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Effect of a calcium-channel blocker and β-blocker combination on reading-to-reading blood pressure variability: a
Jia-Hui Xia1, Yi-Bang Cheng, Ting-Yan Xu
1Department of Cardiovascular Medicine, Centre for Epidemiological Studies and Clinical Trials, State Key Laboratory of Medical Genomics, Shanghai Key Laboratory of Hypertension, Shanghai Institute of Hypertension, National Research Centre for Translational Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Insights
The nitrendipine/atenolol combination effectively reduced blood pressure and daytime blood pressure variability. However, it did not demonstrate superiority over individual nitrendipine or atenolol treatments for hypertension management.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Hypertension management often involves combination therapy to achieve optimal blood pressure control.
- Blood pressure variability (BPV) is an emerging risk factor for cardiovascular events.
- Assessing BPV using ambulatory blood pressure monitoring (ABPM) provides valuable insights into treatment efficacy.
Purpose of the Study:
- To compare the efficacy of a nitrendipine/atenolol combination with monotherapy using standard doses of either drug.
- To evaluate the impact of these treatments on both blood pressure (BP) and blood pressure variability (BPV).
- To assess BP and BPV using ambulatory blood pressure monitoring.
Main Methods:
- A randomized, crossover trial involving 32 patients (30-65 years) with grade 1 hypertension and elevated daytime BPV.
- Patients received either the nitrendipine/atenolol combination (10/20 mg) or monotherapy (nitrendipine 10 mg or atenolol 25 mg) for 6 weeks, followed by a crossover.
- Ambulatory blood pressure monitoring was used to assess BP and BPV.
Main Results:
- The nitrendipine/atenolol combination significantly reduced clinic and ambulatory BP and pulse rate from baseline.
- Significant reductions in 24-hour and daytime systolic and diastolic BPV were observed with the combination therapy.
- No significant differences in BPV were found between the combination and monotherapy groups at the end of treatment.
Conclusions:
- The nitrendipine/atenolol combination effectively reduced daytime reading-to-reading blood pressure variability.
- The combination therapy did not demonstrate superiority over standard-dose nitrendipine or atenolol monotherapy in overall efficacy.
- Further research may be needed to fully elucidate the role of combination therapy in managing BPV.
Objective:
The objective of this study was to investigate the efficacy of the nitrendipine/atenolol combination in comparison with standard-dose nitrendipine or atenolol monotherapy in reducing blood pressure (BP) and blood pressure variability (BPV) as assessed by ambulatory BP monitoring.
Methods:
In a randomized, crossover trial, 32 patients (30-65 years) with grade 1 hypertension and elevated daytime reading-to-reading BPV were randomly assigned to receive either the nitrendipine/atenolol combination (10/20 mg) or standard-dose nitrendipine (10 mg) or atenolol (25 mg) monotherapy for 6 weeks, followed by a crossover to another treatment for 6 weeks.
Results:
The final analysis included 31 patients (mean [±SD] age, 49.2 ± 9.6 years) and 12 men. The nitrendipine/atenolol combination significantly reduced from baseline clinic and ambulatory BP and pulse rate ( P ≤ 0.002), and 24 h and daytime systolic and diastolic BPV as assessed by SD and average real variability ( P ≤ 0.042), but not the coefficient of variation nor nighttime BPV indices ( P ≥ 0.06). Significant differences between the nitrendipine/atenolol combination and nitrendipine or atenolol monotherapy at the end of treatment were observed in clinic BP and pulse rate ( P ≤ 0.042), but not in 24 h, daytime and nighttime blood pressure and pulse rate, except for daytime DBP and 24 h and daytime pulse rate ( P ≤ 0.049). There were no significant differences in BPV between the combination and monotherpy groups at the end of treatment ( P ≥ 0.25).
Conclusion:
The nitrendipine/atenolol combination reduced daytime reading-to-reading BPV, but did not show superiority to nitrendipine or atenolol monotherapy.
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