Title:
The Promise of Cilnidipine in Hypertension with Comorbidities: National Consensus Statement

dc.contributor.authorHirday Kumar Chopra
dc.contributor.authorGurpreet S. Wander
dc.contributor.authorChandrashekhar K. Ponde
dc.contributor.authorNavin C. Nanda
dc.contributor.authorDinesh Khullar
dc.contributor.authorK. Venugopal
dc.contributor.authorSaumitra Ray
dc.contributor.authorTiny Nair
dc.contributor.authorD.S. Rana
dc.contributor.authorVijay Kher
dc.contributor.authorJ.P.S. Sawhney
dc.contributor.authorR.R. Kasliwal
dc.contributor.authorJabir Abdullakutty
dc.contributor.authorRabin Chakraborty
dc.contributor.authorPraveen Chandra
dc.contributor.authorSandeep Bansal
dc.contributor.authorViveka Kumar
dc.contributor.authorArvind K. Pancholia
dc.contributor.authorAditya Kapoor
dc.contributor.authorSunil Prakash
dc.contributor.authorAnil Saxena
dc.contributor.authorVishal Rastogi
dc.contributor.authorVinod Sharma
dc.contributor.authorY.K. Arora
dc.contributor.authorArup Dasbiswas
dc.contributor.authorMohan Bhargava
dc.contributor.authorAparna Jaswal
dc.contributor.authorKartikeya Bhargava
dc.contributor.authorMona Bhatia
dc.contributor.authorAshok K. Omar
dc.contributor.authorNarendra Nath Khanna
dc.contributor.authorRajiv Passey
dc.contributor.authorDilip Bhalla
dc.contributor.authorI.B. Vijayalakshmi
dc.contributor.authorAnil Kumar Bhalla
dc.contributor.authorAsha Moorthy
dc.contributor.authorHarmohander S. Isser
dc.contributor.authorS.S. Mishra
dc.contributor.authorSatyanarayan Routray
dc.contributor.authorVivek Tandon
dc.contributor.authorAjay Sinha
dc.contributor.authorManish Bansal
dc.contributor.authorPraveen Jain
dc.contributor.authorRamesh Hotchandani
dc.contributor.authorDharmendra Jain
dc.contributor.authorV.K. Katyal
dc.contributor.authorSanjiv Gulati
dc.contributor.authorRohit Tandon
dc.contributor.authorShalini Jaggi
dc.contributor.authorBlessy Sehgal
dc.contributor.authorVitull Gupta
dc.contributor.authorRahul Mehrotra
dc.contributor.authorN.C. Krishnamani
dc.contributor.authorS.N. Pathak
dc.contributor.authorM.S. Yadav
dc.contributor.authorRajeev Chawla
dc.contributor.authorN.R. Shastry
dc.contributor.authorNandini Chatterjee
dc.contributor.authorShambo Samrat Samajdar
dc.contributor.authorJyotirmoy Pal
dc.contributor.authorMangesh Tiwaskar
dc.date.accessioned2026-02-09T04:44:14Z
dc.date.issued2024
dc.description.abstractThe rapidly increasing burden of hypertension is responsible for premature deaths from cardiovascular disease (CVD), renal disease, and stroke, with a tremendous public health and financial burden. Hypertension detection, treatment, and control vary worldwide; it is still low, particularly in low- and middle-income countries (LMICs). High blood pressure (BP) and CVD risk have a strong, linear, and independent association. They contribute to alarming numbers of all-cause and CVD deaths. A major culprit for increased hypertension is sympathetic activity, and further complications of hypertension are heart failure, ischemic heart disease (IHD), stroke, and renal failure. Now, antihypertensive interventions have emerged as a global public health priority to reduce BP-related morbidity and mortality. Calcium channel blockers (CCB) are highly effective vasodilators. and the most common drugs used for managing hypertension and CVD. Cilnidipine, with both L- and N-type calcium channel blocking activity, is a promising 4th generation CCB. It causes vasodilation via L-type calcium channel blockade and inhibits the sympathetic nervous system (SNS) via N-type calcium channel blockade. Cilnidipine, which acts as a dual L/N-type CCB, is linked to a reduced occurrence of pedal edema compared to amlodipine, which solely blocks L-type calcium channels. The antihypertensive properties of cilnidipine are very substantial, with low BP variability and long-acting properties. It is beneficial for hypertensive patients to deal with morning hypertension and for patients with abnormal nocturnal BP due to exaggerated sympathetic nerve activation. Besides its BP-lowering effect, it also exhibits organ protection via sympathetic nerve inhibition and renin–angiotensin–aldosterone system inhibition; it controls heart rate and proteinuria. Reno-protective, neuroprotective, and cardioprotective effects of cilnidipine have been well-documented and demonstrated. © 2024 Journal of Association of Physicians of India. All rights reserved.
dc.identifier.doi10.59556/japi.71.0400
dc.identifier.issn45772
dc.identifier.urihttps://doi.org/10.59556/japi.71.0400
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/49658
dc.publisherJournal of Association of Physicians of India
dc.titleThe Promise of Cilnidipine in Hypertension with Comorbidities: National Consensus Statement
dc.typePublication
dspace.entity.typeArticle

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