Key result
Amlodipine demonstrated similar effects on renal parameters compared to newer calcium channel blockers, but showed higher potency by achieving greater blood pressure reduction at a lower dose.
Why the study?
Studying the effect of dihydropyridine CCBs on renal outcomes, specifically for amlodipine monotherapy in real-world settings, can help expand its usage among Indian patients.
Does amlodipine compared to other dihydropyridine CCBs improve renal parameters and blood pressure in adult Indian patients with essential hypertension?
Observational (n=324)
Yes
Does amlodipine compared to other dihydropyridine CCBs improve renal parameters and blood pressure in adult Indian patients with essential hypertension?
Amlodipine demonstrated similar renoprotective effects and greater blood pressure reduction per mg dose compared to newer dihydropyridine CCBs in Indian patients with essential hypertension.
Answers are grounded in this paper and cite their sources.
Similar renal effects across CCBs with greater per-dose BP reduction for amlodipine; leaves open randomized confirmation before practice change.
INTRODUCTION: The renoprotective effects of dihydropyridine calcium channel blockers (CCBs) have been established as non-inferior to other classes of antihypertensive drugs. Studying their effect on renal outcome parameters, specifically for amlodipine as monotherapy, in real-world settings can further help in expanding its usage among Indian patients. This study was performed to assess the effects of amlodipine and other dihydropyridine CCBs (cilnidipine, benidipine and azelnidipine) on renal parameters and effectiveness in blood pressure reduction in Indian patients. METHODS: The retrospective data of adult patients (> 18 years) with essential hypertensive who were prescribed amlodipine (n = 92), cilnidipine (n = 91), benidipine (n = 70) or azelnidipine (n = 71) as monotherapy were analyzed. The renal outcomes, serum creatinine, estimated glomerular filtration rate (eGFR), blood urea nitrogen (BUN), microalbumin, urine albumin-to-creatinine ratio (UACR), sodium and potassium levels, and mean changes in BP were analyzed from baseline to 12 months. Appropriate statistical methods were used to determine the significance (p value < 0.05). RESULTS: From baseline to the end of the study, mean serum creatinine changed from 0.98 ± 0.17 to 1.07 ± 0.28 mg/dL with amlodipine, 0.97 ± 0.18 to 1.13 ± 0.50 mg/dL with cilnidipine, 0.98 ± 0.30 to 0.97 ± 0.27 mg/dL wi th benidipine, and 0.99 ± 0.23 to 0.98 ± 0.25 mg/dL with azelnidipine (p = 0.01). The mean microalbumin and UACR were reduced from baseline to the end of the study (p = 0.06 and p > 0.05). No significant changes were observed in BUN, sodium or potassium levels. Overall, for all CCBs, the mean systolic blood pressure (SBP) and diastolic blood pressure (DBP) values were reduced from baseline to the end of the study (p = 0.002). At the end of the study, the average dose of amlodipine was 7.25 mg, and the average reduction in SBP and DBP per mg dose was 1.54 and 0.57 mmHg. The corresponding numbers for the other CCBs were as follows: cilnidipine, 14.28 mg, 0.26 and 0.01; benidipine, 5.71 mg, 0.41 and 0.11; azelnidipine, 15.88 mg, 0.13 and 0.06. CONCLUSION: Amlodipine and other CCBs demonstrated good efficacy and similar effects on renal parameters from baseline to end of study. Amlodipine also showed higher potency by demonstrating greater BP reduction at a lower dose. Thus, amlodipine can remain a preferred choice among CCBs, even with the advent of the newer CCBs.
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Jadhav et al. (2021) conducted an observational in Essential Hypertension (n=324). Amlodipine vs. Cilnidipine, benidipine, or azelnidipine was evaluated on Mean serum creatinine at end of study (mg/dL) (p=0.01). Amlodipine demonstrated similar effects on renal parameters compared to newer calcium channel blockers, but showed higher potency by achieving greater blood pressure reduction at a lower dose.
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