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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.

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