Circulating S-Glutathionylated cMyBP-C as a Biomarker for Cardiac Diastolic Dysfunction
Xiaoxu Zhou1, Euy-Myoung Jeong2, Hong Liu1
1Division of Cardiology Department of Medicine The Lillehei Heart InstituteUniversity of Minnesota Minneapolis MN.
Elevated circulating S-glutathionylated Cardiac myosin binding protein-C (cMyBP-C) indicates diastolic dysfunction (DD). This finding suggests S-glutathionylated cMyBP-C may serve as a novel biomarker for detecting DD across species.
Area of Science:
- Cardiology
- Biochemistry
- Biomarker Discovery
Background:
- Cardiac myosin binding protein-C (cMyBP-C) is crucial for regulating heart muscle contraction and relaxation.
- Elevated S-glutathionylation of cMyBP-C in the heart muscle is linked to diastolic dysfunction (DD) in animal models.
Purpose of the Study:
- To investigate if circulating S-glutathionylated cMyBP-C can serve as a biomarker for diastolic dysfunction (DD).
Main Methods:
- Diastolic dysfunction (DD) was assessed using echocardiography in humans, African Green monkeys, and mice.
- Circulating levels of S-glutathionylated cMyBP-C were measured via immunoprecipitation in blood samples.
Main Results:
- Humans, monkeys, and mice with DD exhibited significantly elevated levels of circulating S-glutathionylated cMyBP-C compared to controls.
- A positive correlation was observed between circulating S-glutathionylated cMyBP-C and DD in human participants.
Conclusions:
- Circulating S-glutathionylated cMyBP-C is elevated in individuals with DD across multiple species.
- S-glutathionylated cMyBP-C shows potential as a novel biomarker for the presence of diastolic dysfunction.
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