Biology of Sport
eISSN: 2083-1862
ISSN: 0860-021X
Biology of Sport
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2/2017
vol. 34
 
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abstract:
Original paper

Are genes encoding proteoglycans really associated with the risk of anterior cruciate ligament rupture?

P Cięszczyk
1
,
K Willard
2
,
P Gronek
3
,
P Zmijewski
4
,
G Trybek
5
,
J Gronek
3
,
M Weber-Rajek
6
,
P Stastny
7, 8
,
M Petr
7
,
E Lulińska-Kuklik
9
,
K Ficek
10
,
E Kemeryte-Riaubiene
11
,
E Maculewicz
12
,
AV September
2

1.
Department of Physical Culture and Health Promotion, University of Szczecin, Szczecin, Poland
2.
MRC/UCT Research Unit for Exercise Science & Sports Medicine, University of Cape Town, Cape Town, South Africa
3.
Department of Gymnastics and Dance, Academy of Physical Education, Poznan, Poland
4.
Institute of Sport – National Research Institute, Warsaw, Poland
5.
Department of Oral Surgery, Pomeranian Medical University, Szczecin, Poland
6.
Department of Physioterapy, Collegium Medicum Nicolaus Copernicus University, Bydgoszcz, Poland
7.
Department of Sport Games, Charles University in Prague, Prague, Czech Republic
8.
Faculty of Physical Culture, Palacky University in Olomouc
9.
Department of Physical Culture, Academy of Physical Education and Sport in Gdańsk, Gdansk, Poland
10.
Academy of Sport Education in Katowice, Katowice, Poland
11.
Faculty of Sport and Health Education, Lithuanian University of Educational Sciences, Vilnius, Lithuania
12.
Department of Hygiene and Physiology, Military Institute of Hygiene and Epidemiology, Warsaw, Poland
Biol. Sport 2017;34:97-103
DOI: https://doi.org/10.5114/biolsport.2017.64582
Online publish date: 2017/01/04
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Proteoglycans are considered integral structural components of tendon and ligament and have been implicated in the resistance of compressive forces, collagen fibrillogenesis, matrix remodelling and cell signalling. Several sequence variants within genes encoding proteoglycans were recently implicated in modulating anterior cruciate ligament ruptures (ACLR). This study aimed to test the previously implicated variants in proteoglycan and vascular epithelial growth factor encoding genes with risk of ACLR in a population from Poland. A case control genetic association study was conducted using DNA samples from 143 healthy participants without a history of ACL injuries (99 male and 44 females) (CON group) and 229 surgically diagnosed ACLR participants (158 males and 71 females). All samples were genotyped for the ACAN: rs1516797, BGN: rs1042103, rs1126499, DCN: rs516115 and VEGFA: rs699947 variants. Main findings included the (i) ACAN rs1516797 G/T genotype which was underrepresented in the CON group (CON: 36%, n=52, ACLR: 49%, n=112, p=0.017, OR=1.68, 95% CI 1.09 to 2.57) when all participants were investigated and (ii) the BGN rs1042103 A allele was significantly under-represented in the male CON group compared to the male ACLR group (CON: 39%, n=78, ACLR: 49%, n=156, p=0.029, OR=1.5, 95% CI 1.05 to 2.15). Furthermore, BGN inferred haplotypes were highlighted with altered ACLR susceptibility. Although the study implicated the ACAN and BGN genes (combination of genotype, allele and haplotype) in modulating ACLR susceptibility, several differences were noted with previous published findings.
keywords:

Proteoglycans, Biglycan, Decorin, Aggrecan, Vascular Endothelial Growth Factor A, Anterior Cruciate Ligament, Genetic Association Study, Haplotypes

  
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