Objective: To review the current knowledge on bone health in patients with hemophilia A and the underlying pathogenetic mechanisms. Data Sources: Original research articles, meta-analyses, and scientific reviews. Data Synthesis: Already in childhood, patients with hemophilia A are prone to low bone mineral density, leading to osteopenia and/or osteoporosis. Initially associated with the life style of hemophilia, today we are faced with accumulating evidence that coagulation factor VIII is involved directly or indirectly in bone physiology. Conclusion: Understanding the role of factor VIII and the mechanisms of decreased bone mineral density in hemophilia A is critically important, especially as non-factor replacement therapies are available, and treatment decisions potentially impact bone health.
CITATION STYLE
Gebetsberger, J., Schirmer, M., Wurzer, W. J., & Streif, W. (2022, February 2). Low Bone Mineral Density in Hemophiliacs. Frontiers in Medicine. Frontiers Media S.A. https://doi.org/10.3389/fmed.2022.794456
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