH in Mice

Targeting a mutation common to 15-40% of cases of idiopathic pulmonary arterial hypertension (PAH) with a specific drug target may help cure heritable forms of PAH. A study from Dr. Nicholas W. Morrell’s laboratory at the University of Cambridge reversed the signs of PAH in mice treated with bone-morphogenetic protein…

Diagnosis, Non-Surgical Treatments For CTEPH Gaining Ground

Understanding the science behind chronic thromboembolic pulmonary hypertension (CTEPH) has come a long way since, originally, a diagnosis was made postmortem. Although it is commonly underdiagnosed and undertreated, CTEPH can be cured via pulmonary endarterectomy (PEA), a technique that dates back almost to the first diagnosis of CTEPH. “At the…

Genetic Defects Found To Potentially Lead to PAH, Endothelium Injury

When exploring the origins of pulmonary arterial hypertension, researchers regard injuries to the endothelium of blood vessels as an important factor leading to the development of the disease, as remodeling in the pulmonary vessels can lead to increased pressure and resistance in the arteries. In order to address endothelium injury and create new…

Nine New Pulmonary Hypertension Care Centers Accredited By PHA

The Pulmonary Hypertension Association (PHA) recently announced the accreditation of nine new institutions as established Pulmonary Hypertension Care Centers (PHCC). The granting of this status recognizes excellency and specialization in the treatment of patients with pulmonary hypertension (PH), and the addition of nine more PHCC expands the…

Experimental PH Therapies Now Focusing on Treating Pathological Pulmonary Arterial Smooth Muscle Cells

As more scientific studies are conducted to understand pulmonary hypertension, it is becoming more apparent that pulmonary arterial smooth muscle cells (PASMCs) are important to the pathology of pulmonary hypertension. A group of researchers at the Pittsburgh Heart, Lung, Blood, and Vascular Medicine Institute recently reported on the advances in therapies…