Journal of Science and Medicine in Sport
Volume 13, Issue 6 , Pages 630-632, November 2010

A functional variant within the MMP3 gene does not associate with human range of motion

  • Michael Posthumus

      Affiliations

    • The Division of Health and Life Sciences, University of Northampton, Northampton, United Kingdom
    • Corresponding Author InformationCorresponding author.
  • ,
  • Stuart M. Raleigh

      Affiliations

    • The Division of Health and Life Sciences, University of Northampton, Northampton, United Kingdom
  • ,
  • William J. Ribbans

      Affiliations

    • The Division of Health and Life Sciences, University of Northampton, Northampton, United Kingdom
  • ,
  • Martin P. Schwellnus

      Affiliations

    • UCT/MRC Research Unit for Exercise Science and Sports Medicine of the Department of Human Biology, Faculty of Health Sciences, University of Cape Town, South Africa
  • ,
  • Malcolm Collins

      Affiliations

    • UCT/MRC Research Unit for Exercise Science and Sports Medicine of the Department of Human Biology, Faculty of Health Sciences, University of Cape Town, South Africa
    • South African Medical Research Council, Cape Town, South Africa

Received 26 October 2009; received in revised form 18 January 2010; accepted 28 January 2010. published online 01 April 2010.

Abstract 

A recent heritability study has demonstrated that human range of motion (ROM) has a substantial genetic component. Furthermore, the COL5A1 BstUI RFLP has now been identified as the first gene variant to be associated with human ROM. Interestingly, this variant is known to interact with a functional variant within the MMP3 gene (rs679620) to increase risk of Achilles tendinopathy. We sought to determine whether the MMP3 rs679620 variant was associated with ROM both as a single marker and as an interacting marker with the COL5A1 BstUI RFLP. One hundred and twenty one participants were included in this study. All participants were genotyped for the MMP3 rs679620 variant, and performed passive straight leg raise (SLR) and sit and reach (SR) measurements. There were no significant differences in left leg SLR (L-SLR), right leg SLR (R-SLR), or SR measurements between the genotype groups (L-SLR, P=0.494; R-SLR, P=0.435; SR, P=0.266). Furthermore, there was no evidence of an interaction between the COL5A1 BstUI RFLP and the MMP3 rs679620 variant. Our study suggests that the MMP3 rs679620 variant does not associate with passive ROM.

Keywords: Stretching, Flexibility, Matrix metalloproteinase, Association, Polymorphism, Genotype

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PII: S1440-2440(10)00036-8

doi:10.1016/j.jsams.2010.01.006

Journal of Science and Medicine in Sport
Volume 13, Issue 6 , Pages 630-632, November 2010