Efnodipine
Efnodipine
Efnodipine
www.jmscr.igmpublication.org
Index Copernicus Value: 79.54
ISSN (e)-2347-176x ISSN (p) 2455-0450
DOI: https://dx.doi.org/10.18535/jmscr/v7i2.56
Abstract
The role of efonidipine, a calcium channel blocker in reducing the progression of chronic renal disease is well
established by various studies. It also imparts beneficial effects in cardiovascular disease by reducing synthesis and
secretion of aldosterone, it prevents hypertrophy and remodelling of cardiac myocytes. There is decrease in 24 hour
urinary protein as efonidipine reduces glomerular capillary pressure. And overall there is improvement in GFR too.
The aim of the study is to find the role of efonidipine in CKD patients.
Methods: CKD patients (age >25 years, both gender) attending outdoor clinic and indoor CKD patients of Medicine
department Darbhanga Medical College were selected by simple random method and advised efonidipine 40mg once
daily. The statistical significance of improvement in proteinuria and GFR was measured.
Result: There was improvement in proteinuria in 52% patients taking efonidipine 40mg once daily. The GFR was
increased in 54% patients taking drug.
Out of 50 patients 29 were male and 21 were females. There was substantial decrease in 24 hour urinary protein in 26
patients out of 50 at the end of 6 months period. GFR also improved in 27 patients out of 50 at the end of study period.
Conclusion: Our 24 weeks study period in CKD patients taking efonidipine a novel dihydropyridine calcium antagonist
showed its beneficial effects. The outcome was measured by 24 hour urinary protein excretion and GFR. The beneficial
effect on proteinuria was particularly apparent in patients with proteinuria 1 g/day. These effects of efonidipine would
appear to make the drug more advantageous than other CCBs in terms of slowing the progression of renal dysfunction
and preventing cardiovascular tissue and organ injuries in patients with hypertension and chronic kidney disease.
There was improvement in proteinuria in 52% end of the study. The p value came to be .000
patients taking efonidipine 40mg once daily at the which was significant.
The GFR was calculated prior to the starting of CCB, dilates both the afferent and efferent
the study and at the end of the study. It was found arterioles in the isolated perfused kidney, while
that patients on efonidiopine 40mg daily the L-type CCB preferentially dilates the afferent
improved. The GFR was increased in 54% arterioles. The elevated glomerular hydraulic
patients taking drug. Statistically p value came to pressure promotes ultrafiltration of plasma
be significant. proteins, resulting in proteinuria.
It has been found in many large scale studies that
Discussion the amount of urinary protein excretion was
Diabetes and hypertension are leading causes of predictive for the rate of deterioration of renal
chronic renal failure worldwide. As we know function in patients with diabetic and non diabetic
these patients are also at risk of cardiovascular renal diseases. Proteinuria itself is detrimental to
complications. To prevent such complications the kidney because ultrafiltration of proteins
certain drugs which selectively improve the across the glomerular basement membrane brings
progression and improve the prognosis should be about mesangial and tubular protein overload,
used. which provokes inflammation and ultimately
To protect the kidneys from diabetic and other results in glomerulosclerosis and tubulo-
renal diseases, it is important to prevent the interstitial fibrosis. Proteinuria is also know to be
increase in glomerular capillary pressure. The a risk factor for cardiovascular disease.
drugs acting on rennin angiotensin system, such as Efonidipine, a dihydropirydine calcium channel
ACE inhibitors and ARBs, are known to improve blocker, has been shown to dilate the efferent
glomerular hypertension by reducing the glomerular arterioles as effectively as the afferent
constrictive effect of angiotensin II on the efferent arterioles. It increases glomerular filtration rate
arterioles. With regard to the Ca channels in the without increasing intra-glomerular pressure and
glomerular arterioles, the afferent arterioles filtration fraction. This prevents hypertension
express the L- and T-type Ca channels, while the induced renal damage. It also prevents Rho-
efferent arterioles express only the T-type Ca kinase induced renal parenchymal fibrosis and
channel. This distribution of Ca channels may provides long term renal protection.
explain the experimental observation that Efonidipine is unique among clinically available
efonidipine, the L- and T-type CCBs. Its antihypertensive efficacy is superior or
Dr U. C. Jha et al JMSCR Volume 07 Issue 02 February 2019 Page 300
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at par with other CCBs. But, in terms of Masanori FUJII1), Takashi
pleiotropic effects leading to enhanced cerebral, YAMAMOTO1), and Minoru HORIE1)
cardiac and renal protection, Efonidipine scores Comparison of the Effects of Efonidipine
over the other CCBs. and Amlodipine on Aldosterone in Patients
This study showed the effectiveness of efonidipine with Hypertension.
in providing renal protection in patients of chronic 5. Schulman NB, Ford CE, Hall WD,
renal failure. Blaufox MD, Simon D, Langford HG,
Schneider KA: Prognostic value of serum
Conclusion creatinine and effect of treatment of
A substantial proportion of patients advised hypertension on renal function: Results
efonidipine showed improvements in renal status. from the hypertension detection and
The reno protective benefits of efonidipine was follow-up program. Hypertension
imparted largely due to decrease in proteinuria 1989;13(Suppl 1):I-80–I-93.
and improvement in GFR. 6. Lewis EJ, Hunsicker LG, Bain RP, Rohde
RD, for the Collaborative Study Group:
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