4.6 Article

The COL5A1 Gene Is Associated With Increased Risk of Anterior Cruciate Ligament Ruptures in Female Participants

Journal

AMERICAN JOURNAL OF SPORTS MEDICINE
Volume 37, Issue 11, Pages 2234-2240

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/0363546509338266

Keywords

anterior cruciate ligament (ACL); soft tissue; collagen; tear; polymorphism

Funding

  1. National Research Foundation (NRF) of South Africa [FA2005021700015, FA2007032700010]
  2. University of Cape Town
  3. South African Medical Research Council (MRC)

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Background: Anterior cruciate ligament ruptures, especially to young female athletes, are a cause of major concern in the sports medicine fraternity. The major structural constituents of ligaments are collagens, specifically types I and V. Recently, the gene that encodes for the alpha 1 chain of type I collagen (COL1A1) has been shown to be associated with an increased risk of cruciate ligament ruptures. The COL5A1 gene, which encodes for the alpha 1 chain of type V collagen, has been shown to be associated with Achilles tendon injuries. Purpose: The study was conducted to determine ( 1) if 2 sequence variants ( BstUI and DpnII restriction fragment length polymorphisms [RFLPs]) within the COL5A1 gene are associated with an increased risk of anterior cruciate ligament ruptures, and ( 2) if there were any gender-specific positive associations between the 2 COL5A1 sequence variants and risk of anterior cruciate ligament ruptures. Study Design: Case control study; Level of evidence, 3. Methods: A total of 129 white participants ( 38 women) with surgically diagnosed anterior cruciate ligament ruptures and 216 physically active control participants ( 84 women) without any history of ACL injury were included in this case-control genetic association study. All participants were genotyped for the COL5A1 BstUI and DpnII RFLPs. Results: There was a significant difference in the BstUI RFLP genotype frequency between the anterior cruciate ligament rupture and physically active control groups among the female participants, but not the male participants. The CC genotype in the female participants was significantly underrepresented in the anterior cruciate ligament rupture group compared with the controls (27.4% vs 5.6%; odds ratio = 6.6; 95% confidence interval, 1.5-29.7; P = .006). There were no differences in the DpnII RFLP genotype distributions between the anterior cruciate ligament rupture and physically active control groups. Conclusion: The CC genotype of the COL5A1 BstUI RFLP was underrepresented in female participants with anterior cruciate ligament ruptures.

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