Key result
Lercanidipine 20 mg/d significantly decreased activated MMP-9 in hypertensive patients without (95% CI, -47 to -19%; P=0.047) and with diabetes (95% CI, -96 to -80%; P=0.010).
Why the study?
Does lercanidipine reduce MMP-9 activity and oxidative stress in hypertensive patients?
RCT (n=32)
Single-blind
Crossover
Does lercanidipine reduce MMP-9 activity and oxidative stress in hypertensive patients?
Lercanidipine reduces oxidative stress and MMP-9 activity in hypertensive patients regardless of diabetes status, suggesting pleiotropic vascular benefits beyond blood pressure lowering.
Lercanidipine may confer pleiotropic vascular benefits via MMP-9 reduction independent of BP effects; extends mechanistic RCT evidence in hypertension with or without diabetes.
Increased levels of metalloproteinase (MMP)-9 have been shown in hypertensive patients. Lercanidipine is a calcium channel blocker with antioxidant actions. We examined whether lercanidipine produces antioxidant effects and reduces MMP-9 activity in hypertensive patients in a placebo-controlled, crossover, single-blinded design study including 18 healthy volunteers (control group), and 14 hypertensive patients without (N = 7) or with (N = 7) diabetes mellitus. Hypertensive patients were randomized to treatment with placebo (15 days) or lercanidipine 20 mg/d (15 days). Arterial blood pressure was evaluated with ambulatory blood pressure monitoring. Plasma thiobarbituric acid reactive species (TBA-RS) levels were measured to assess oxidative stress, and plasma MMP-2 and MMP-9 were assayed by gel zymography before and after treatment with placebo or lercanidipine. Plasma concentrations of tissue inhibitor of metalloproteinases (TIMP)-1 were measured by ELISA. Lercanidipine reduced mean arterial pressure by 7% in hypertensive patients without diabetes (P < 0.05), but not in hypertensive patients with diabetes. It significantly decreased plasma TBA-RS levels in hypertensive patients without and with diabetes (95% confidence interval [CI], -26 to -46%, P = 0.048, and -22 to -33%, P = 0.036, respectively). In addition, lercanidipine decreased activated MMP-9 in hypertensive patients without and with diabetes (95% CI, -19 to -47%, P = 0.047, and -80 to -96%, P = 0.010, respectively). No effects were seen on MMP-2. No significant differences or changes in plasma TIMP-1 concentrations were found. Therefore, we demonstrate for the first time that lercanidipine consistently decreased MMP-9 activity and reduced oxidative stress in hypertensive patients, thus suggesting a mechanism probably involved in the pleotropic actions of lercanidipine.
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Martinez et al. (2006) conducted an RCT in Hypertension (n=32). Lercanidipine vs. Placebo was evaluated on Activated MMP-9 in hypertensive patients without diabetes (95% CI -47 to -19%, p=0.047). Lercanidipine 20 mg/d significantly decreased activated MMP-9 in hypertensive patients without (95% CI, -47 to -19%; P=0.047) and with diabetes (95% CI, -96 to -80%; P=0.010).
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