Key result
ACE I/D polymorphism linked to ~2.2-fold higher susceptibility to rheumatoid arthritis.
Why the study?
The association between ACE I/D polymorphism and susceptibility to psoriasis, vitiligo, and rheumatoid arthritis was unclear and required synthesis through meta-analysis.
Meta-Analysis (n=4,965)
Odds Ratio: 2.199 (95% CI 1.379–3.506)
p-value: p=0.001
Hypothesis-generating for ACE I/D in rheumatoid arthritis risk, especially Arabs; prospective validation required before any clinical use.
INTRODUCTION: The purpose of this study was to examine whether the insertion (I) and deletion (D) of angiotensin-converting enzyme (ACE) polymorphism confers susceptibility to psoriasis, vitiligo and rheumatoid arthritis (RA). MATERIALS AND METHODS: A meta-analysis was conducted on the association between the ACE I/D polymorphisms and psoriasis, vitiligo and RA. RESULTS: Fifteen studies comprising five on psoriasis, five on vitiligo and five on RA were available for the meta-analysis consisting of 2094 cases and 2871 controls. Meta-analysis of the DD+ID genotype showed significant associations with psoriasis (odds ratio (OR) 0.753, 95% confidence interval (CI) 0.601-0.921, p = 0.006). Meta-analysis showed no association between vitiligo and the ACE I/D polymorphism. Meta-analysis of the DD+ID genotype showed an association with RA (OR 2.199, 95% CI 1.379-3.506, p = 0.001). Ethnicity-specific meta-analysis of the D allele showed no association with psoriasis in Europeans, and vitiligo in South Asians. However, subgroup analysis by ethnicity revealed a significant association between the D allele and RA in Arab populations (OR 2.697, 95% CI 1.803-4.034, p = 1.3 × 10(-5)). CONCLUSIONS: Our meta-analysis demonstrates that the ACE I/D polymorphism is associated with susceptibility to RA, especially in Arab populations.
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Song et al. (2013) conducted a meta-analysis in Rheumatoid arthritis, psoriasis, and vitiligo (n=4,965). ACE I/D polymorphism (DD+ID genotype) vs. Reference genotype (controls) was evaluated on Susceptibility to rheumatoid arthritis (OR 2.199, 95% CI 1.379-3.506, p=0.001). The ACE I/D polymorphism (DD+ID genotype) was significantly associated with an increased susceptibility to rheumatoid arthritis (OR 2.199), particularly in Arab populations.
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