Cargando…
Role of matrix metalloproteases 1/3 gene polymorphisms in patients with rotator cuff tear
An association of Matrix Metalloproteinases-1/3 (MMP-1/3) rs1799750/rs3025058 polymorphism with increased risk of rotator cuff tear (RCT) has been reported in a Brazilian population. However, this significant association has not been confirmed in the Chinese population. Genotyping was conducted by p...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830375/ https://www.ncbi.nlm.nih.gov/pubmed/31652448 http://dx.doi.org/10.1042/BSR20191549 |
_version_ | 1783465769469739008 |
---|---|
author | Miao, Kaisong Jiang, Lifeng Zhou, Xindie Wu, Lidong Huang, Yong Xu, Nanwei Zhang, Junjie Li, Jin |
author_facet | Miao, Kaisong Jiang, Lifeng Zhou, Xindie Wu, Lidong Huang, Yong Xu, Nanwei Zhang, Junjie Li, Jin |
author_sort | Miao, Kaisong |
collection | PubMed |
description | An association of Matrix Metalloproteinases-1/3 (MMP-1/3) rs1799750/rs3025058 polymorphism with increased risk of rotator cuff tear (RCT) has been reported in a Brazilian population. However, this significant association has not been confirmed in the Chinese population. Genotyping was conducted by polymerase chain reaction (PCR)-restriction fragment length polymorphism and direct sequencing. Our results demonstrated that individuals with the TT genotype had a significantly higher risk of RCT compared with those with the CC genotype. The increased risk of RCT progression was associated with the 2G allele of the rs1799750 polymorphism. No significant association was observed for genotypic and allelic frequencies of the rs3025058 polymorphism. A significant association of the MMP-1 rs1799750 polymorphism was observed with smokers, drinkers and people aged ≥60 years and non-diabetic people. Additionally, the MMP-1 rs1799750 polymorphism was associated with pre-operative stiffness in RCT patients. In conclusion, a significant correlation was identified between the MMP-1 rs1799750 polymorphism and RCT. The MMP-1 rs1799750 polymorphism might be considered as a biomarker of genetically high-risk RCT, helping to clarify the mechanism of RCT. |
format | Online Article Text |
id | pubmed-6830375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68303752019-11-12 Role of matrix metalloproteases 1/3 gene polymorphisms in patients with rotator cuff tear Miao, Kaisong Jiang, Lifeng Zhou, Xindie Wu, Lidong Huang, Yong Xu, Nanwei Zhang, Junjie Li, Jin Biosci Rep Mutation An association of Matrix Metalloproteinases-1/3 (MMP-1/3) rs1799750/rs3025058 polymorphism with increased risk of rotator cuff tear (RCT) has been reported in a Brazilian population. However, this significant association has not been confirmed in the Chinese population. Genotyping was conducted by polymerase chain reaction (PCR)-restriction fragment length polymorphism and direct sequencing. Our results demonstrated that individuals with the TT genotype had a significantly higher risk of RCT compared with those with the CC genotype. The increased risk of RCT progression was associated with the 2G allele of the rs1799750 polymorphism. No significant association was observed for genotypic and allelic frequencies of the rs3025058 polymorphism. A significant association of the MMP-1 rs1799750 polymorphism was observed with smokers, drinkers and people aged ≥60 years and non-diabetic people. Additionally, the MMP-1 rs1799750 polymorphism was associated with pre-operative stiffness in RCT patients. In conclusion, a significant correlation was identified between the MMP-1 rs1799750 polymorphism and RCT. The MMP-1 rs1799750 polymorphism might be considered as a biomarker of genetically high-risk RCT, helping to clarify the mechanism of RCT. Portland Press Ltd. 2019-10-21 /pmc/articles/PMC6830375/ /pubmed/31652448 http://dx.doi.org/10.1042/BSR20191549 Text en © 2019 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY). |
spellingShingle | Mutation Miao, Kaisong Jiang, Lifeng Zhou, Xindie Wu, Lidong Huang, Yong Xu, Nanwei Zhang, Junjie Li, Jin Role of matrix metalloproteases 1/3 gene polymorphisms in patients with rotator cuff tear |
title | Role of matrix metalloproteases 1/3 gene polymorphisms in patients with rotator cuff tear |
title_full | Role of matrix metalloproteases 1/3 gene polymorphisms in patients with rotator cuff tear |
title_fullStr | Role of matrix metalloproteases 1/3 gene polymorphisms in patients with rotator cuff tear |
title_full_unstemmed | Role of matrix metalloproteases 1/3 gene polymorphisms in patients with rotator cuff tear |
title_short | Role of matrix metalloproteases 1/3 gene polymorphisms in patients with rotator cuff tear |
title_sort | role of matrix metalloproteases 1/3 gene polymorphisms in patients with rotator cuff tear |
topic | Mutation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830375/ https://www.ncbi.nlm.nih.gov/pubmed/31652448 http://dx.doi.org/10.1042/BSR20191549 |
work_keys_str_mv | AT miaokaisong roleofmatrixmetalloproteases13genepolymorphismsinpatientswithrotatorcufftear AT jianglifeng roleofmatrixmetalloproteases13genepolymorphismsinpatientswithrotatorcufftear AT zhouxindie roleofmatrixmetalloproteases13genepolymorphismsinpatientswithrotatorcufftear AT wulidong roleofmatrixmetalloproteases13genepolymorphismsinpatientswithrotatorcufftear AT huangyong roleofmatrixmetalloproteases13genepolymorphismsinpatientswithrotatorcufftear AT xunanwei roleofmatrixmetalloproteases13genepolymorphismsinpatientswithrotatorcufftear AT zhangjunjie roleofmatrixmetalloproteases13genepolymorphismsinpatientswithrotatorcufftear AT lijin roleofmatrixmetalloproteases13genepolymorphismsinpatientswithrotatorcufftear |