| Registro completo |
| Provedor de dados: |
BJMBR
|
| País: |
Brazil
|
| Título: |
Genetic variation of aggrecanase-2 (ADAMTS5) in susceptibility to osteoarthritis
|
| Autores: |
Zhou,Xindie
Jiang,Lifeng
Zhang,Yi
Zhang,Junjie
Zhou,Dong
Wu,Lidong
Huang,Yong
Xu,Nanwei
|
| Data: |
2019-01-01
|
| Ano: |
2019
|
| Palavras-chave: |
ADAMTS5
Polymorphism
Osteoarthritis
Co-expression analysis
|
| Resumo: |
Aggrecanase-2 (ADAMTS5) gene is responsible for aggrecan degradation that may contribute to cartilage destruction in a mouse osteoarthritis (OA) model. We aimed to investigate the effects of ADAMTS5 gene polymorphisms on OA risk in a Chinese population. A total of 300 OA patients and 300 controls were recruited and their genotypes for ADAMTS5 gene rs226794 and rs2830585 polymorphisms were determined using a custom-by-design 48-Plex single nucleotide polymorphism Scan™ kit. ADAMTS5-associated genes were identified by co-expression analysis and their functions were investigated by Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses. Bioinformatics analysis showed that ADAMTS5 was significantly related to the components, structural constituent, and organization of the extracellular matrix. The rs2830585 polymorphism, but not rs226794 polymorphism, was significantly associated with an increased risk of knee OA. Stratified analysis further confirmed this significant association in patients at age ≥55 years. In conclusion, the ADAMTS5 rs2830585 polymorphism may be involved in the development of knee OA by destroying the extracellular matrix, but this finding should be further confirmed by larger studies.
|
| Tipo: |
Info:eu-repo/semantics/article
|
| Idioma: |
Inglês
|
| Identificador: |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2019000200602
|
| Editor: |
Associação Brasileira de Divulgação Científica
|
| Relação: |
10.1590/1414-431x20188109
|
| Formato: |
text/html
|
| Fonte: |
Brazilian Journal of Medical and Biological Research v.52 n.2 2019
|
| Direitos: |
info:eu-repo/semantics/openAccess
|
