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心室重构中的争议

Controversies in ventricular remodelling.

作者信息

Opie Lionel H, Commerford Patrick J, Gersh Bernard J, Pfeffer Marc A

机构信息

Hatter Institute for Heart Research, Cape Heart Centre and Department of Medicine, University of Cape Town Faculty of Health Sciences, Observatory 7925, Cape Town, South Africa.

出版信息

Lancet. 2006 Jan 28;367(9507):356-67. doi: 10.1016/S0140-6736(06)68074-4.

Abstract

Ventricular remodelling describes structural changes in the left ventricle in response to chronic alterations in loading conditions, with three major patterns: concentric remodelling, when a pressure load leads to growth in cardiomyocyte thickness; eccentric hypertrophy, when a volume load produces myocyte lengthening; and myocardial infarction, an amalgam of patterns in which stretched and dilated infarcted tissue increases left-ventricular volume with a combined volume and pressure load on non-infarcted areas. Whether left-ventricular hypertrophy is adaptive or maladaptive is controversial, as suggested by patterns of signalling pathways, transgenic models, and clinical findings in aortic stenosis. The transition from apparently compensated hypertrophy to the failing heart indicates a changing balance between metalloproteinases and their inhibitors, effects of reactive oxygen species, and death-promoting and profibrotic neurohumoral responses. These processes are evasive therapeutic targets. Here, we discuss potential novel therapies for these disorders, including: sildenafil, an unexpected option for anti-transition therapy; surgery for increased sphericity caused by chronic volume overload of mitral regurgitation; an antifibrotic peptide to inhibit the fibrogenic effects of transforming growth factor beta; mechanical intervention in advanced heart failure; and stem-cell therapy.

摘要

心室重构描述的是左心室结构因长期负荷条件改变而发生的变化,主要有三种模式:向心性重构,即压力负荷导致心肌细胞厚度增加;离心性肥大,即容量负荷使心肌细胞拉长;心肌梗死,是一种多种模式的组合,其中梗死组织的拉伸和扩张会增加左心室容积,并对非梗死区域产生联合的容量和压力负荷。左心室肥大是适应性还是非适应性存在争议,主动脉狭窄中的信号通路模式、转基因模型及临床研究结果表明了这一点。从明显代偿性肥大到心力衰竭的转变表明金属蛋白酶与其抑制剂之间的平衡发生了变化、活性氧的作用以及促死亡和促纤维化的神经体液反应。这些过程是难以捉摸的治疗靶点。在此,我们讨论针对这些病症的潜在新疗法,包括:西地那非,一种用于抗转变治疗的意外选择;针对二尖瓣反流慢性容量超负荷导致的球形度增加的手术;一种抑制转化生长因子β促纤维化作用的抗纤维化肽;晚期心力衰竭的机械干预;以及干细胞治疗。

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