Lack of an association between matrix metalloproteinase polymorphisms and coronary heart disease in a Han Chinese population

Genet Mol Res. 2015 Oct 9;14(4):12254-61. doi: 10.4238/2015.October.9.14.

Abstract

Coronary heart disease (CHD) has become a leading cause of human deaths worldwide. Recent studied showed that polymorphisms of the matrix metalloproteinase (MMP) genes played important roles in extracellular matrix remodeling and contribute to the pathogenesis of vascular diseases. Here, we investigated whether these MMP gene polymorphisms were associated with CHD in Han Chinese. Our case-control study was involved with 1509 unrelated individuals, including 777 CHD cases and 732 controls. We selected a total of five polymorphisms whose genotypes were determined using Sequenom iPLEX technology. Our results showed there were no significant associations between the five MMP gene polymorphisms and CHD risk at either genotype or allele levels (P > 0.05). Further subgroup analyses by sex were also unable to reveal any significant association (P > 0.05). In conclusion, no significant associations were found between the five MMP gene polymorphisms and the risk of CHD in Han Chinese.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People / genetics
  • Case-Control Studies
  • Coronary Artery Disease / enzymology*
  • Coronary Artery Disease / genetics*
  • Genetic Predisposition to Disease / genetics
  • Genotype
  • Humans
  • Matrix Metalloproteinase 1 / genetics
  • Matrix Metalloproteinase 12 / genetics
  • Matrix Metalloproteinase 13 / genetics
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase 9 / genetics
  • Matrix Metalloproteinases / genetics*
  • Polymorphism, Single Nucleotide / genetics*

Substances

  • Matrix Metalloproteinase 13
  • Matrix Metalloproteinases
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9
  • Matrix Metalloproteinase 12
  • Matrix Metalloproteinase 1