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Plasma osteoprotegerin levels in the general population: relation to indices of left ventricular structure and
Torbjørn Omland1, Mark H Drazner, Thor Ueland
1Akershus University Hospital, Lorenskog, Norway. torbjorn.omland@medisin.uio.no
Insights
Higher osteoprotegerin levels correlate with adverse cardiac remodeling and reduced function in men and women. This suggests osteoprotegerin may contribute to heart disease development.
Area of Science:
- Cardiovascular Medicine
- Endocrinology
- Immunology
Background:
- Osteoprotegerin (OPG), a TNF receptor superfamily member, influences bone, endocrine, and immune systems.
- Elevated OPG is observed in myocardial tissue and circulation during heart failure.
- The association between OPG and cardiac structure/function in the general population remains unclear.
Purpose of the Study:
- To investigate the relationship between plasma osteoprotegerin levels and cardiac magnetic resonance imaging (MRI) indices of left ventricular (LV) structure and function.
- To assess these associations in a large, diverse cohort from the Dallas Heart Study.
Main Methods:
- Cross-sectional analysis of 2715 subjects from the Dallas Heart Study.
- Measurement of plasma osteoprotegerin levels.
- Cardiac MRI assessment of LV structure (mass, wall thickness, concentricity) and function (ejection fraction, end-systolic volume).
- Linear regression analysis, adjusting for multiple potential confounders.
Main Results:
- Higher OPG levels were significantly associated with increased LV mass, wall thickness, and concentricity, and decreased ejection fraction in both genders.
- After comprehensive adjustments, OPG remained significantly linked to these LV indices in men.
- In women, higher OPG was independently associated with increased LV end-systolic volume and lower ejection fraction, but not LV hypertrophy.
Conclusions:
- Osteoprotegerin is associated with adverse left ventricular remodeling and systolic dysfunction in the general population.
- These findings support a potential pathophysiological role for OPG in the development of left ventricular hypertrophy and dysfunction.
- Gender-specific associations highlight potential differences in OPG's cardiac impact.
Abstract:
Osteoprotegerin, a member of the tumor necrosis factor receptor superfamily, has pleiotropic effects on bone metabolism, endocrine function, and the immune system. Myocardial expression and circulating levels of osteoprotegerin are increased in heart failure. The relationship between osteoprotegerin levels in the general population and indices of left ventricular structure and function is unknown. Plasma osteoprotegerin levels and cardiac MRI indices of left ventricular structure and function were available in 2715 subjects (median age: 44 years; 45% male) enrolled in the Dallas Heart Study. The associations between osteoprotegerin concentration and indices of left ventricular structure and function were assessed by linear regression analysis, adjusting for possible confounders. By gender-specific linear regression analysis, higher osteoprotegerin levels were significantly associated with higher left ventricular mass, left ventricular wall thickness, left ventricular concentricity index, and lower left ventricular ejection fraction (P<0.001 for all). After adjustment for age, race, fat-free mass, fat mass, hypertension, diabetes, coronary artery disease, estimated glomerular filtration rate, hypercholesterolemia, smoking status, hormone replacement therapy, coronary artery calcium score >10, and presence of aortic plaque, osteoprotegerin remained significantly associated with each of these left ventricular indices among male subjects (P<0.05 for each). Among female subjects, higher osteoprotegerin was independently associated with higher left ventricular end-systolic volume and lower ejection fraction (P<0.0001 for each) but not with indices of left ventricular hypertrophy. These findings are compatible with the theory that osteoprotegerin may play a pathophysiological role in the development of left ventricular hypertrophy and systolic dysfunction.
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