Publications by authors named "M Dalinghaus"

Background: Plasma renin activity (PRA) has gained relevance as prognostic marker in adults with heart failure. The use of PRA as a clinically meaningful parameter in children and children with heart failure requires a thorough knowledge of the factors that influence PRA to correctly assess PRA levels. We aim to evaluate the influence of age, heart failure and angiotensin-converting enzyme inhibitor (ACEi) on PRA levels in children.

View Article and Find Full Text PDF

Employing animal models to study heart failure (HF) has become indispensable to discover and test novel therapies, but their translatability remains challenging. Although cytoskeletal alterations are linked to HF, the tubulin signature of common experimental models has been incompletely defined. Here, we assessed the tubulin signature in a large set of human cardiac samples and myocardium of animal models with cardiac remodeling caused by pressure overload, myocardial infarction or a gene defect.

View Article and Find Full Text PDF

Pediatric cardiomyopathy (CM) represents a group of rare, severe disorders that affect the myocardium. To date, the etiology and mechanisms underlying pediatric CM are incompletely understood, hampering accurate diagnosis and individualized therapy development. Here, we identified biallelic variants in the highly conserved flightless-I (FLII) gene in 3 families with idiopathic, early-onset dilated CM.

View Article and Find Full Text PDF

A 14-year-old girl with trisomy 13 presented with signs of respiratory failure. This was caused by the rupture of a sinus of Valsalva aneurysm into the right atrium. A Konar Multifunctional Occluder was used for closure.

View Article and Find Full Text PDF
Article Synopsis
  • The study investigated the current practices and outcomes of genetic evaluations in Dutch children with dilated cardiomyopathy, focusing on genotype-phenotype correlations for prognosis.
  • A total of 144 children were analyzed, with 74% undergoing genetic testing; findings showed that 36% had likely pathogenic or pathogenic variants, which were linked to poorer outcomes.
  • The results suggest that genetic testing is crucial for predicting prognosis in these children, and it should be included in their clinical evaluations regardless of the initial diagnosis.
View Article and Find Full Text PDF