Shinya Fukumoto, Eiji Ishimura, Koka Motoyama, Tomoaki Morioka, Eiji Kimoto, Ken Wakikawa, Shigeichi Shoji, Hidenori Koyama, Tetsuo Shoji, Masanori Emoto, Yoshiki Nishizawa, Masaaki Inaba
Index: Diabetes Res. Clin. Pract. 97(1) , 91-8, (2012)
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We evaluated the antialbuminuric advantage of cilnidipine, an N/L-type calcium channel blocker (CCB), compared with L-type CCBs in diabetic patients with normoalbuminuria and microalbuminuria. The study was a multicenter, non-randomized crossover trial. Participants were 90 type 2 diabetic patients exhibiting either normo- or microalbuminuria, and undergoing CCB treatment for ≥6 months prior to study entry. The CCB at the time of entry was continued for the first 6 months (Period 1). Treatment was subsequently switched from cilnidipine to an L-type CCB, or vice versa, for the second 6-month observation period (Period 2). During Period 1, the L-type CCB group showed a significant increase of urinary albumin excretion (UAE) over time, while the cilnidipine group showed no significant elevation. During Period 2, switching of the treatment from the L-type CCB to cilnidipine resulted in significant reduction of the UAE, whereas switching from cilnidipine to the L-type CCB resulted in no significant change in the UAE. This study demonstrated that the antialbuminuric effect of Cilnidipine, but not the L-type CCBs, was sustained even in patients treated for a long time. In addition, the antialbuminuric effect can be anticipated after switching from an L-type CCB to cilnidipine, but not vice versa.Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.
Structure | Name/CAS No. | Molecular Formula | Articles |
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Cilnidipine
CAS:132203-70-4 |
C27H28N2O7 |
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