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Osteoprotegerin inhibits vascular calcification without affecting atherosclerosis in ldlr(-/-) mice. | LitMetric

AI Article Synopsis

  • Recent studies show that higher levels of osteoprotegerin are linked to worse outcomes in vascular diseases like coronary artery disease and atherosclerosis, though its exact role remains uncertain.
  • In a study with mice on an atherogenic diet, those receiving osteoprotegerin treatment had reduced areas of calcified lesions, despite continuing atherosclerosis progression.
  • The findings suggest that osteoprotegerin may act primarily as an inhibitor of vascular calcification, rather than causing or worsening atherosclerosis.

Article Abstract

Background: The role of osteoprotegerin in vascular disease is unclear. Recent observational studies show that serum osteoprotegerin levels are associated with the severity and progression of coronary artery disease, atherosclerosis, and vascular calcification in patients. However, genetic and treatment studies in mice suggest that osteoprotegerin may protect against vascular calcification.

Methods And Results: To test whether osteoprotegerin induces or prevents vascular disease, we treated atherogenic diet-fed ldlr(-/-) mice with recombinant osteoprotegerin (Fc-OPG) or vehicle for 5 months. Vehicle-treated mice developed significant, progressive atherosclerosis with increased plasma osteoprotegerin levels, consistent with observational studies, and approximately 15% of these atherosclerotic lesions developed calcified cartilage-like metaplasia. Treatment with Fc-OPG significantly reduced the calcified lesion area without affecting atherosclerotic lesion size or number, vascular cytokines, or plasma cholesterol levels. Treatment also significantly reduced tissue levels of aortic osteocalcin, a marker of mineralization.

Conclusions: These data support a role for osteoprotegerin in the vasculature as an inhibitor of calcification and a marker, rather than a mediator, of atherosclerosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680735PMC
http://dx.doi.org/10.1161/CIRCULATIONAHA.107.707380DOI Listing

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