Abstract

Aseptic loosening is a major cause of revision surgery of total hip arthroplasty (THA). Only few host factors affecting aseptic loosening have been identified until now, although they are urgently needed to identify and possibly treat those patients at higher risk for aseptic loosening. To determine whether the functional single nucleotide polymorphism (SNP) c.-938C>A (rs2279115), located in the promoter region of the BCL2 gene has an impact on aseptic loosening of THA we genotyped and analyzed 234 patients suffering from aseptic loosening and 231 patients after primary THA. The polymorphism is associated with risk for aseptic loosening with the CC genotype at highest risk for aseptic loosening, Odds Ratio CC vs. AA 1.93, 95%CI 1.15–3.25, p = 0.013. In contrast, low risk AA genotype carriers that still developed aseptic loosening showed a significantly shorter time to aseptic loosening than patients carrying the C allele (p = 0.004). These results indicate that the BCL2 -938C>A polymorphism influences the occurrence and course of aseptic loosening and suggests this polymorphism as an interesting candidate for prospective studies and analyses in THA registers.

Highlights

  • Aseptic loosening is a major cause for revision surgery after total hip arthroplasty (THA)

  • Our goal was to determine whether the BCL2 -938C>A polymorphism influences the course and occurrence of aseptic loosening of THA

  • Our results indicate that the BCL2 -938C>A polymorphism has a relevant impact on aseptic loosening of THA because genotypes were significantly associated with risk of aseptic loosening as well as time to aseptic loosening

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Summary

Introduction

Aseptic loosening is a major cause for revision surgery after total hip arthroplasty (THA). Studies suggest that it accounts for more than 55% of all failures in THA [1]. Few host factors affecting aseptic loosening have been identified until now [2, 3]. In recent years genetic variations in different genes were investigated for putative impact on aseptic loosening [4]. These candidate gene approach studies analyzed different signaling cascades, e.g. inflammatory cytokine genes, but not the apoptosis pathway.

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