Pulmonary hypertension: advances in pathogenesis and treatment

被引:19
作者
Toshner, M. [1 ]
Tajsic, T. [1 ]
Morrell, N. W. [1 ]
机构
[1] Univ Cambridge, Dept Med, Cambridge CB2 2QQ, England
关键词
pulmonary hypertension; vascular remodelling; ENDOTHELIAL PROGENITOR CELLS; SOLUBLE GUANYLATE-CYCLASE; CALCIUM-CHANNEL BLOCKERS; ARTERIAL-HYPERTENSION; TENASCIN-C; GERMLINE MUTATIONS; GENE-THERAPY; HYPOXIA; LUNG; TRANSPLANTATION;
D O I
10.1093/bmb/ldq012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pulmonary hypertension is an orphan disease that until recently has received limited attention within the wider medical community. This has changed distinctly in the last 10 years with the advent of new classes of therapy and a renewed interest in mechanisms of pathogenesis. This review utilized information gathered from recent conferences, and a review of the literature was conducted using MedLine and Pubmed. Accepted mechanisms of pathogenesis and currently available treatments are presented. We will discuss interesting new concepts in pathogenesis, including the importance of genetic forms of the disease and in particular the transforming growth factor receptor superfamily and the evolving evidence of the contribution of dysregulated immunity. Areas of research may yield therapeutic benefits in the not-too-distant future, including anti-proliferative therapies and stem cell therapy.
引用
收藏
页码:21 / 32
页数:12
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