Zobrazeno 1 - 10
of 1 361
pro vyhledávání: '"idiopathic pulmonary arterial hypertension"'
Autor:
Sicheng Zhang, Sicong Li, Luyang Gao, Qing Zhao, Tao Yang, Qixian Zeng, Zhihua Huang, Xin Li, Anqi Duan, Yijia Wang, Zhihui Zhao, Qin Luo, Zhihong Liu
Publikováno v:
Respiratory Research, Vol 25, Iss 1, Pp 1-12 (2024)
Abstract Background Malnutrition is common in patients with chronic cardiovascular disease and is associated with significantly higher all-cause mortality. Approximately one-third of patients with heart failure are malnourished. However, the relation
Externí odkaz:
https://doaj.org/article/ae92e8a344784455a8418adaf8cfc65b
Autor:
Sicheng Zhang, Luyang Gao, Sicong Li, Manqing Luo, Lichuan Chen, Qunying Xi, Zhihui Zhao, Qing Zhao, Tao Yang, Qixian Zeng, Xin Li, Zhihua Huang, Anqi Duan, Yijia Wang, Qin Luo, Yansong Guo, Zhihong Liu
Publikováno v:
Cardiovascular Diabetology, Vol 23, Iss 1, Pp 1-15 (2024)
Abstract Background Insulin resistance (IR) plays an important role in the pathophysiology of cardiovascular disease. Recent studies have shown that diabetes mellitus and impaired lipid metabolism are associated with the severity and prognosis of idi
Externí odkaz:
https://doaj.org/article/71cd9bea5308487688425eac96068108
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Objective This study aimed to investigate the serum levels of Peptidase M20 domain containing 1 (PM20D1) in idiopathic pulmonary arterial hypertension (IPAH) patients and examine its association with lipid metabolism, echocardiography, and h
Externí odkaz:
https://doaj.org/article/67efca1853a54d5cb09c6588b98f9faf
Autor:
Reda E. Girgis, Nabin K. Manandhar‐Shrestha, Sheila Krishnan, Edward T. Murphy, Renzo Loyaga‐Rendon
Publikováno v:
Pulmonary Circulation, Vol 14, Iss 2, Pp n/a-n/a (2024)
Abstract Lung transplantation remains an important therapeutic option for idiopathic pulmonary arterial hypertension (IPAH), yet short‐term survival is the poorest among the major diagnostic categories. We sought to develop a prediction model for 9
Externí odkaz:
https://doaj.org/article/cfcd5541830d4ebb869625b3b1d1b6c5
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Idiopathic pulmonary arterial hypertension (IPAH) is a rare and severe cardiopulmonary disease with a challenging prognosis, and its underlying pathogenesis remains elusive. A comprehensive understanding of IPAH is crucial to unveil potential diagnos
Externí odkaz:
https://doaj.org/article/cd551b4008fd4cfc8d3414992f47657d
Autor:
André Alexandre, Inês Furtado, Luísa Carvalho, Fabienne Gonçalves, Alzira Melo, Joana Alves, Mário Santos, Abílio Reis
Publikováno v:
ESC Heart Failure, Vol 10, Iss 4, Pp 2722-2727 (2023)
Abstract Intravenous (i.v.) prostacyclin is the cornerstone treatment in high‐risk pulmonary arterial hypertension (PAH) patients. Selexipag is an orally available prostacyclin receptor agonist. Limited data are available regarding the feasibility
Externí odkaz:
https://doaj.org/article/9a2e62bd3b1d4fdf97f8b421e65c0ea8
Autor:
Hui Zhao, Ruowang Duan, Qian Wang, Xiaoyi Hu, Qinhua Zhao, Wenhui Wu, Rong Jiang, Sugang Gong, Lan Wang, Jinming Liu, Jie Deng, Huazheng Liang, Yuqing Miao, Ping Yuan
Publikováno v:
Heliyon, Vol 9, Iss 12, Pp e22922- (2023)
MicroRNAs (miRNAs) are versatile regulators of pulmonary arterial remodeling in idiopathic pulmonary arterial hypertension (IPAH). We herein aimed to characterize miRNAs in peripheral blood mononuclear cell (PBMC) and plasma exosomes, and investigate
Externí odkaz:
https://doaj.org/article/face7c9cc78d45d399ef44468e76553f
Autor:
Ting Huang, Yunhong Zeng, Yao Yang, Haoqin Fan, Youcai Deng, Wenjuan Chen, Jinqiao Liu, Fan Yang, Wenfeng Li, Yunbin Xiao
Publikováno v:
Epigenetics, Vol 18, Iss 1 (2023)
Idiopathic pulmonary arterial hypertension (IPAH) is a serious and fatal disease. Recently, m6A has been reported to play an important role in the lungs of IPAH patients and experimental pulmonary hypertension models. However, the meaning of m6A mRNA
Externí odkaz:
https://doaj.org/article/9fd0b8ca7cb741f3b7c45a4c18c43b48
Autor:
Mithilesh Kulkarni, Dinesh Joshi, Karthik Natrajan, Vishal Sharma, Sharad Jain, Riyaz Charaniya, Pooja Vyas, Krutika Patel, Gunjan Shah, Nisarg Desai
Publikováno v:
Heart India, Vol 11, Iss 3, Pp 113-118 (2023)
Context: Pulmonary hypertension (PH) is a condition characterized by an increase in pulmonary artery pressure, leading to morbidity and poor survival. In India, the high prevalence of certain diseases contributes to the burden of PH. To address this,
Externí odkaz:
https://doaj.org/article/1f8bbc2713384e1a85060796a5411e40
Autor:
Natalia Goncharova, Kirill Lapshin, Aelita Berezina, Maria Simakova, Alexandr Marichev, Irina Zlobina, Narek Marukyan, Kirill Malikov, Alexandra Aseeva, Vadim Zaitsev, Olga Moiseeva
Publikováno v:
Life, Vol 14, Iss 2, p 259 (2024)
Introduction: The predictive value of the risk stratification scales in elderly patients with IPAH might differ from that in younger patients. It is unknown whether young and older IPAH patients have the same survival dependence on PAH-specific thera
Externí odkaz:
https://doaj.org/article/83c7fc453f504dc491c8dbc7fd9d49cb