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Interactions between Gene Variants within the COL1A1 and COL5A1 Genes and Musculoskeletal Injuries in Physically Active Caucasian

The COL1A1 and COL5A1 variants have been associated with the risk of musculoskeletal injuries. Therefore, the main aim of the study was to investigate the association between three polymorphisms within two genes (rs1800012 in COL1A1, as well as rs12722 and rs13946 in COL5A1) and the reported, yet ra...

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Autores principales: Leźnicka, Katarzyna, Żyżniewska-Banaszak, Ewelina, Gębska, Magdalena, Machoy-Mokrzyńska, Anna, Krajewska-Pędzik, Anna, Maciejewska-Skrendo, Agnieszka, Leońska-Duniec, Agata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8307722/
https://www.ncbi.nlm.nih.gov/pubmed/34356072
http://dx.doi.org/10.3390/genes12071056
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author Leźnicka, Katarzyna
Żyżniewska-Banaszak, Ewelina
Gębska, Magdalena
Machoy-Mokrzyńska, Anna
Krajewska-Pędzik, Anna
Maciejewska-Skrendo, Agnieszka
Leońska-Duniec, Agata
author_facet Leźnicka, Katarzyna
Żyżniewska-Banaszak, Ewelina
Gębska, Magdalena
Machoy-Mokrzyńska, Anna
Krajewska-Pędzik, Anna
Maciejewska-Skrendo, Agnieszka
Leońska-Duniec, Agata
author_sort Leźnicka, Katarzyna
collection PubMed
description The COL1A1 and COL5A1 variants have been associated with the risk of musculoskeletal injuries. Therefore, the main aim of the study was to investigate the association between three polymorphisms within two genes (rs1800012 in COL1A1, as well as rs12722 and rs13946 in COL5A1) and the reported, yet rarely described in the literature, injuries of the joint and muscle area in a physically active Caucasian population. Polish students (n = 114) were recruited and divided into the following two groups: students with (n = 53) and without (n = 61) injures. Genotyping was carried out using real-time PCR. The results obtained revealed a statistically significant association between rs1800012 COL1A1 and injury under an overdominant model. Specifically, when adjusted for age and sex, the GT heterozygotes had a 2.2 times higher chance of being injured compared with both homozygotes (TT and GG, 95% CI 0.59–5.07, p = 0.040). However, no significant interaction between the COL5A1 variants, either individually or in haplotype combination, and susceptibility to injury were found. In addition, the gene–gene interaction analysis did not reveal important relationships with the musculoskeletal injury status. It was demonstrated that rs1800012 COL1A1 may be positively associated with physical activity-related injuries in a Caucasian population. Harboring the specific GT genotype may be linked to a higher risk of being injured.
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spelling pubmed-83077222021-07-25 Interactions between Gene Variants within the COL1A1 and COL5A1 Genes and Musculoskeletal Injuries in Physically Active Caucasian Leźnicka, Katarzyna Żyżniewska-Banaszak, Ewelina Gębska, Magdalena Machoy-Mokrzyńska, Anna Krajewska-Pędzik, Anna Maciejewska-Skrendo, Agnieszka Leońska-Duniec, Agata Genes (Basel) Article The COL1A1 and COL5A1 variants have been associated with the risk of musculoskeletal injuries. Therefore, the main aim of the study was to investigate the association between three polymorphisms within two genes (rs1800012 in COL1A1, as well as rs12722 and rs13946 in COL5A1) and the reported, yet rarely described in the literature, injuries of the joint and muscle area in a physically active Caucasian population. Polish students (n = 114) were recruited and divided into the following two groups: students with (n = 53) and without (n = 61) injures. Genotyping was carried out using real-time PCR. The results obtained revealed a statistically significant association between rs1800012 COL1A1 and injury under an overdominant model. Specifically, when adjusted for age and sex, the GT heterozygotes had a 2.2 times higher chance of being injured compared with both homozygotes (TT and GG, 95% CI 0.59–5.07, p = 0.040). However, no significant interaction between the COL5A1 variants, either individually or in haplotype combination, and susceptibility to injury were found. In addition, the gene–gene interaction analysis did not reveal important relationships with the musculoskeletal injury status. It was demonstrated that rs1800012 COL1A1 may be positively associated with physical activity-related injuries in a Caucasian population. Harboring the specific GT genotype may be linked to a higher risk of being injured. MDPI 2021-07-09 /pmc/articles/PMC8307722/ /pubmed/34356072 http://dx.doi.org/10.3390/genes12071056 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Leźnicka, Katarzyna
Żyżniewska-Banaszak, Ewelina
Gębska, Magdalena
Machoy-Mokrzyńska, Anna
Krajewska-Pędzik, Anna
Maciejewska-Skrendo, Agnieszka
Leońska-Duniec, Agata
Interactions between Gene Variants within the COL1A1 and COL5A1 Genes and Musculoskeletal Injuries in Physically Active Caucasian
title Interactions between Gene Variants within the COL1A1 and COL5A1 Genes and Musculoskeletal Injuries in Physically Active Caucasian
title_full Interactions between Gene Variants within the COL1A1 and COL5A1 Genes and Musculoskeletal Injuries in Physically Active Caucasian
title_fullStr Interactions between Gene Variants within the COL1A1 and COL5A1 Genes and Musculoskeletal Injuries in Physically Active Caucasian
title_full_unstemmed Interactions between Gene Variants within the COL1A1 and COL5A1 Genes and Musculoskeletal Injuries in Physically Active Caucasian
title_short Interactions between Gene Variants within the COL1A1 and COL5A1 Genes and Musculoskeletal Injuries in Physically Active Caucasian
title_sort interactions between gene variants within the col1a1 and col5a1 genes and musculoskeletal injuries in physically active caucasian
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8307722/
https://www.ncbi.nlm.nih.gov/pubmed/34356072
http://dx.doi.org/10.3390/genes12071056
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