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Published on: September 28, 2015
Association between angiotensin II type 1 receptor polymorphism and sudden cardiac death in myocardial infarction
Peter Kruzliak1, Gabriela Kovacova, Olga Pechanova
1Institute of Normal and Pathological Physiology and Centre of Excellence for Regulatory Role of Nitric Oxide in Civilisation Diseases, Slovak Academy of Sciences, Sienkiewiczova 1, 813 71 Bratislava, Slovakia ; Department of Cardiovascular Diseases, International Clinical Research Center, St. Anne's Faculty Hospital and Masaryk University, Pekarska 53, 602 00 Brno, Czech Republic.
Objective:
The renin-angiotensin system is involved in the pathogenesis of coronary artery disease and myocardial infarction (MI). Angiotensin II (Ang II) has many adverse effects such as vasoconstriction and vascular remodeling, and these actions are mediated by the angiotensin II type 1 receptor (AT1R).
Patients And Methods:
A total of 1376 patients were recruited from January 2010 to April 2012. The study group consisted of 749 patients with ACS (317 females and 432 males) and of 627 healthy controls.
Results:
The ACS patients demonstrated a lower proportion of AA genotypes and AC genotypes but higher proportions of CC genotypes than the control population. The AT1R CC genotype conferred a 2.76-fold higher risk of MI compared with the genotype AC and AA. In addition, the CC genotype was also associated with a 4.08 times higher risk of left anterior descending artery infarction and a 3.07 times higher risk of anterior wall infarction. We also found that the CC genotype was independently associated with sudden cardiac death.
In Summary:
This study demonstrated that the AT1R CC genotype is an independent risk factor for ACS incidence, and this genotype is associated with a greater ACS severity and greater risk of sudden cardiac death.
Insights
The angiotensin II type 1 receptor (AT1R) CC genotype is linked to increased risk of acute coronary syndrome (ACS) and myocardial infarction (MI). This genotype is also associated with more severe ACS and higher risk of sudden cardiac death.
Area of Science:
- Cardiovascular Genetics
- Molecular Cardiology
- Renal Physiology
Background:
- The renin-angiotensin system plays a role in coronary artery disease (CAD) and myocardial infarction (MI) pathogenesis.
- Angiotensin II (Ang II) mediates adverse effects like vasoconstriction and vascular remodeling via the angiotensin II type 1 receptor (AT1R).
Purpose of the Study:
- To investigate the association between angiotensin II type 1 receptor (AT1R) gene polymorphisms and acute coronary syndrome (ACS).
- To determine if specific AT1R genotypes correlate with MI risk and severity.
Main Methods:
- A cohort of 1376 individuals was studied, including 749 patients with ACS and 627 healthy controls.
- Genotyping for the AT1R gene was performed.
- Clinical outcomes, including MI and sudden cardiac death, were assessed in relation to genotype.
Main Results:
- Patients with ACS showed a higher prevalence of the AT1R CC genotype compared to controls.
- The AT1R CC genotype was associated with a 2.76-fold increased risk of MI.
- The CC genotype correlated with a higher risk of left anterior descending artery infarction, anterior wall infarction, and sudden cardiac death.
Conclusions:
- The AT1R CC genotype is an independent risk factor for ACS incidence.
- This genotype is linked to increased ACS severity and a greater risk of sudden cardiac death.
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