نتایج جستجو برای: ipah gene

تعداد نتایج: 1141692  

2014
J. K. Mansoor Edward S. Schelegle Cristina E. Davis William F. Walby Weixiang Zhao Alexander A. Aksenov Alberto Pasamontes Jennifer Figueroa Roblee Allen

BACKGROUND An important challenge to pulmonary arterial hypertension (PAH) diagnosis and treatment is early detection of occult pulmonary vascular pathology. Symptoms are frequently confused with other disease entities that lead to inappropriate interventions and allow for progression to advanced states of disease. There is a significant need to develop new markers for early disease detection a...

Journal: :The European respiratory journal 2009
M J Overbeek M C Vonk A Boonstra A E Voskuyl A Vonk-Noordegraaf E F Smit B A C Dijkmans P E Postmus W J Mooi Y Heijdra K Grünberg

Systemic sclerosis-associated pulmonary arterial hypertension (SScPAH) has a worse prognosis and response to pulmonary arterial hypertension (PAH) therapy than idiopathic PAH (IPAH). These differences have not yet been explained. Knowledge concerning histological pulmonary vasculopathy in SScPAH is limited in contrast to IPAH. Therefore, we explored patterns of vasculopathy in SScPAH compared w...

2016
Lars Harbaum Emilia Renk Sara Yousef Antonia Glatzel Nicole Lüneburg Jan K. Hennigs Tim Oqueka Hans J. Baumann Djordje Atanackovic Ekkehard Grünig Rainer H. Böger Carsten Bokemeyer Hans Klose

BACKGROUND Exercise training positively influences exercise tolerance and functional capacity of patients with idiopathic pulmonary arterial hypertension (IPAH). However, the underlying mechanisms are unclear. We hypothesized that exercise modulates the activated inflammatory state found in IPAH patients. METHODS Single cardiopulmonary exercise testing was performed in 16 IPAH patients and 10...

Journal: :Thorax 2009
S Hall P Brogan S G Haworth N Klein

Idiopathic pulmonary arterial hypertension (IPAH) is an incurable disease of multifactorial origin. Inflammation is frequently observed in IPAH, but its role in the pathobiology is unclear. In this study the distribution, nature and number of inflammatory cells in periarterial infiltrates in lungs of children with IPAH, pulmonary arterial hypertension associated with congenital heart disease (A...

Journal: :American journal of physiology. Lung cellular and molecular physiology 2016
Haiyang Tang Aya Yamamura Hisao Yamamura Shanshan Song Dustin R Fraidenburg Jiwang Chen Yali Gu Nicole M Pohl Tong Zhou Laura Jiménez-Pérez Ramon J Ayon Ankit A Desai David Goltzman Franz Rischard Zain Khalpey Stephan M Black Joe G N Garcia Ayako Makino Jason X J Yuan

An increase in cytosolic free Ca(2+) concentration ([Ca(2+)]cyt) in pulmonary arterial smooth muscle cells (PASMC) is a major trigger for pulmonary vasoconstriction and a critical stimulation for PASMC proliferation and migration. Previously, we demonstrated that expression and function of calcium sensing receptors (CaSR) in PASMC from patients with idiopathic pulmonary arterial hypertension (I...

Journal: :Journal of the American College of Cardiology 2016
Christian F Opitz Marius M Hoeper J Simon R Gibbs Harald Kaemmerer Joanna Pepke-Zaba J Gerry Coghlan Laura Scelsi Michele D'Alto Karen M Olsson Silvia Ulrich Werner Scholtz Uwe Schulz Ekkehard Grünig Carmine D Vizza Gerd Staehler Leonhard Bruch Doerte Huscher David Pittrow Stephan Rosenkranz

BACKGROUND Pulmonary hypertension (PH) is hemodynamically classified as pre-capillary (as seen in idiopathic pulmonary arterial hypertension [IPAH]) or post-capillary (as seen in heart failure with preserved ejection fraction [HFpEF]). Overlaps between these conditions exist. Some patients present with risk factors for left heart disease but pre-capillary PH, whereas patients with HFpEF may hav...

2012
Kayoko Shimodaira Yoichiro Okubo Eri Ochiai Haruo Nakayama Harutaka Katano Megumi Wakayama Minoru Shinozaki Takao Ishiwatari Daisuke Sasai Naobumi Tochigi Tetsuo Nemoto Tsutomu Saji Katsuhiko Kamei Kazutoshi Shibuya

BACKGROUND Idiopathic pulmonary arterial hypertension (IPAH) continues to be one of the most serious intractable diseases that might start with activation of several triggers representing the genetic susceptibility of a patient. To elucidate what essentially contributes to the onset and progression of IPAH, we investigated factors playing an important role in IPAH by searching discrepant or con...

2006
Shen Zhang Hemal H. Patel Fiona Murray Carmelle V. Remillard Christian Schach Patricia A. Thistlethwaite Paul. A. Insel Jason X.-J. Yuan Paul A. Insel

Pulmonary vascular remodeling due to overgrowth of pulmonary artery smooth muscle cells (PASMC) is a major cause for the elevated vascular resistance in patients with idiopathic pulmonary arterial hypertension (IPAH). Increased cytosolic Ca ([Ca]cyt), resulting from enhanced capacitative Ca entry (CCE) and upregulated transient receptor potential (TRP) channel expression, is involved in stimula...

2016
Mieke M. P. Driessen Wei Hui Bart H. Bijnens Andreea Dragulescu Luc Mertens Folkert J. Meijboom Mark K. Friedberg

Right ventricular (RV) pressure overload has a vastly different clinical course in children with idiopathic pulmonary arterial hypertension (iPAH) than in children with pulmonary stenosis (PS). While RV function is well recognized as a key prognostic factor in iPAH, adverse ventricular-ventricular interactions and LV dysfunction are less well characterized and the pathophysiology is incompletel...

Journal: :Respiration; international review of thoracic diseases 2010
Silvia Ulrich Justyna Szamalek-Hoegel Martin Hersberger Manuel Fischler Jesus Solera Garcia Lars C Huber Ekkehard Grünig Bart Janssen Rudolf Speich

BACKGROUND Idiopathic pulmonary arterial hypertension (IPAH) and chronic thromboembolic pulmonary hypertension (CTEPH) share important pathogenic and clinical features. BMPR2 mutations are important in the pathogenesis of IPAH, but little is known about the genetic background in CTEPH. OBJECTIVE To search for mutations and polymorphisms in genes involved in the BMPR2, serotonin and nitric oxi...

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