2020
DOI: 10.1007/s00059-020-04903-5
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Dilated cardiomyopathies and non-compaction cardiomyopathy

Abstract: Dilated cardiomyopathy (DCM) is the most common form of cardiomyopathy and one of the most common causes of heart failure. It is characterized by left or biventricular dilation and a reduced systolic function. The causes are manifold and range from myocarditis to alcohol and other toxins, to rheumatological, endocrinological, and metabolic diseases. Peripartum cardiomyopathy is a special form that occurs at the end of or shortly after pregnancy. Genetic mutations can be detected in approximately 30-50% of DCM … Show more

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Cited by 27 publications
(20 citation statements)
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“…The pathway pathways involving overexpressed mRNA not only show cellular metabolic pathways such as citric acid cycle (TCA cycle) and oxidative phosphorylation but also are related to atherosclerosis, viral infection, and even a variety of neurodegenerative diseases (Parkinson's disease, Huntington's disease, Alzheimer's disease, etc.). The diversity of pathways in which it is involved corresponds to its various pathogenic factors such as cardiotoxic compounds, metabolism, rheumatological and endocrine diseases, and cellular infiltration and viral infection [16]. Due to multiple heterogeneous etiologies, dilated cardiomyopathy is an "umbrella" term that describes the final common pathway of different pathogenic processes and gene-environment interactions [17].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The pathway pathways involving overexpressed mRNA not only show cellular metabolic pathways such as citric acid cycle (TCA cycle) and oxidative phosphorylation but also are related to atherosclerosis, viral infection, and even a variety of neurodegenerative diseases (Parkinson's disease, Huntington's disease, Alzheimer's disease, etc.). The diversity of pathways in which it is involved corresponds to its various pathogenic factors such as cardiotoxic compounds, metabolism, rheumatological and endocrine diseases, and cellular infiltration and viral infection [16]. Due to multiple heterogeneous etiologies, dilated cardiomyopathy is an "umbrella" term that describes the final common pathway of different pathogenic processes and gene-environment interactions [17].…”
Section: Discussionmentioning
confidence: 99%
“…In most cases, dilated cardiomyopathy treatment refers to heart failure treatment based on medical treatment with angiotensin-converting enzyme inhibitors (angiotensin receptor blockers or angiotensin receptor/neprilysin inhibitors, if applicable), beta-blockers, and mineralocorticoid receptor antagonists according to current guidelines for heart failure [16]. Different from the previous ideas of symptomatic treatment with drugs to delay disease progression, this study selects the corresponding drugs through multiple Journal of Nanomaterials pharmacogenomics databases based on the new thinking of targeted therapy for specific disease mechanisms to reverse the disease process, targeting the 12 mRNAs overexpressed in the network and their encoded proteins, and the mechanistic analysis of the downregulation of mRNA expression and inhibition of proteins by these drugs in the future will further reveal the common pathways of their effects, which can be used as the starting point for subsequent studies.…”
Section: Discussionmentioning
confidence: 99%
“…Thus, BBR could improve EAM by differentially regulating the activities of p-STAT1, p-STAT3 and p-STAT4, which further inhibited the differentiation of Th17 and Th1 cells ( Liu et al, 2016 ). Dilated cardiomyopathy is the most common form of cardiomyopathy induced by a variety of causes, ranging from myocarditis to alcohol and other toxins such as drugs, cardiotoxins and chemotherapeutic agents, to rheumatic, endocrine and metabolic diseases, all of which can lead to reduced left ventricular systolic function and left ventricular or biventricular dilatation ( Hänselmann et al, 2020 ). The anthracycline anticancer drug doxorubicin (DOX) is an effective and commonly used chemotherapeutic agent for the treatment of malignancies, and its main side effect is cardiotoxicity.…”
Section: Myocarditis and Cardiomyopathymentioning
confidence: 99%
“…In 30–50% of cases of DCM in humans, a genetic cause can be found. 13 To date, more than 30 genes are known to cause DCM in humans. 14 Most affected genes code for ion channels, sarcomeres, Z-discs, nuclear proteins and desmosomes but 20% are found in the gene that encodes for titin.…”
Section: Dilated Cardiomyopathymentioning
confidence: 99%