Key result
The ACE insertion-deletion polymorphism was not significantly associated with primary open-angle glaucoma, showing similar genotype distributions (P=0.1) and allele frequencies (P=0.8) between groups.
Why the study?
Is the angiotensin-converting enzyme (ACE) insertion-deletion (I/D) polymorphism associated with primary open-angle glaucoma (POAG)?
Case-Control (n=205)
Is the angiotensin-converting enzyme (ACE) insertion-deletion (I/D) polymorphism associated with primary open-angle glaucoma (POAG)?
The ACE I/D polymorphism does not appear to be significantly associated with primary open-angle glaucoma in this cohort.
PURPOSE: To investigate the hypothesis that primary open-angle glaucoma (POAG) is associated with a common insertion-deletion (I/D) polymorphism in the angiotensin-converting enzyme (ACE) gene. METHODS: ACE I/D polymorphism was investigated in a control group of healthy subjects (n = 101) and in a group of patients diagnosed with POAG (n = 104). Polymerase chain reaction detection of I/D polymorphism was used to determine the presence of the two ACE alleles in the groups. RESULTS: Neither the I/D genotype distributions nor the allele frequencies differed significantly between POAG and control subjects (DD genotype 34.6 vs. 39.6%; ID genotype 53.9 vs. 40.6%; II genotype 11.5 vs. 19.8%, p = 0.1; D allele 61.5 vs. 60%; I allele 38.5 vs. 40%, p = 0.8). CONCLUSION: We could not identify a possible association of the I/D polymorphism in the ACE gene with POAG, however further studies with larger patient numbers in different populations are required to clarify the role of ACE gene in susceptibility to POAG.
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Özkur et al. (2004) conducted a case-control in Primary open-angle glaucoma (n=205). Angiotensin-converting enzyme (ACE) insertion-deletion (I/D) polymorphism vs. Healthy controls was evaluated on I/D genotype distributions and allele frequencies (p=0.1). The ACE insertion-deletion polymorphism was not significantly associated with primary open-angle glaucoma, showing similar genotype distributions (P=0.1) and allele frequencies (P=0.8) between groups.
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