Key result
The ACE I/D polymorphism was not significantly associated with the risk of atherosclerosis in the overall population (adjusted OR 1.67 for DD vs II genotype).
Why the study?
The study sought to examine the relationship between the ACE I/D polymorphism (rs4646994) and atherosclerosis risk, as well as its potential effects on ACE activity and oxLDL levels.
Does ACE I/D polymorphism associate with atherosclerosis risk, ACE activity, and oxLDL levels in Western Iranians?
Case-Control (n=299)
No
Does ACE I/D polymorphism associate with atherosclerosis risk, ACE activity, and oxLDL levels in Western Iranians?
Odds Ratio: 1.67 (95% CI 0.73–3.83)
p-value: p=0.222
The ACE I/D polymorphism is not an independent risk factor for atherosclerosis in the overall Western Iranian population, though ACE activity and oxLDL levels are significantly elevated in patients with atherosclerosis.
No association found in this case-control study; leaves open any causal role of ACE I/D polymorphism in atherosclerosis.
BACKGROUND: It has been indicated that Angiotensin-Converting Enzyme Insertion/Deletion (ACE I/D) polymorphism (rs4646994) could be regarded as a genetic factor that raises the risk of CAD through its impact on the activity of Angiotensin-Converting Enzyme (ACE) and angiotensin II level. The present study seeks to examine the relationship between ACE I/D polymorphism with the risk of atherosclerosis. Moreover, its potential effects on ACE activity and oxLDL level are investigated. METHODS: In this study, 145 healthy individuals and 154 patients (143 males and 156 females) were selected among the subjects referred to Shahid Madani Hospital. Atherosclerosis was determined in all subjects with gold standard angiography. Blood samples were collected, used to isolate white blood cells (WBC) and serum separation. The DNA was extracted and the polymorphism was determined by polymerase chain reaction (PCR). The enzyme activity was measured using high-performance liquid chromatography (HPLC). RESULTS: This study indicated that patients with atherosclerosis had higher levels of oxidized Low-Density Lipoprotein (oxLDL) and ACE activity (P < 0.05) as compared to controls. Although we found a significant association between ACE I/D polymorphism genotype and the allele with atherosclerosis in the male group, there were no association when the entire patient group was compared to the entire control group. CONCLUSION: Our study revealed the ACE I/D polymorphism of the ACE gene may not be an independent risk factor in the development of atherosclerosis and evaluation of ACE activity level is more important in evaluating the risk of disease. The researchers found no relation between ACE I/D polymorphism and atherosclerosis and also between types of genotype, ACE activity, and OxLDL level.
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Nouryazdan et al. (2019) conducted a case-control in Atherosclerosis (n=299). ACE I/D polymorphism (DD genotype) vs. II genotype was evaluated on Risk of atherosclerosis (OR 1.67, 95% CI 0.73-3.83, p=0.222). The ACE I/D polymorphism was not significantly associated with the risk of atherosclerosis in the overall population (adjusted OR 1.67 for DD vs II genotype).
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