نتایج جستجو برای: ipah

تعداد نتایج: 494  

Journal: :FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2007
Hemal H Patel Shen Zhang Fiona Murray Ryan Y S Suda Brian P Head Utako Yokoyama James S Swaney Ingrid R Niesman Ralph T Schermuly Soni Savai Pullamsetti Patricia A Thistlethwaite Atsushi Miyanohara Marilyn G Farquhar Jason X-J Yuan Paul A Insel

Vasoconstriction and vascular medial hypertrophy, resulting from increased intracellular [Ca2+] in pulmonary artery smooth muscle cells (PASMC), contribute to elevated vascular resistance in patients with idiopathic pulmonary arterial hypertension (IPAH). Caveolae, microdomains within the plasma membrane, contain the protein caveolin, which binds certain signaling molecules. We tested the hypot...

Journal: :European journal of immunology 2018
Lisa K Blum Richard R L Cao Andrew J Sweatt Matthew Bill Lauren J Lahey Andrew C Hsi Casey S Lee Sarah Kongpachith Chia-Hsin Ju Rong Mao Heidi H Wong Mark R Nicolls Roham T Zamanian William H Robinson

Idiopathic pulmonary arterial hypertension (IPAH) is a devastating pulmonary vascular disease in which autoimmune and inflammatory phenomena are implicated. B cells and autoantibodies have been associated with IPAH and identified as potential therapeutic targets. However, the specific populations of B cells involved and their roles in disease pathogenesis are not clearly defined. We aimed to as...

Journal: :American journal of physiology. Lung cellular and molecular physiology 2007
Fares A Masri Weiling Xu Suzy A A Comhair Kewal Asosingh Michelle Koo Amit Vasanji Judith Drazba Bela Anand-Apte Serpil C Erzurum

Idiopathic pulmonary arterial hypertension (IPAH) is characterized by plexiform vascular lesions, which are hypothesized to arise from deregulated growth of pulmonary artery endothelial cells (PAEC). Here, functional and molecular differences among PAEC derived from IPAH and control human lungs were evaluated. Compared with control cells, IPAH PAEC had greater cell numbers in response to growth...

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...

Journal: :Respiratory Research 2006
Alasdair J Edgar Matilde R Chacón Anne E Bishop Magdi H Yacoub Julia M Polak

BACKGROUND To elucidate further the pathogenesis of sporadic, idiopathic pulmonary arterial hypertension (IPAH) and identify potential therapeutic avenues, differential gene expression in IPAH was examined by suppression subtractive hybridisation (SSH). METHODS Peripheral lung samples were obtained immediately after removal from patients undergoing lung transplant for IPAH without familial di...

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: :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...

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