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Genetic Factors in Tendon Injury: A Systematic Review of the Literature
BACKGROUND: Tendon injury such as tendinopathy or rupture is common and has multiple etiologies, including both intrinsic and extrinsic factors. The genetic influence on susceptibility to tendon injury is not well understood. PURPOSE: To analyze the published literature regarding genetic factors ass...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571768/ https://www.ncbi.nlm.nih.gov/pubmed/28856171 http://dx.doi.org/10.1177/2325967117724416 |
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author | Vaughn, Natalie H. Stepanyan, Hayk Gallo, Robert A. Dhawan, Aman |
author_facet | Vaughn, Natalie H. Stepanyan, Hayk Gallo, Robert A. Dhawan, Aman |
author_sort | Vaughn, Natalie H. |
collection | PubMed |
description | BACKGROUND: Tendon injury such as tendinopathy or rupture is common and has multiple etiologies, including both intrinsic and extrinsic factors. The genetic influence on susceptibility to tendon injury is not well understood. PURPOSE: To analyze the published literature regarding genetic factors associated with tendon injury. STUDY DESIGN: Systematic review; Level of evidence, 3. METHODS: A systematic review of published literature was performed in concordance with the Preferred Reporting Items of Systematic Reviews and Meta-analysis (PRISMA) guidelines to identify current evidence for genetic predisposition to tendon injury. PubMed, Ovid, and ScienceDirect databases were searched. Studies were included for review if they specifically addressed genetic factors and tendon injuries in humans. Reviews, animal studies, or studies evaluating the influence of posttranscription factors and modifications (eg, proteins) were excluded. RESULTS: Overall, 460 studies were available for initial review. After application of inclusion and exclusion criteria, 11 articles were ultimately included for qualitative synthesis. Upon screening of references of these 11 articles, an additional 15 studies were included in the final review, for a total of 26 studies. The genetic factors with the strongest evidence of association with tendon injury were those involving type V collagen A1, tenascin-C, matrix metalloproteinase–3, and estrogen-related receptor beta. CONCLUSION: The published literature is limited to relatively homogenous populations, with only level 3 and level 4 data. Additional research is needed to make further conclusions about the genetic factors involved in tendon injury. |
format | Online Article Text |
id | pubmed-5571768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-55717682017-08-30 Genetic Factors in Tendon Injury: A Systematic Review of the Literature Vaughn, Natalie H. Stepanyan, Hayk Gallo, Robert A. Dhawan, Aman Orthop J Sports Med 40 BACKGROUND: Tendon injury such as tendinopathy or rupture is common and has multiple etiologies, including both intrinsic and extrinsic factors. The genetic influence on susceptibility to tendon injury is not well understood. PURPOSE: To analyze the published literature regarding genetic factors associated with tendon injury. STUDY DESIGN: Systematic review; Level of evidence, 3. METHODS: A systematic review of published literature was performed in concordance with the Preferred Reporting Items of Systematic Reviews and Meta-analysis (PRISMA) guidelines to identify current evidence for genetic predisposition to tendon injury. PubMed, Ovid, and ScienceDirect databases were searched. Studies were included for review if they specifically addressed genetic factors and tendon injuries in humans. Reviews, animal studies, or studies evaluating the influence of posttranscription factors and modifications (eg, proteins) were excluded. RESULTS: Overall, 460 studies were available for initial review. After application of inclusion and exclusion criteria, 11 articles were ultimately included for qualitative synthesis. Upon screening of references of these 11 articles, an additional 15 studies were included in the final review, for a total of 26 studies. The genetic factors with the strongest evidence of association with tendon injury were those involving type V collagen A1, tenascin-C, matrix metalloproteinase–3, and estrogen-related receptor beta. CONCLUSION: The published literature is limited to relatively homogenous populations, with only level 3 and level 4 data. Additional research is needed to make further conclusions about the genetic factors involved in tendon injury. SAGE Publications 2017-08-23 /pmc/articles/PMC5571768/ /pubmed/28856171 http://dx.doi.org/10.1177/2325967117724416 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc-nd/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License (http://www.creativecommons.org/licenses/by-nc-nd/3.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | 40 Vaughn, Natalie H. Stepanyan, Hayk Gallo, Robert A. Dhawan, Aman Genetic Factors in Tendon Injury: A Systematic Review of the Literature |
title | Genetic Factors in Tendon Injury: A Systematic Review of the Literature |
title_full | Genetic Factors in Tendon Injury: A Systematic Review of the Literature |
title_fullStr | Genetic Factors in Tendon Injury: A Systematic Review of the Literature |
title_full_unstemmed | Genetic Factors in Tendon Injury: A Systematic Review of the Literature |
title_short | Genetic Factors in Tendon Injury: A Systematic Review of the Literature |
title_sort | genetic factors in tendon injury: a systematic review of the literature |
topic | 40 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571768/ https://www.ncbi.nlm.nih.gov/pubmed/28856171 http://dx.doi.org/10.1177/2325967117724416 |
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