Key result
Switching from L-type CCBs to benidipine reduces UACR by ~37% in hypertensive patients.
Why the study?
Albuminuria and high plasma aldosterone concentration predict poor cardiovascular outcomes, but the effects of the T/L-type calcium channel blocker benidipine on these markers required investigation.
Does switching from an L-type CCB to benidipine reduce albuminuria and plasma aldosterone concentration in patients with controlled essential hypertension?
Does switching from an L-type CCB to benidipine reduce albuminuria and plasma aldosterone concentration in patients with controlled essential hypertension?
Effect estimate: -36.9% median change
Absolute Event Rate: 19.6% vs 33.5%
p-value: p=0.001
Switching from an L-type CCB to the T/L-type CCB benidipine in hypertensive patients maintains blood pressure control while significantly reducing albuminuria and plasma aldosterone concentration.
Should not yet change CCB prescribing in hypertension; leaves open whether benidipine confers renoprotective benefit beyond L-type agents.
Albuminuria and a high plasma aldosterone concentration (PAC) are prognosis factors predicting a poor outcome for cardiovascular disease. We examined here the effects of benidipine, a T/L-type calcium channel blocker (CCB), on albuminuria and PAC.Thirty-one patients with essential hypertension who received an L-type CCB and achieved the target blood pressure (BP) indicated by the Treatment Guidelines of the Japan Society of Hypertension (JSH2009) were investigated. The Ltype CCB under treatment was switched to benidipine at a dose in which equivalent BP reduction was expected. BP and estimated glomerular filtration rate at 6 months after switching to benidipine were not significantly different from those at baseline. The urinary-albumin-creatinine ratio (UACR) decreased significantly by 36.9% (P = 0.001). No significant change was observed in plasma renin activity (P = 0.063). The PAC of all patients decreased significantly by 11.8% (P = 0.002). When analyzed by daily doses of benidipine, the PAC appeared to have decreased in patients who received 4 mg per day of benidipine (n = 14), although statistical significance was not reached (P = 0.096). The PAC in patients who received 8 mg per day of benidipine (n =17) was significantly reduced by 13.2% (P = 0.017).In hypertensive patients whose BP is controlled by L-type CCB, switching to the T/L-type CCB benidipine maintained BP control and reduced UACR. In addition, the high dose of benidipine reduced the PAC independent of BP control. These results suggest the T/L-type CCB benidipine may contribute to cardio-renal protection in addition to lowering BP.
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Tani et al. (2014) studied Essential hypertension (n=31). Benidipine vs. Baseline (L-type CCB) was evaluated on Change in urinary albumin-to-creatinine ratio (UACR) at 6 months (-36.9% median change, p=0.001). Switching from an L-type calcium channel blocker to benidipine significantly reduced the urinary albumin-to-creatinine ratio by 36.9% and plasma aldosterone concentration by 11.8% in hypertensive patients.
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