Usefulness of Released Cardiac Myosin Binding Protein-C as a Predictor of Cardiovascular Events
Carl W Tong1, Giuseppina F Dusio2, Suresh Govindan3
1Department of Medical Physiology, Texas A&M University Health Science Center College of Medicine, Temple, Texas; Baylor Scott & White Health-Central Texas, Internal Medicine/Cardiology Division, Temple, Texas.
Insights
Cardiac myosin binding protein-C (cMyBP-C) indicates cardiovascular stress. Elevated prestress cMyBP-C levels predict future cardiovascular events, showing its potential as a sensitive screening biomarker for severe heart disease.
Area of Science:
- Cardiology
- Biomarker Discovery
- Clinical Medicine
Background:
- Cardiac myosin binding protein-C (cMyBP-C) is a heart muscle protein.
- Elevated serum cMyBP-C is linked to myocardial infarction (MI), but its predictive value for future cardiovascular disease is unclear.
Purpose of the Study:
- To investigate if circulating cMyBP-C levels predict cardiovascular stress and disease.
- To evaluate cMyBP-C as a sensitive indicator of cardiovascular risk.
Main Methods:
- Prospective study of 158 participants (75 men, 83 women).
- Exercise stress echocardiography with pre- and post-stress blood sampling for cMyBP-C levels.
- 1 to 1.5-year follow-up for primary and critical cardiovascular events.
Main Results:
- Exercise stress increased serum cMyBP-C in all subjects.
- A 96% sensitive prestress cMyBP-C threshold showed a hazard ratio of 8.1 for primary events (p=0.041).
- Prestress cMyBP-C had an area under the curve of 0.91 and hazard ratio of 13.8 for critical events (p=0.000472).
Conclusions:
- Basal cMyBP-C levels reflect susceptibility to various cardiovascular diseases.
- cMyBP-C demonstrates high sensitivity and potential as a screening biomarker for severe cardiovascular diseases.
Abstract:
Cardiac myosin binding protein-C (cMyBP-C) is a heart muscle-specific thick filament protein. Elevated level of serum cMyBP-C is an indicator of early myocardial infarction (MI), but its value as a predictor of future cardiovascular disease is unknown. Based on the presence of significant amount of cMyBP-C in the serum of previous study subjects independent of MI, we hypothesized that circulating cMyBP-C is a sensitive indicator of ongoing cardiovascular stress and disease. To test this hypothesis, 75 men and 83 women of similar ages were recruited for a prospective study. They underwent exercise stress echocardiography to provide pre- and poststress blood samples for subsequent determination of serum cMyBP-C levels. The subjects were followed for 1 to 1.5 years. Exercise stress increased serum cMyBP-C in all subjects. Twenty-seven primary events (such as death, MI, revascularization, invasive cardiovascular procedure, or cardiovascular-related hospitalization) and 7 critical events (CE; such as death, MI, stroke, or pulmonary embolism) occurred. After adjusting for sex and cardiovascular risk factors with multivariate Cox regression, a 96% sensitive prestress cMyBP-C threshold carried a hazard ratio of 8.1 with p = 0.041 for primary events. Most subjects (6 of 7) who had CE showed normal ejection fraction on echocardiography. Prestress cMyBP-C demonstrated area under receiver operating curve of 0.91 and multivariate Cox regression hazard ratio of 13.8 (p = 0.000472) for CE. Thus, basal cMyBP-C levels reflected susceptibility for a variety of cardiovascular diseases. Together with its high sensitivity, cMyBP-C holds potential as a screening biomarker for the existence of severe cardiovascular diseases.
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