Literature DB >> 31040188

Arterial Stiffness in the Heart Disease of CKD.

Luca Zanoli1, Paolo Lentini2, Marie Briet3, Pietro Castellino4, Andrew A House5, Gerard M London6, Lorenzo Malatino4, Peter A McCullough7, Dimitri P Mikhailidis8, Pierre Boutouyrie6,9,10.   

Abstract

CKD frequently leads to chronic cardiac dysfunction. This complex relationship has been termed as cardiorenal syndrome type 4 or cardio-renal link. Despite numerous studies and reviews focused on the pathophysiology and therapy of this syndrome, the role of arterial stiffness has been frequently overlooked. In this regard, several pathogenic factors, including uremic toxins (i.e., uric acid, phosphates, endothelin-1, advanced glycation end-products, and asymmetric dimethylarginine), can be involved. Their effect on the arterial wall, direct or mediated by chronic inflammation and oxidative stress, results in arterial stiffening and decreased vascular compliance. The increase in aortic stiffness results in increased cardiac workload and reduced coronary artery perfusion pressure that, in turn, may lead to microvascular cardiac ischemia. Conversely, reduced arterial stiffness has been associated with increased survival. Several approaches can be considered to reduce vascular stiffness and improve vascular function in patients with CKD. This review primarily discusses current understanding of the mechanisms concerning uremic toxins, arterial stiffening, and impaired cardiac function, and the therapeutic options to reduce arterial stiffness in patients with CKD.
Copyright © 2019 by the American Society of Nephrology.

Entities:  

Keywords:  arteries, cardiovascular disease, chronic kidney disease, Chronic inflammation, arteriosclerosis, pulse wave velocity

Mesh:

Substances:

Year:  2019        PMID: 31040188      PMCID: PMC6551785          DOI: 10.1681/ASN.2019020117

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  114 in total

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Review 2.  Mechanisms, pathophysiology, and therapy of arterial stiffness.

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Review 7.  mTOR inhibition: a promising strategy for stabilization of atherosclerotic plaques.

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8.  Asymmetric dimethylarginine causes hypertension and cardiac dysfunction in humans and is actively metabolized by dimethylarginine dimethylaminohydrolase.

Authors:  Vinod Achan; Michael Broadhead; Mohammed Malaki; Guy Whitley; James Leiper; Raymond MacAllister; Patrick Vallance
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Journal:  Medicine (Baltimore)       Date:  2016-01       Impact factor: 1.817

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  35 in total

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10.  Changes in Blood Pressure and Arterial Hemodynamics following Living Kidney Donation.

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