The Promise of Cilnidipine in Hypertension with Comorbidities: National Consensus Statement
dc.contributor.author | Chopra H.K. | |
dc.contributor.author | Wander G.S. | |
dc.contributor.author | Ponde C.K. | |
dc.contributor.author | Nanda N.C. | |
dc.contributor.author | Khullar D. | |
dc.contributor.author | Venugopal K. | |
dc.contributor.author | Ray S. | |
dc.contributor.author | Nair T. | |
dc.contributor.author | Rana D.S. | |
dc.contributor.author | Kher V. | |
dc.contributor.author | Sawhney J.P.S. | |
dc.contributor.author | Kasliwal R.R. | |
dc.contributor.author | Abdullakutty J. | |
dc.contributor.author | Chakraborty R. | |
dc.contributor.author | Chandra P. | |
dc.contributor.author | Bansal S. | |
dc.contributor.author | Kumar V. | |
dc.contributor.author | Pancholia A.K. | |
dc.contributor.author | Kapoor A. | |
dc.contributor.author | Prakash S. | |
dc.contributor.author | Saxena A. | |
dc.contributor.author | Rastogi V. | |
dc.contributor.author | Sharma V. | |
dc.contributor.author | Arora Y.K. | |
dc.contributor.author | Dasbiswas A. | |
dc.contributor.author | Bhargava M. | |
dc.contributor.author | Jaswal A. | |
dc.contributor.author | Bhargava K. | |
dc.contributor.author | Bhatia M. | |
dc.contributor.author | Omar A.K. | |
dc.contributor.author | Khanna N.N. | |
dc.contributor.author | Passey R. | |
dc.contributor.author | Bhalla D. | |
dc.contributor.author | Vijayalakshmi I.B. | |
dc.contributor.author | Bhalla A.K. | |
dc.contributor.author | Moorthy A. | |
dc.contributor.author | Isser H.S. | |
dc.contributor.author | Mishra S.S. | |
dc.contributor.author | Routray S. | |
dc.contributor.author | Tandon V. | |
dc.contributor.author | Sinha A. | |
dc.contributor.author | Bansal M. | |
dc.contributor.author | Jain P. | |
dc.contributor.author | Hotchandani R. | |
dc.contributor.author | Jain D. | |
dc.contributor.author | Katyal V.K. | |
dc.contributor.author | Gulati S. | |
dc.contributor.author | Tandon R. | |
dc.contributor.author | Jaggi S. | |
dc.contributor.author | Sehgal B. | |
dc.contributor.author | Gupta V. | |
dc.contributor.author | Mehrotra R. | |
dc.contributor.author | Krishnamani N.C. | |
dc.contributor.author | Pathak S.N. | |
dc.contributor.author | Yadav M.S. | |
dc.contributor.author | Chawla R. | |
dc.contributor.author | Shastry N.R. | |
dc.contributor.author | Chatterjee N. | |
dc.contributor.author | Samajdar S.S. | |
dc.contributor.author | Pal J. | |
dc.contributor.author | Tiwaskar M. | |
dc.date.accessioned | 2025-01-13T07:09:02Z | |
dc.date.available | 2025-01-13T07:09:02Z | |
dc.date.issued | 2024 | |
dc.description.abstract | The 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.doi | 10.59556/japi.71.0400 | |
dc.identifier.issn | 45772 | |
dc.identifier.uri | https://dl.bhu.ac.in/ir/handle/123456789/3490 | |
dc.language.iso | en | |
dc.publisher | Journal of Association of Physicians of India | |
dc.title | The Promise of Cilnidipine in Hypertension with Comorbidities: National Consensus Statement | |
dc.type | Article | |
journal.title | Journal of Association of Physicians of India | |
journalvolume.identifier.volume | 72 |