نتایج جستجو برای: ژن ipah

تعداد نتایج: 16248  

Journal: :American journal of physiology. Lung cellular and molecular physiology 2011
Metin Aytekin Raed A Dweik

TO THE EDITOR: We read with interest the article by Ormiston et al. (2) “The enzymatic degradation of hyaluronan is associated with disease progression in experimental pulmonary hypertension” and wish to make a few comments. In Ormiston and colleagues’ interpretation of our study, they accurately described the increased levels of hyaluronan (HA) we reported in pulmonary artery smooth muscle cel...

Journal: :American journal of respiratory and critical care medicine 2006
Laurence Dewachter Serge Adnot Elie Fadel Marc Humbert Bernard Maitre Anne-Marie Barlier-Mur Gerald Simonneau Michel Hamon Robert Naeije Saadia Eddahibi

RATIONALE Angiopoietins are involved in blood vessel maturation and remodeling. OBJECTIVES One consequence of endothelium-specific tyrosine kinase-2 (Tie2) receptor activation by angiopoietin-1 (Ang1) is the release of endothelium-derived growth factors that recruit vascular wall cells. We investigated this process in idiopathic pulmonary arterial hypertension (iPAH). METHODS Ang1, Ang2, an...

2006
Laurence Dewachter Serge Adnot Elie Fadel Marc Humbert Bernard Maitre Anne-Marie Barlier-Mur Gerald Simonneau Michel Hamon Robert Naeije Saadia Eddahibi

Rationale: Angiopoietins are involved in blood-vessel maturation and remodeling. Objectives: One consequence of endothelial-specific receptor Tie2 activation by angiopoietin-1 (Ang1) is the release of endothelial-derived growth factors that recruit vascular wall cells. We investigated this process in idiopathic pulmonary arterial hypertension (iPAH). Methods: Ang1, Ang2, total and phosphorylate...

2013
ABDULLAH S. ASSIRI

Objectives: To characterize the demographic and clinical profiles of patients with Idiopathic Pulmonary Arterial Hypertension (IPAH) admitted to the tertiary care hospital in Aseer region, and to evaluate the altitude effect. Design: A retrospective cohort study. Setting: Aseer Central Hospital. Subjects: All patients admitted with the diagnosis of (IPAH) during the period from January 2001 to ...

2014
Xiaoyue Tan Wenlan Yang Jian Guo Yan Zhang Changwei Wu Rikesh Sapkota Shailendra Prasad Kushwaha Sugang Gong Xingguo Sun Jinming Liu

BACKGROUND Decline in oxygen uptake efficiency (OUE), especially during exercise, is found in patients with chronic heart failure. In this study we aimed to test the validity and usefulness of OUE in evaluating gas exchange abnormality of patients with idiopathic pulmonary arterial hypertension (IPAH). METHODS We retrospectively investigated the cardiopulmonary exercise test (CPET) with gas e...

Journal: :Archivos de cardiologia de Mexico 2011
Eulo Lupi-Herrera Julio Sandoval Javier Figueroa Arturo Carrillo Rebeca Aguirre Luis Efren Santos-Martínez Tomás Pulido

INTRODUCTION Despite the prognostic importance of traditionally derived measurements, the significance of right heart catheterization (RHC) remains controversial. Thus, a continued search for hemodynamic markers that define better responsive patients is required. Since, right ventricular failure is the most fatal pathway, right (RVPO) and left (LVPO) ventricular power output are parameters that...

2011
Livia Kapusta

Background—Incidence and prevalence rates for pediatric pulmonary hypertension (PH) and pulmonary arterial hypertension (PAH) are unknown. This study describes the nationwide epidemiological features of pediatric PH in the Netherlands during a 15-year period and the clinical course of pediatric PAH. Methods and Results—Two registries were used to retrospectively identify children (0–17 years) w...

2011
Michael Y. Song Ayako Makino Jason X.-J. Yuan

Pulmonary vasoconstriction and vascular remodeling are two major causes for elevated pulmonary vascular resistance and pulmonary arterial pressure in patients with idiopathic pulmonary arterial hypertension (IPAH). An increase in cytosolic free Ca(2+) concentration ([Ca(2+)](cyt)) in pulmonary artery smooth muscle cells (PASMC) is a major trigger for pulmonary vasoconstriction and an important ...

Journal: :European journal of heart failure 2011
Yeun Ying Wong Nico Westerhof Gerrina Ruiter Mark Lubberink Pieter Raijmakers Paul Knaapen J Tim Marcus Anco Boonstra Adriaan A Lammertsma Willem J van der Laarse Anton Vonk-Noordegraaf

AIMS Increased afterload in idiopathic pulmonary arterial hypertension (IPAH) causes right ventricular (RV) hypertrophy and failure. Since RV remodelling occurs with alterations in RV oxygen metabolism, increasing our understanding in the factors determining RV O(2) consumption in IPAH is necessary. In the left ventricle, it is known that heart rate and systolic blood pressure are the main dete...

Journal: :ERJ Open Research 2021

Despite systematic screening and improved treatment strategies, the prognosis remains worse in patients with connective tissue disease-associated pulmonary arterial hypertension (CTD-PAH) compared to idiopathic/hereditary (IPAH). We aimed investigate differences clinical characteristics, outcome, performance of ESC/ERS risk stratification tool these patient groups. This retrospective analysis i...

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