Dilated cardiomyopathy as a clinical model of premature aging in humans

Abstract

The compliance of dilated cardiomyopathy (DCM) with the requirements of a clinical model of premature aging in humans is substantiated. The pathogenetic basis of the formation of DCM and their relationship with changes associated with myocardial aging are considered. The study complements and clarifies the understanding of the pathogenetic mechanisms of premature aging of the human body and its clinical models, and also provides the basis for further research into the problem of premature aging of the body and age-related diseases.