Genetics in orthopaedic practice

R. Aicale, D. Tarantino, G. Maccauro, G.M. Peretti, N. Maffulli

Article ID: 6730
Vol 33, Issue 2S1, 2019
DOI: https://doi.org/10.54517/jbrha6730
Received: 9 May 2019; Accepted: 9 May 2019; Available online: 9 May 2019; Issue release: 9 May 2019

Abstract

DNA holds genetic information in the nucleus of eukaryotic cells; and has three different functions: replication, storage of hereditary information, and regulation of cell division. Most studies described the association of single nucleotide polymorphism (SNP) to common orthopaedics diseases and the susceptibility to develop musculoskeletal injuries. Several mutations are associated with osteoporosis, musculoskeletal ailments and other musculoskeletal deformity and conditions. Several strategies, including gene therapy and tissue engineering with mesenchymal stem cells (MSC), have been proposed to enhance healing of musculoskeletal tissues. Furthermore, a recent technique has revolutionized gene editing: clustered regulatory interspaced short palindromic repeat (CRISPR) technology is characterized by simplicity in target design, affordability, versatility, and high efficiency, but needs more studies to become the preferred platform for genome editing. Predictive genomics DNA profiling allows to understand which genetic advantage, if any, may be exploited, and why a given rehabilitation protocol can be more effective in some individual than others. In conclusion, a better understanding of the genetic influence on the function of the musculoskeletal system and healing of its ailments is needed to plan and develop patient specific management strategies.


Keywords

crisp;DNA;genetics;muscles;rehabilitation;tendon


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