Association between the MMP-1-1607 1G2G Polymorphism and Osteoarthritis Risk: A Systematic Review and Meta-Analysis

Abstract EN

Background.

Osteoarthritis (OA) is a common disease characterized by articular cartilage degeneration and secondary hyperosteogenesis.

Genetic factors are associated with the occurrence of OA.

While several studies have shown that the matrix metalloproteinase-1- (MMP-1-) 1607 1G/2G (rs1799750) polymorphism may be related to the occurrence and development of OA, there is inconsistency in the literature.

To better estimate the relationship between the MMP-1 gene polymorphism and OA, a comprehensive meta-analysis of relevant literature was carried out.

Results.

In total, seven studies comprising 1245 OA patients and 1230 controls were included in this meta-analysis.

The combined results revealed no significant association between the MMP-1-1607 1G/2G polymorphism and risk of OA in the five genetic models.

However, after Bonferroni correction, the results of subgroup analysis revealed a significant correlation between the MMP-1-1607 1G/2G polymorphism and OA susceptibility in the temporomandibular joint (TMJ) OA subgroup (allelic: 2G vs.

1G: OR=1.575, 95%CI=1.259–1.972, P<0.01; recessive: 2G2G vs.

1G1G+1G2G: OR=2.411, 95%CI=1.658–3.504, P<0.01; and homozygote: 2G2G vs.

1G1G: OR=2.313, 95%CI=1.341, 3.991, P=0.003), the younger subgroup (aged less than 60 years; allelic: 2G vs.

1G: OR=1.635, 95%CI=1.354, 1.974, P<0.01; dominant: 2G1G+2G2G vs.

1G1G: OR=1.622, 95%CI=1.158, 2.271, P=0.005; recessive: 2G2G vs.

1G1G+1G2G: OR=2.209, 95%CI=1.718, 2.840, P<0.01; and homozygote: 2G2G vs.

1G1G: OR=2.578, 95%CI=1.798, 3.696, P<0.01), the larger subgroup (N>300), and the hospital-based case-control study (HCC) subgroup.

The sensitivity analysis suggested that the results of the meta-analysis were stable and reliable.

Begg’s funnel plot and Egger’s test indicated that there was no publication bias in this study.

Conclusion.

Our meta-analysis indicated that although the MMP-1-1607 1G/2G polymorphism was not significantly associated with OA susceptibility among the whole sample, it played a key role in the etiology and development of TMJ OA and OA in people aged less than 60 years.