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Possible association of ACE gene I/D polymorphism with blood pressure--lowering response to hydrochlorothiazide
Yong Zhou1, Shou-Ling Wu, Jian-Qing Liu
1Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China. yongzhou78214@163.com
Insights
The angiotensin-converting enzyme (ACE) I/D gene polymorphism influences hydrochlorothiazide (HCTZ) effectiveness. Patients with the DD genotype show a greater blood pressure reduction with HCTZ treatment.
Area of Science:
- Pharmacogenomics
- Cardiovascular Medicine
- Genetics
Background:
- Hydrochlorothiazide (HCTZ) is a widely used diuretic for hypertension management.
- Individual variability in drug response necessitates personalized treatment approaches.
- The angiotensin-converting enzyme (ACE) I/D gene polymorphism is a potential factor influencing cardiovascular drug efficacy.
Purpose of the Study:
- To investigate the association between ACE I/D gene polymorphism and the blood pressure-lowering response to HCTZ.
- To determine if specific ACE genotypes predict treatment outcomes in hypertensive patients receiving HCTZ.
Main Methods:
- A cohort of 829 patients was analyzed.
- Patients received a daily dose of 12.5 mg HCTZ for six weeks.
- Blood pressure reduction and achievement of target blood pressure were compared across different ACE genotype groups (II, ID, DD).
Main Results:
- Patients with the DD genotype exhibited significantly greater reductions in systolic blood pressure (SBP) and mean arterial pressure (MAP) compared to II or ID genotypes.
- The proportion of patients reaching target blood pressure was significantly higher in the DD genotype group.
- Pre-treatment SBP, MAP, aldosterone levels, and the DD genotype were identified as significant predictors in multi-linear regression models for SBP and MAP reduction.
Conclusions:
- ACE genotyping is significantly associated with the blood pressure-lowering response to HCTZ.
- Specific ACE genotypes may predict the efficacy of HCTZ as an antihypertensive treatment, supporting a personalized medicine approach.
Objective:
To explore the association between polymorphism in the ACE I/D gene and blood pressure-lowering response to hydrochlorothiazide (HCTZ) in 829 patients.
Methods:
HCTZ 12.5 mg was taken once a day for six weeks. The blood pressure reduction and ratio reaching target blood pressure were compared in different ACE genotype groups.
Results:
The reduction in SBP of patients carrying DD was greater than that in other groups carrying II or ID (12.2 mmHg versus 5.4 mmHg, 12.2 mmHg versus 4.4 mmHg, respectively, P<0.05). The reduction in MAP of patients carrying DD was also greater than that in other groups carrying II or ID (6.9 mmHg versus 3.9 mmHg, 6.9 mmHg versus 3.6 mmHg, respectively, P<0.05). The ratio reaching target blood pressure in DD groups was significantly higher than that in II or ID groups (P<0.05). The pre-treatment SBP, DD genotype, aldosterone levels entered the multi-linear regression model significantly and might affect the reduction of SBP. The pre-treatment DBP, aldosterone levels, DD genotype entered the multi-linear regression model significantly and might affect the reduction of DBP. The pre-treatment MAP, DD genotype, aldosterone levels entered the multi-linear regression model significantly and might affect the reduction of MAP.
Conclusion:
ACE genotyping is associated with blood pressure-lowering response to HCTZ. Specific genotypes might be associated with the response to specific antihypertensive treatment.
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