
This review summarizes research on the physiological changes that occur with aging and the resulting effects on fracture healing.Aging affects the inflammatory response during fracture healing through senescence of the immune response and increased systemic pro-inflammatory status. Important cells of the inflammatory response, macrophages, T cells, mesenchymal stem cells, have demonstrated intrinsic age-related changes that could impact fracture healing. Additionally, vascularization and angiogenesis are impaired in fracture healing of the elderly. Finally, osteochondral cells and their progenitors demonstrate decreased activity and quantity within the callus. Age-related changes affect many of the biologic processes involved in fracture healing. However, the contributions of such changes do not fully explain the poorer healing outcomes and increased morbidity reported in elderly patients. Future research should address this gap in understanding in order to provide improved and more directed treatment options for the elderly population.
Aging, Physical Injury - Accidents and Adverse Effects, Immunosenescence, T-Lymphocytes, Clinical Sciences, 610, Neovascularization, Physiologic, Fracture healing, Clinical sciences, Regenerative Medicine, Senescence, Endocrinology & Metabolism, Elderly, Chondrocytes, Osteogenesis, 2.1 Biological and endogenous factors, Humans, Bony Callus, Physiologic, Neovascularization, Fracture Healing, Inflammation, Osteoblasts, Biomedical and Clinical Sciences, Macrophages, Stem Cells, Inflammatory response, Mesenchymal Stem Cells, Stem Cell Research, Inflamm-aging, Public Health and Health Services, Stem Cell Research - Nonembryonic - Non-Human, Chondrogenesis
Aging, Physical Injury - Accidents and Adverse Effects, Immunosenescence, T-Lymphocytes, Clinical Sciences, 610, Neovascularization, Physiologic, Fracture healing, Clinical sciences, Regenerative Medicine, Senescence, Endocrinology & Metabolism, Elderly, Chondrocytes, Osteogenesis, 2.1 Biological and endogenous factors, Humans, Bony Callus, Physiologic, Neovascularization, Fracture Healing, Inflammation, Osteoblasts, Biomedical and Clinical Sciences, Macrophages, Stem Cells, Inflammatory response, Mesenchymal Stem Cells, Stem Cell Research, Inflamm-aging, Public Health and Health Services, Stem Cell Research - Nonembryonic - Non-Human, Chondrogenesis
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