Why the study?
Dilated cardiomyopathy is a leading cause of death in children with heart failure, but treatment outcomes are inconsistent and large cohort studies are lacking.
Population
6 children with DCM aged 0.5, 0.75, 5, 6, 12, and 13 years
Design
Single nuclei RNA sequencing study
Authors
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Offers cellular signatures for pediatric DCM; hypothesis-generating and requires validation before clinical translation.
Nicin et al. (2021) studied this question.
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