Abstract

ObjectiveGenetic factor plays an important role in early failure of total hip arthroplasty (aseptic loosening) etiology, and TIMP-1 gene may be involved. The present study was conducted to reveal possible association between TIMP-1 polymorphisms with the risk of early failure of total hip arthroplasty (THA) (aseptic loosening).MethodsThe TIMP-1 single nucleotide polymorphisms (SNPs) rs4898, rs6609533, and rs2070584 were genotyped in 59 subjects who were diagnosed as aseptic loosening after total hip arthroplasty and in 100 controls.ResultsThe TIMP-1 SNP rs4898 T allele in the case group was found to be 1.32 fold (P = 0.0013, 95% CI = 1.16 to 1.58) than the control group. Similarly, the G allele of rs6609533 was found to be associated with increased risk of aseptic loosening (OR = 1.78, 95% CI = 1.52 to 2.17, P < 0.0001). For SNP rs2070584, no statistical association was found (A vs. G, OR = 1.14, 95% CI = 0.97 to 1.40, P = 0.2028).ConclusionThe results showed that the TIMP-1 SNPs rs4898 and rs6609533 were associated with the increased risk of early aseptic loosening susceptibility.

Highlights

  • There are numerous patients with end stage arthritis treated with cemented total hip arthroplasty (THA), and the number is rapidly increasing [1,2,3,4]

  • This study aims to determine whether the tissue inhibitors of metalloproteinases (TIMPs)-1 single nucleotide polymorphisms (SNPs) rs4898, rs6609533, and rs2070584 were associated with failure of THA in Chinese Han population

  • Association of TIMP-1 polymorphisms with susceptibility to failure of THA As expected, the distribution of the genotypes of SNPs of TIMP-1 gene conformed to the Hardy–Weinberg equilibrium and the genotyping success rate was 100%

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Summary

Results

Association of TIMP-1 polymorphisms with susceptibility to failure of THA As expected, the distribution of the genotypes of SNPs of TIMP-1 gene conformed to the Hardy–Weinberg equilibrium and the genotyping success rate was 100%. The TIMP-1 SNPs rs4898 and rs6609533 were found to be significantly associated with an increased risk of THA failure after adjustment of age, gender, and BMI. The TIMP-1 SNP rs4898 T allele in the case group was found to be 1.32 fold (P = 0.0013, 95% CI = 1.16 to 1.58) than the control group. The G allele of rs6609533 was found to be associated with an increased risk of aseptic loosening (OR = 1.78, 95% CI = 1.52 to 2.17, P < 0.0001). The LD within TIMP-1 gene was only found between rs4898 and rs6609533, showing that these two polymorphisms belong to one haploblock (Figure 1)

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21. Woessner JF Jr

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