Switching to an L/N-Type Calcium Channel Blocker Shows Renoprotective Effects in Patients with Chronic Kidney Disease: The Kyoto Cilnidipine Study

Author:

Hatta T1,Takeda K2,Shiotsu Y1,Sugishita C3,Adachi T1,Kimura T3,Sonomura K3,Kusaba T4,Kishimioto N1,Narumiya H5,Tanda S6,Tamagaki K7,Yamada K8,Kameyama H1,Kido H6,Harada S2,Bito Y9,Moriguchi J2,Morimoto S10,Okigaki M1,Itoh H2,Mori Y3,Nakata T11,Maki K1,Sasaki S6,Sawada K1,Matsubara H3

Affiliation:

1. Department of Medicine, Division of Hypertension and Nephrology and Kidney Centre, Omihachiman Community Medical Centre, Shiga, Japan

2. Kyoto Industrial Health Association, Kyoto, Japan

3. Department of Medicine, Division of Hypertension and Nephrology, Kyoto Prefectural University of Medicine, Kyoto, Japan

4. Department of Medicine, Division of Nephrology, Nantan Hospital, Kyoto, Japan

5. Department of Medicine, Kyoto Second Red Cross Hospital, Kyoto, Japan

6. Department of Medicine, Akashi City Hospital, Hyogo, Japan

7. Department of Medicine, Division of Nephrology, St Luke's International Hospital, Tokyo, Japan

8. Department of Medicine, Division of Nephrology and Dialysis, Kameoka Shimizu Hospital, Kyoto, Japan

9. Sannomiya Clinic, Hyogo, Japan

10. Department of Medicine, Kansai Medical University, Osaka, Japan

11. Kyoto Pharmaceutical University, Kyoto, Japan

Abstract

OBJECTIVE: This open-label, randomized controlled trial investigated the effects of cilnidipine, an L/N-type calcium channel blocker (CCB), in patients with chronic kidney disease (CKD). METHODS: Sixty patients with CKD and well-controlled hypertension being treated with a renin—angiotensin system (RAS) inhibitor and an L-type CCB (L-CCB) were randomly assigned either to switch from the L-CCB to cilnidipine after a 4-week observation period or to continue with L-CCB treatment. Blood pressure, heart rate and renal function were monitored for 12 months. Data were available for analysis from 50 patients: 24 from the cilnidipine group and 26 from the L-CCB group. RESULTS: Blood pressure was well controlled in both groups. After 12 months, proteinuria and heart rate were significantly decreased in the cilnidipine group, but proteinuria increased and heart rate remained unchanged in the L-CCB group. There was a significant positive correlation between the percentage changes in proteinuria and heart rate. CONCLUSIONS: Cilnidipine has antihypertensive effects equivalent to those of L-CCBs. In patients with CKD, proteinuria can be decreased by switching from an L-CCB to cilnidipine, thereby improving renal function.

Publisher

SAGE Publications

Subject

Biochemistry (medical),Cell Biology,Biochemistry,General Medicine

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