Angiotensin converting enzyme DD genotype is associated with hypertensive crisis
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Published on: September 28, 2015
Gere Sunder-Plassmann1, Harald Kittler, Corinna Eberle
1Department of Medicine III, University of Vienna, Austria.
Insights
The angiotensin-converting enzyme (ACE) DD genotype may be linked to hypertensive crisis, particularly in men. This finding sheds light on the genetic factors contributing to this serious medical condition.
Area of Science:
- Genetics
- Cardiovascular Medicine
- Pharmacogenomics
Background:
- Hypertensive crisis is a serious medical condition with an unknown genetic basis.
- The renin-angiotensin-aldosterone system plays a crucial role in blood pressure regulation.
Purpose of the Study:
- To investigate the association between polymorphisms in renin-angiotensin-aldosterone system genes and hypertensive crisis.
- To identify potential genetic risk factors for hypertensive crisis.
Main Methods:
- A population-based case-control study was conducted.
- 182 patients with essential hypertension experiencing hypertensive crisis were compared to 182 healthy controls.
- Polymorphisms in genes including ACE, AGTR1, REN, RENBP, ADD1, and ADRB2 were analyzed using PCR and RFLP.
Main Results:
- The angiotensin-converting enzyme (ACE) I/D polymorphism deviated from Hardy-Weinberg equilibrium in patients.
- The DD genotype of the ACE gene was significantly more frequent in patients (38.5%) compared to controls (28.0%).
- This association was particularly strong in men, with the DD genotype found in 44% of male patients versus 25.3% of male controls.
Conclusions:
- A potential association exists between the DD genotype of the ACE gene and hypertensive crisis.
- The findings suggest that specific genetic variations may increase susceptibility to hypertensive crisis, especially in males.
Objective:
The genetic background of hypertensive crisis is unknown. We examined the association of polymorphisms in genes involved in the renin-angiotensin-aldosterone-system with hypertensive crisis.
Design:
Population-based case-control study.
Setting:
Emergency department at a tertiary care university hospital.
Patients:
A total of 182 patients with essential hypertension who were admitted to an emergency department for treatment of hypertensive crisis and 182 age- and sex-matched healthy individuals.
Interventions:
None.
Measurements:
Analysis of polymorphisms in genes coding for angiotensinogen (AJT 704T-->C), angiotensin II receptor 1 (AGTR1 1166A-->C), renin (REN 2646G-->A), renin-binding protein (RENBP 61T-->C), alpha-adducin (ADD1 1378G-->T), beta-2-adrenergic receptor (ADRB2 46A-->G, 79C-->G), and angiotensin I converting enzyme (ACE I/D) was performed by polymerase chain reaction and restriction fragment length polymorphism analysis. MAIN RESULTS Among patients, the ACE I/D polymorphism showed a deviation from Hardy-Weinberg equilibrium (p =.01). In controls, all polymorphisms were in the Hardy-Weinberg equilibrium. The frequency of the DD genotype was increased in patients (n = 70, 38.5%) vs. controls (n = 51; 28.0%;p =.03; odds ratio, 1.61; 95% confidence interval, 1.03-2.50), which was due to the DD genotype in 40 male patients (44%) vs. 23 in male controls (25.3%;p =.004; odds ratio, 3.48; 95% confidence interval, 1.47-8.30). There were no differences in genotype distributions among other polymorphisms.
Conclusion:
We demonstrate a possible association of the DD genotype with hypertensive crisis in men.
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