Key result
The ACE DD genotype significantly increased the risk of premature coronary artery disease by 9% (RR 1.09) compared to II or ID genotypes.
Why the study?
Angiotensin-converting enzyme is related to cardiometabolic risk and atherosclerosis, but whether the ACE insertion/deletion variant impacts cardiometabolic risk factors, premature coronary artery disease, and coronary lesion severity required investigation.
Does the ACE DD genotype increase cardiometabolic risk factors, premature coronary artery disease, and severity of coronary lesions compared to II or ID genotypes?
Meta-Analysis (n=94,270)
Does the ACE DD genotype increase cardiometabolic risk factors, premature coronary artery disease, and severity of coronary lesions compared to II or ID genotypes?
Relative Risk: 1.09 (95% CI 1.03–1.15)
p-value: p=<0.01
The ACE DD genotype is associated with a slight but significant increase in cardiometabolic risk factors, premature coronary artery disease, and multiple vessel lesions, particularly in Caucasians and males.
Angiotensin-converting enzyme (ACE) is closely related to cardiometabolic risk factors and atherosclerosis. This study aims to investigate whether the insertion/deletion (I/D) variant of ACE gene impacts cardiometabolic risk factors, premature coronary artery disease (PCAD), and severity of coronary lesions. PubMed, Cochrane Library, Central, CINAHL, and ClinicalTrials.gov were searched until December 22, 2023. 94,270 individuals were included for the analysis. Carriers of DD genotype had higher levels of triglycerides (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), systolic blood pressure (SBP), diastolic blood pressure (DBP), body mass index (BMI), and waist circumference (WC) than carriers of II or ID genotypes. In addition, carriers of DD genotype were at high risk of PCAD and multiple vessel lesions. The impacts of ACE I/D variant on lipid levels were significant in American individuals but stronger in male individuals. In contrast, the impacts of ACE I/D variant on PCAD and severity of coronary lesions were primarily significant in Caucasian individuals. This study indicates that the ACE I/D variant has a slight but significant impact on cardiometabolic risk factors, PCAD, and severity of coronary lesions. Angiotensin-converting enzyme inhibitors (ACEI) may benefit high-risk populations with ACE DD genotype to prevent PCAD and multiple vessel lesions.PROSPERO registration number: CRD42023426732.
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Zhi Luo (2024) conducted a meta-analysis in Premature coronary artery disease, severity of coronary lesions, and cardiometabolic risk factors (n=94,270). ACE DD genotype vs. ACE II or ID genotypes was evaluated on Premature coronary artery disease (PCAD) risk (Recessive model: DD vs II+ID) (RR 1.09, 95% CI 1.03-1.15, p=<0.01). The ACE DD genotype significantly increased the risk of premature coronary artery disease by 9% (RR 1.09) compared to II or ID genotypes.
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