Association between the ACE insertion/deletion polymorphism and pterygium in Sardinian patients: a population based case-control study

BMJ Open. 2014 Oct 23;4(10):e005627. doi: 10.1136/bmjopen-2014-005627.

Abstract

Objective: The purpose of the study was to examine whether the insertion (I) and/or deletion (D) polymorphism of ACE confers susceptibility to primary pterygium in Sardinian patients in a case-control study.

Methods and results: Polymorphism genotyping was performed by nested PCR using genomic DNA extracted from the whole peripheral blood of participants with (n=251) and without (n=260) pterygium. DD, ID and II genotype frequencies were: 48%, 39% and 13%, respectively, for patients with pterygium, and 15%, 40% and 44%, respectively, for the control group. A statistically significant difference was found between the pterygium and control groups for the ACE I/D polymorphism (p<0.001). Moreover, a statistically significant difference was found between the DD and II groups (p<0.01; OR=10.49; 95% CI 6.18 to 17.79), DD+ID versus II group (p<0.01; OR=5.23; 95% CI 3.37 to 8.13) and DD versus ID groups (p<0.01; OR=3.21; 95% CI 2.04 to 5.04).

Conclusions: Statistical analysis showed that the DD genotype is associated with an increased risk of developing pterygium, and with a good chance that the D allele may play an important role in the development of disease.

Keywords: OPHTHALMOLOGY.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Case-Control Studies
  • Female
  • Gene Deletion
  • Humans
  • INDEL Mutation
  • Italy
  • Male
  • Middle Aged
  • Mutagenesis, Insertional
  • Peptidyl-Dipeptidase A / genetics*
  • Pterygium / genetics*
  • White People / genetics

Substances

  • ACE protein, human
  • Peptidyl-Dipeptidase A