共 50 条
Group 3 Pulmonary Hypertension: From Bench to Bedside
被引:40
|作者:
Singh, Navneet
[1
]
Dorfmuller, Peter
[3
,4
,5
]
Shlobin, Oksana A.
[6
]
Ventetuolo, Corey E.
[1
,2
]
机构:
[1] Brown Univ, Div Pulm Crit Care & Sleep Med, 593 Eddy St,APC 757, Providence, RI 02903 USA
[2] Brown Univ, Dept Hlth Serv Policy & Practice, Providence, RI USA
[3] Univ Giessen, Dept Pathol, Giessen, Germany
[4] Justus Liebig Univ, Marburg Lung Ctr UGMLC, Giessen, Germany
[5] German Ctr Lung Res DZL, Giessen, Germany
[6] Inova Fairfax Hosp, Adv Lung Dis & Transplant Program, Falls Church, VA USA
关键词:
hypertension;
pulmonary;
hypoxia;
lung diseases;
interstitial;
prevalence;
ventricular dysfunction;
right;
INHALED NITRIC-OXIDE;
ENDOTHELIAL GROWTH-FACTOR;
RIGHT-VENTRICULAR DYSFUNCTION;
BRAIN NATRIURETIC PEPTIDE;
INTERSTITIAL LUNG-DISEASE;
SMOKE-INDUCED EMPHYSEMA;
TERM OXYGEN-THERAPY;
6-MINUTE WALK TEST;
ANIMAL-MODELS;
ARTERIAL-HYPERTENSION;
D O I:
10.1161/CIRCRESAHA.121.319970
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Pulmonary hypertension (PH) because of chronic lung disease is categorized as Group 3 PH in the most recent classification system. Prevalence of these diseases is increasing over time, creating a growing need for effective therapeutic options. Recent approval of the first pulmonary arterial hypertension therapy for the treatment of Group 3 PH related to interstitial lung disease represents an encouraging advancement. This review focuses on molecular mechanisms contributing to pulmonary vasculopathy in chronic hypoxia, the pathology and epidemiology of Group 3 PH, the right ventricular dysfunction observed in this population and clinical trial data that inform the use of pulmonary vasodilators in Group 3 PH.
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页码:1404 / 1422
页数:19
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