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. 2016 Apr 1;12(2):279-87.
doi: 10.5114/aoms.2015.50757. Epub 2016 Apr 12.

Impact of I/D polymorphism of ACE gene on risk of development and course of chronic obstructive pulmonary disease

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Impact of I/D polymorphism of ACE gene on risk of development and course of chronic obstructive pulmonary disease

Radosław Mlak et al. Arch Med Sci. .

Abstract

Introduction: Chronic obstructive pulmonary disease (COPD) affects more than 10% of the world's population over 40 years of age. The main exogenous risk factor is cigarette smoking; however, only 20% of smokers develop COPD, indicating that some other factors, e.g. genetic, may play an important role in the disease pathogenesis. Recent research indicates that ACE (angiotensin-converting enzyme) may be a susceptibility gene for asthma or COPD. The aim of our study was to determine the influence of I/D (insertion/deletion) polymorphism of the ACE gene (AluYa5, rs4646994) on the risk and course of COPD.

Material and methods: We investigated ACE I/D polymorphism in 206 COPD and 165 healthy Caucasian subjects.

Results: In the generalized linear model (GLZ) analysis of the influence of selected factors on presence of COPD we found a significant independent effect for male sex (repeatedly increases the risk of COPD, OR = 7.7, p = 0.049), as well as smoking or lower body mass index, but only in combination with older age (OR = 0.96, p = 0.003 and OR = 1.005, p = 0.04 respectively). Interestingly, analysis of factors which may influence the risk of a higher number of exacerbations demonstrated that occurrence of DD genotype, but only in men, is associated with a lower risk (OR = 0.7, p = 0.03) of this complication.

Conclusions: We suggest that ACE may not be a susceptibility gene for the origin of COPD but a disease-modifying gene. Since the impact of I/D polymorphism of the ACE gene on COPD risk is moderate or negligible, other molecular changes, that will help predict the development of this disease, should still be sought.

Keywords: ACE polymorphism; chronic obstructive pulmonary disease; exacerbation; renin-angiotensin-aldosterone system.

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Figures

Figure 1
Figure 1
Flow chart of recruitment and assessment
Figure 2
Figure 2
Representative electropherogram and analysis of ACE I/D polymorphism DD – deletion/deletion genotype, ID – insertion/deletion genotype, II – insertion/insertion genotype, bp – base pair.

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