MMP20

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Matrix metalloproteinase-20 precursor (EC 3.4.24.-) (MMP-20) (Enamel metalloproteinase) (Enamelysin)

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Identification of the effects of aging-related gene-matrix metalloproteinase on allograft outcomes in kidney transplantation.

Aging plays a profound role in the ability of the kidney to function. Aging which varies among individuals, has been associated with the matrix metalloproteinase (MMP) 7 and 20 genes. This study was conducted to analyze correlations between polymorphisms of MMP genes [rs880197 in MMP7 (A>T) and rs1711437 in MMP20 (G>A)] and transplant outcomes in 235 recipients. Transplant outcomes were evaluated according to the sum of the A alleles in the recipients and the donors. The group with a high number of A alleles (≥3) was compared with the group with a low number (<3). The group with a high number of MMP7 A alleles showed a lower risk of chronic tubulointerstitial lesion than the group with a low number (P = .009). The group with a high number of MMP20 A alleles had showed better long-term kidney function at 10 years after transplantation than the group with a low number (P = .026). Furthermore, the group with a high number of MMP20 A alleles showed a trend toward better graft survival compared with the group with a low number, especially among recipients followed for >1 year (P = .022). Polymorphisms of MMP7 and MMP20 genes may be surrogate markers to predict long-term outcomes after kidney transplantation.

MeSH Terms

  • Adult
  • Age Factors
  • Aging
  • Female
  • Gene Frequency
  • Genotype
  • Graft Survival
  • Humans
  • Kidney Transplantation
  • Male
  • Matrix Metalloproteinase 20
  • Matrix Metalloproteinase 7
  • Middle Aged
  • Phenotype
  • Polymorphism, Genetic
  • Risk Factors
  • Time Factors
  • Treatment Outcome
  • Young Adult