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[扩张型心肌病的发病机制:一项基于临床特征与其他相关病症比较的研究]

[Pathogenesis of dilated cardiomyopathy: a study based on comparison of the clinical features with other related conditions].

作者信息

Takarada A, Yokota Y, Seo T, Maehashi N, Kubo M, Nakanishi O, Teng S S, Masuda J, Fukuzaki H

机构信息

First Department of Internal Medicine, Kobe University School of Medicine.

出版信息

J Cardiol. 1987 Mar;17(1):57-64.

PMID:3429922
Abstract

To investigate the pathogenesis and pathophysiology of dilated cardiomyopathy (DCM), we studied 28 patients with DCM by echocardiography and endomyocardial biopsy, and compared their findings with those of 34 patients including eight with myocarditis, seven with alcoholics, 12 with hypertensives and seven patients with hypertrophic cardiomyopathy. All 12 patients in the hypertensive group had congestive heart failure without accompanying high blood pressure, and prominent dilatation and uniform wall motion abnormality of the left ventricle observed echocardiographically on admission. After medical management, both heart failure and the echocardiographic abnormalities gradually resolved. Those in the alcoholic group had larger left ventricles and uniform wall motion abnormality compared to those in the other groups. The myocarditis and hypertrophic cardiomyopathy groups had smaller left ventricles, non-uniform wall motion and larger % myocardial fibrosis. Both ventricles in the hypertrophic cardiomyopathy group were thicker than those of the other three groups. Each patient with DCM had individual echocardiographic abnormalities, which could be categorized as two subsets depending on the degree of left ventricular dilatation and uniformity of the wall motion. The one was characterized by a prominently dilated left ventricle and uniform wall motion abnormality similar to the alcoholic group, and the other had less marked left ventricular dilatation and heterogeneous wall motion abnormality similar to the myocarditis group. From these findings, it was suggested that there are common factors to specific myocardial disease in the pathogenesis and pathophysiology of DCM, and thus, DCM might include many subsets of different etiologies.

摘要

为了研究扩张型心肌病(DCM)的发病机制和病理生理学,我们通过超声心动图和心内膜心肌活检对28例DCM患者进行了研究,并将他们的检查结果与34例患者的结果进行了比较,这34例患者包括8例心肌炎患者、7例酒精性心肌病患者、12例高血压性心脏病患者和7例肥厚型心肌病患者。高血压组的所有12例患者均患有充血性心力衰竭且无高血压伴发,入院时超声心动图观察到左心室显著扩张和均匀的室壁运动异常。经过药物治疗后,心力衰竭和超声心动图异常均逐渐缓解。与其他组相比,酒精性心肌病组患者的左心室更大且室壁运动均匀异常。心肌炎组和肥厚型心肌病组患者的左心室较小,室壁运动不均匀且心肌纤维化百分比更高。肥厚型心肌病组患者的两个心室均比其他三组更厚。每位DCM患者都有各自的超声心动图异常,根据左心室扩张程度和室壁运动的均匀性可将其分为两个亚组。一组的特征是左心室显著扩张且室壁运动均匀异常,类似于酒精性心肌病组;另一组左心室扩张不明显且室壁运动不均一异常,类似于心肌炎组。从这些发现可以看出,在DCM的发病机制和病理生理学中存在特定心肌疾病的共同因素,因此,DCM可能包括许多不同病因的亚组。

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