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Published on: April 13, 2018
MMP3 -1171 5A/6A Promoter Genotype Influences Serum MMP3 Levels and Is Associated with Deep Venous Thrombosis
Xiang-Ping Li1, Guang-Zhen Wan2, Guang-Jian Wang3
1Department of Emergency Orthopedics, Linyi People's Hospital of Shandong Province, Linyi, Shandong, P.R. China.
Background:
The aim of this study was to investigate the roles of MMP3 (matrix metalloproteinase-3) gene polymorphism and protein expression in deep venous thrombosis (DVT) among Chinese Han population.
Methods:
A total of 280 subjects were included in this study and categorized as case group (144 DVT patients) and control group (136 healthy individuals). Polymerase chain reaction-restriction fragment length polymorphism was used to detect MMP3 promoter -1171 5A>6A genotype and allele frequencies. MMP3 serum levels were measured by enzyme-linked immunosorbent assay. SPSS version 18.0 statistical software was used for data analysis.
Results:
There was significant difference in genotype frequencies of MMP3 gene -1171 5A>6A between the case group and the control group (all P < 0.05). Furthermore, the 6A allele on MMP3 -1171 5A>6A may be associated with increased risk of DVT (odds ratio 1.961, 95% confidence interval 1.309-2.939, P < 0.01). The MMP3 serum level in DVT patients was markedly higher than the control group (case group: 28.45 ± 10.97 vs.
Control Group:
18.18 ± 9.03, P < 0.05). Serum MMP3 level in DVT patients carrying 5A/6A and 6A/6A genotypes was higher than the control group (P < 0.05). The bilateral calf circumference difference was significantly higher in DVT patients than the control group among all the genotypes at MMP3 gene -1171 5A>6A (all P < 0.05).
Conclusion:
MMP3 gene -1171 5A>6A polymorphism and upregulated protein expression may be associated with DVT risk in Chinese Han population.
Insights
Matrix metalloproteinase-3 (MMP3) gene polymorphism and increased protein expression are linked to a higher risk of deep venous thrombosis (DVT) in the Chinese Han population. The 6A allele of MMP3 -1171 5A>6A may increase DVT susceptibility.
Area of Science:
- Genetics
- Molecular Biology
- Vascular Medicine
Background:
- Deep venous thrombosis (DVT) is a significant vascular condition.
- The role of matrix metalloproteinase-3 (MMP3) in DVT pathogenesis requires further investigation.
- Genetic variations and protein expression levels of MMP3 may influence DVT risk.
Purpose of the Study:
- To examine the association between MMP3 gene polymorphism (-1171 5A>6A) and protein expression with DVT in the Chinese Han population.
- To determine if specific MMP3 genotypes or alleles correlate with an increased risk of developing DVT.
- To assess MMP3 serum levels in DVT patients compared to healthy controls.
Main Methods:
- Genotyping of the MMP3 -1171 5A>6A promoter polymorphism using polymerase chain reaction-restriction fragment length polymorphism.
- Quantification of MMP3 serum levels via enzyme-linked immunosorbent assay.
- Statistical analysis of genotype frequencies, allele frequencies, and serum protein levels in 280 subjects (144 DVT patients, 136 controls).
Main Results:
- Significant differences in MMP3 -1171 5A>6A genotype frequencies were observed between DVT patients and controls (P < 0.05).
- The 6A allele of MMP3 -1171 5A>6A was associated with an elevated risk of DVT (OR = 1.961, P < 0.01).
- MMP3 serum levels were significantly higher in DVT patients compared to controls (P < 0.05), particularly in those with 5A/6A and 6A/6A genotypes.
Conclusions:
- MMP3 gene -1171 5A>6A polymorphism is associated with DVT risk in the Chinese Han population.
- Upregulated MMP3 protein expression may play a role in the development of DVT.
- These findings suggest MMP3 as a potential genetic and molecular marker for DVT risk assessment.
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