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The association between genetic polymorphisms of matrix metalloproteinases and knee osteoarthritis: A systematic review and meta-analysis.
Jiang, Xu; Wang, Qianqian; Wang, Chao; Zhang, Yanzhuo; Wei, Zhenjie; Wu, Zhimin; Yu, Shunan; Wu, Chengai.
Afiliação
  • Jiang X; Department of Orthopaedics, Beijing Jishuitan Hospital, Capital Medical University, Beijing, China.
  • Wang Q; Department of Molecular Orthopaedics, Beijing Research Institute of Traumatology and Orthopaedics, Beijing, China.
  • Wang C; Department of Molecular Orthopaedics, Beijing Research Institute of Traumatology and Orthopaedics, Beijing, China.
  • Zhang Y; Department of Molecular Orthopaedics, Beijing Research Institute of Traumatology and Orthopaedics, Beijing, China.
  • Wei Z; Department of Molecular Orthopaedics, Beijing Research Institute of Traumatology and Orthopaedics, Beijing, China.
  • Wu Z; Department of Molecular Orthopaedics, Beijing Research Institute of Traumatology and Orthopaedics, Beijing, China.
  • Yu S; Department of Molecular Orthopaedics, Beijing Research Institute of Traumatology and Orthopaedics, Beijing, China.
  • Wu C; Department of Molecular Orthopaedics, Beijing Research Institute of Traumatology and Orthopaedics, Beijing, China.
Int J Rheum Dis ; 27(3): e15123, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38514927
ABSTRACT

AIM:

To investigate the linkage of matrix metalloproteinase (MMP) gene polymorphisms with the pathogenesis of knee osteoarthritis (OA).

METHODS:

This meta-analysis study systematically retrieved relevant studies from PubMed, Embase, the Cochrane Central, Wanfang Data, CNKI, and SinoMed up to November 2020. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to estimate the association between MMP gene polymorphisms and OA.

RESULTS:

A total of nine case-control studies comprising 1719 knee OA patients and 1904 controls were included in this meta-analysis. The results revealed that MMP-1-1607 (rs1799750) 1G/2G polymorphism was not significantly associated with knee OA risk in four genetic models (OR (95% CI) allele model 0.89 (0.57, 1.40), p = .615); dominant mode 0.82 (0.47, 1.44), p = .486; recessive model 0.88 (0.49, 1.57), p = .659; homozygote model 0.79 (0.34, 1.82), p = .576. The association was significant for dominant model of MMP-3 C/T 1.54 (1.10-2.15), p = .013, especially in Asian ethnicity (1.63 (1.11, 2.39), p = .013). Variants of MMP-13 C/T polymorphism were associated with increased risk of knee OA development based on dominant model 1.56 (1.19, 2.06), p = .001 and homozygote model 2.12 (1.44, 3.13), p < .001, and there were significant associations between MMP-13 C/T polymorphism and knee OA risk in Asian ethnicity under different genetic models (all p > .05).

CONCLUSIONS:

Present evidence suggested that the gene polymorphisms of MMP-1-1607 1G/2G may not be associated with the risk of OA. But, the dominant model of MMP-3 and MMP-13 polymorphisms in Asian ethnicity was significantly correlated with knee OA.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoartrite do Joelho Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoartrite do Joelho Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article