Department of Pathology and Matrix Biology, Mie University Graduate School of Medicine, Mie, Japan.
Mie University Research Center for Matrix Biology, Mie, Japan.
Pathol Int. 2020 Jan;70(1):1-11. doi: 10.1111/pin.12868. Epub 2019 Nov 5.
Dilated cardiomyopathy (DCM) is a heterogeneous group of myocardial diseases clinically defined by the presence of left ventricular dilatation and contractile dysfunction. Among various causes of DCM, a progression from viral myocarditis to DCM has long been hypothesized. Supporting this possibility, studies by endomyocardial biopsy, the only method to obtain a definite diagnosis of myocarditis at present, have provided evidence of inflammation in the myocardium in DCM patients. A number of experimental studies have elucidated a cell-mediated autoimmune mechanism triggered by viral infection in the progression of myocarditis to DCM. In addition, the important role of inflammation in the pathogenesis of heart failure has been recognized, and many terms including myocarditis, inflammatory cardiomyopathy, and inflammatory DCM have been used for myocardial diseases associated with inflammation. This review discusses the pathophysiology of inflammation in the myocardium, and refers to diagnosis and treatment based on these concepts.
扩张型心肌病(DCM)是一组心肌疾病,临床上以左心室扩张和收缩功能障碍为特征。在 DCM 的各种病因中,病毒心肌炎向 DCM 进展的假说由来已久。支持这种可能性的是,通过心内膜心肌活检(目前获得心肌炎明确诊断的唯一方法)进行的研究提供了 DCM 患者心肌炎症的证据。许多实验研究阐明了病毒感染引发的细胞介导自身免疫机制在心肌炎向 DCM 进展中的作用。此外,炎症在心力衰竭发病机制中的重要作用已得到认可,许多术语,如心肌炎、炎症性心肌病和炎症性 DCM,已被用于与炎症相关的心肌疾病。本文讨论了心肌炎症的病理生理学,并参考了基于这些概念的诊断和治疗方法。