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Association between ACR1 gene product expression and cardiomyopathy in children
Yan Wang1, Ling Niu1, Xiuhua He1
1Department of Cardiology, Xuzhou Children's Hospital, Xuzhou, Jiangsu 221002, P.R. China.
Insights
Pediatric cardiomyopathy involves increased morbidity, but effective treatments remain elusive. This study found reduced ACR1 gene product levels in children with cardiomyopathy, suggesting a link between ACR1 inhibition and disease development.
Area of Science:
- Cardiology
- Genetics
- Molecular Biology
Background:
- Pediatric cardiomyopathy is a serious condition with increasing morbidity and limited effective treatments.
- Understanding the molecular mechanisms underlying pediatric cardiomyopathy is crucial for developing new therapeutic strategies.
Purpose of the Study:
- To investigate the expression of ACR1 gene products in children diagnosed with cardiomyopathy.
- To determine the association between ACR1 expression levels and the pathogenesis of pediatric cardiomyopathy.
Main Methods:
- Quantified ACR1 mRNA and protein levels using RT-qPCR, ELISA, and Western blot analysis in 73 pediatric cardiomyopathy patients and 76 healthy controls.
- Utilized immunohistochemistry to examine ACR1 expression in cardiac tissue samples.
- Collected samples between April 2013 and April 2015.
Main Results:
- No significant difference in ACR1 mRNA levels was observed between patients and controls via RT-qPCR.
- ELISA and Western blot analysis revealed significantly lower ACR1 protein levels in pediatric cardiomyopathy patients.
- Immunohistochemistry indicated a progressive decrease in ACR1 levels correlating with disease progression in patients.
Conclusions:
- Inhibition of ACR1 gene expression is associated with the development and progression of pediatric cardiomyopathy.
- Reduced ACR1 levels represent a potential biomarker and therapeutic target for pediatric cardiomyopathy.
- Further research into ACR1's role can elucidate cardiomyopathy pathogenesis and inform treatment development.
Abstract:
Cardiomyopathy is a heterogeneous heart disease. Although morbidity of pediatric cardiomyopathy has been on the increase, effective treatments have not been identified. The aim of the study was to examine the expression of ACR1 gene products in association with cardiomyopathy in children. In total, 73 patients and 76 healthy subjects were enrolled in the study, from April, 2013 to April, 2015. The relative expression of ACR1 mRNA and protein were quantified in all cases, using reverse transcription-quantitative polymerase chain reaction (RT-qPCR), ELISA and western blot analysis. Immunohistochemistry was used to stain cardiac tissue samples to reveal differences between the patients and the control group. The results showed that the level of ACR1 mRNA by RT-qPCR was not different between the two study groups. However, ELISA and western blot analysis showed a significant difference, with patients expressing lower levels of ACR1. Additionally, immunohistochemistry revealed the levels of ACR1 were reduced in patients as the time course of disease increased. Thus, there is an association between the inhibition of ACR1 expression and the development of the disease. These findings are useful in the elucidation of the pathogenesis of pediatric cardiomyopathy, a severe disease with few effective treatment options available.
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