AI Article Synopsis

  • As individuals age, changes in their cells and skeletal systems negatively impact bone fracture healing, particularly in the elderly who are more prone to hip fractures.
  • Research indicates that older adults show changes in specific immune cells (monocytes) that are important for bone healing, including increased activation and migration markers while having a decrease in co-inhibitory molecules.
  • Understanding the unique characteristics of monocytes and their role in fracture healing could lead to advancements in diagnosing and treating age-related hip fractures, potentially improving outcomes for older patients.

Article Abstract

Individual aged with various change in cell and cellular microenvironments and the skeletal system undergoes physiological changes that affect the process of bone fracture healing. These changes are accompanied by alterations in regulating critical genes involved in this healing process. Unfortunately, the elderly are particularly susceptible to hip bone fractures, which pose a significant burden associated with higher morbidity and mortality rates. A notable change in older adults is the increased expression of activation, adhesion, and migration markers in circulating monocytes. However, there is a decrease in the expression of co-inhibitory molecules. Recently, research evidence has shown that the migration of specific monocyte subsets to the site of hip fracture plays a crucial role in bone resorption and remodeling, especially concerning age-related factors. In this review, we summarize the current knowledge about uniqueness characteristics of monocytes, and their potential regulation and moderation to enhance the healing process of hip fractures. This breakthrough could significantly contribute to the comprehension of aging process at a fundamental aging mechanism through this initiative would represent a crucial stride for diagnosing and treating age related hip fracture.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10837905PMC
http://dx.doi.org/10.1186/s12979-024-00413-8DOI Listing

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