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Published on: May 26, 2022
Azelnidipine is a useful medication for the treatment of heart failure preserved ejection fraction
Shunsuke Kiuchi1, Shinji Hisatake1, Takayuki Kabuki1
1a Department of Cardiovascular Medicine , Toho University Faculty of Medicine , Tokyo , Japan.
Insights
Azelnidipine improved heart failure (HFpEF) severity and cardiac sympathetic nerve activity in patients with hypertension (HT) compared to cilnidipine. This study highlights azelnidipine
Area of Science:
- Cardiology
- Pharmacology
Background:
- Optimal therapy for heart failure with preserved ejection fraction (HFpEF) and hypertension (HT) remains unclear.
- Beta blockers (BB) and renin-angiotensin-aldosterone system inhibitors (RAAS-I) are recommended for HFpEF.
- Calcium channel blockers (CCBs) are also recommended for HFpEF, but the specific benefits of azelnidipine versus cilnidipine are not well-defined.
Purpose of the Study:
- To investigate the therapeutic differences between azelnidipine (L-type CCB) and cilnidipine (N-type CCB) in patients with HFpEF and HT.
- To evaluate the impact of switching from cilnidipine to azelnidipine on clinical and physiological markers.
Main Methods:
- A study involving 25 HFpEF patients concurrently treated with BB and RAAS-I.
- Patients initially received cilnidipine, then switched to azelnidipine for six months.
- Evaluated changes in blood pressure, heart rate, blood tests, echocardiography, and cardiac-scintigraphy (MIBG).
Main Results:
- No significant difference in blood pressure was observed between treatments.
- B-type natriuretic peptides significantly decreased, indicating improved HF severity (p=0.050).
- The MIBG washout rate significantly reduced, suggesting improved cardiac sympathetic nerve activity (p=0.011).
Conclusions:
- Azelnidipine demonstrated an improvement in heart failure severity compared to cilnidipine in hypertensive HFpEF patients.
- Azelnidipine also improved cardiac sympathetic nerve activity, as indicated by reduced MIBG washout rate.
- The findings suggest azelnidipine may offer additional benefits in managing hypertensive HFpEF patients.
Background:
The optimal therapy in patients with heart failure preserved ejection fraction (HFpEF) and hypertension (HT) has not been revealed. The beta blocker (BB) and the renin angiotensin aldosterone system inhibitor (RAAS-I) are recommend as class IIa in patients with HFpEF. The calcium channel blocker (CCB), a major anti-hypertensive drugs in Japan, is also recommend as class IIa in patients with HFpEF. However, the difference between azelnidipine, an L type CCB, and cilnidipine, an N type CCB, is unclear. We investigated the difference between azelnidipine and cilnidipine in patients with HFpEF and HT.
Methods:
Twenty-five consecutive HFpEF patients treated with BB and RAAS-I from April 2013 to March 2015 were enrolled. Initially, cilnidipine was used, and then switched to azelnidipine. Age, gender, blood pressure (BP), heart rate (HR), blood tests, echocardiography, and cardiac-scintigraphy (123I-metaiodobenzylguanidine: MIBG) were measured before and after six months from azelnidipine administration.
Results:
There was no statistically significant difference in BP. B type natriuretic peptides were significantly reduced (pre-state: 195.4 ± 209.7 pg/ml and post-state: 140.7 ± 136.4 pg/ml, p = 0.050). In echocardiography, the TEI index tended to be decreased (pre-state: 0.47 ± 0.15 and post-state: 0.42 ± 0.08, p = 0.057). As for MIBG, there was no significant change in the heart/mediastinum ratio. However, the washout rate was significantly reduced (pre-state: 44.7 ± 12.2 and post-state: 40.7 ± 12.1, p = 0.011). In addition, there was no statistically significant change, although HR tended to decrease by switching to azelnidipine (pre-state: 62.7 ± 11.6 and post-state: 61.8 ± 16.5, p = 0.373).
Conclusions:
In patients with HT and HFpEF, azelnidipine improved the severity of HF and cardiac sympathetic nerve activity compared with cilnidipine.
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