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      Discrete Subaortic Stenosis: Perspective Roadmap to a Complex Disease

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          Abstract

          Discrete subaortic stenosis (DSS) is a congenital heart disease that results in the formation of a fibro-membranous tissue, causing an increased pressure gradient in the left ventricular outflow tract (LVOT). While surgical resection of the membrane has shown some success in eliminating the obstruction, it poses significant risks associated with anesthesia, sternotomy, and heart bypass, and it remains associated with a high rate of recurrence. Although a genetic etiology had been initially proposed, the association between DSS and left ventricle (LV) geometrical abnormalities has provided more support to a hemodynamic etiology by which congenital or post-surgical LVOT geometric derangements could generate abnormal shear forces on the septal wall, triggering in turn a fibrotic response. Validating this hypothetical etiology and understanding the mechanobiological processes by which altered shear forces induce fibrosis in the LVOT are major knowledge gaps. This perspective paper describes the current state of knowledge of DSS, articulates the research needs to yield mechanistic insights into a significant pathologic process that is poorly understood, and proposes several strategies aimed at elucidating the potential mechanobiological synergies responsible for DSS pathogenesis. The proposed roadmap has the potential to improve DSS management by identifying early targets for prevention of the fibrotic lesion, and may also prove beneficial in other fibrotic cardiovascular diseases associated with altered flow.

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          Most cited references100

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          Effects of shear stress on endothelial cells: go with the flow.

          Haemodynamic forces influence the functional properties of vascular endothelium. Endothelial cells (ECs) have a variety of receptors, which sense flow and transmit mechanical signals through mechanosensitive signalling pathways to recipient molecules that lead to phenotypic and functional changes. Arterial architecture varies greatly exhibiting bifurcations, branch points and curved regions, which are exposed to various flow patterns. Clinical studies showed that atherosclerotic plaques develop preferentially at arterial branches and curvatures, that is in the regions exposed to disturbed flow and shear stress. In the atheroprone regions, the endothelium has a proinflammatory phenotype associated with low nitric oxide production, reduced barrier function and increased proadhesive, procoagulant and proproliferative properties. Atheroresistant regions are exposed to laminar flow and high shear stress that induce prosurvival antioxidant signals and maintain the quiescent phenotype in ECs. Indeed, various flow patterns contribute to phenotypic and functional heterogeneity of arterial endothelium whose response to proatherogenic stimuli is differentiated. This may explain the preferential development of endothelial dysfunction in arterial sites with disturbed flow.
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            Vascular endothelium, hemodynamics, and the pathobiology of atherosclerosis.

            The localization of atherosclerotic lesion formation to regions of disturbed blood flow associated with certain arterial geometries, in humans and experimental animals, suggests an important role for hemodynamic forces in the pathobiology of atherosclerosis. There is increasing evidence that the vascular endothelium, which is directly exposed to various fluid mechanical forces generated by pulsatile blood flow, can discriminate among these different biomechanical stimuli and transduce them into genetic regulatory programs that modulate endothelial function. In this brief review, we discuss how biomechanical stimuli generated by blood flow can influence endothelial functional phenotypes, and explore the working hypothesis of "atheroprone" hemodynamic environments as "local risk factors" in atherogenesis. In addition, we consider the therapeutic implications of the activation of "atheroprotective genes" and their role as "critical regulatory nodes" in vascular homeostasis. Copyright © 2013 Elsevier Inc. All rights reserved.
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              Complex hemodynamics at the apex of an arterial bifurcation induces vascular remodeling resembling cerebral aneurysm initiation.

              Arterial bifurcation apices are common sites for cerebral aneurysms, raising the possibility that the unique hemodynamic conditions associated with flow dividers predispose the apical vessel wall to aneurysm formation. This study sought to identify the specific hemodynamic insults that lead to maladaptive vascular remodeling associated with aneurysm development and to identify early remodeling events at the tissue and cellular levels. We surgically created new branch points in the carotid vasculature of 6 female adult dogs. In vivo angiographic imaging and computational fluid dynamics simulations revealed the detailed hemodynamic microenvironment for each bifurcation, which were then spatially correlated with histologic features showing specific tissue responses. We observed 2 distinct patterns of vessel wall remodeling: (1) hyperplasia that formed an intimal pad at the bifurcation apex and (2) destructive remodeling in the adjacent region of flow acceleration that resembled the initiation of an intracranial aneurysm, characterized by disruption of the internal elastic lamina, loss of medial smooth muscle cells, reduced proliferation of smooth muscle cells, and loss of fibronectin. Strong localization of aneurysm-type remodeling to the region of accelerating flow suggests that a combination of high wall shear stress and a high gradient in wall shear stress represents a "dangerous" hemodynamic condition that predisposes the apical vessel wall to aneurysm formation.
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                Author and article information

                Contributors
                Journal
                Front Cardiovasc Med
                Front Cardiovasc Med
                Front. Cardiovasc. Med.
                Frontiers in Cardiovascular Medicine
                Frontiers Media S.A.
                2297-055X
                13 September 2018
                2018
                : 5
                : 122
                Affiliations
                [1] 1Department of Mechanical and Materials Engineering, Wright State University , Dayton, OH, United States
                [2] 2Department of Bioengineering, Rice University , Houston, TX, United States
                [3] 3Division of Pediatric Surgery, Texas Children's Hospital , Houston, TX, United States
                [4] 4Department of Surgery, Baylor College of Medicine , Houston, TX, United States
                Author notes

                Edited by: Umberto Morbiducci, Politecnico di Torino, Italy

                Reviewed by: Marcus Kelm, Deutsches Herzzentrum Berlin, Germany; Fabrizio D'Ascenzo, San Giovanni Battista Molinette, Italy

                *Correspondence: Philippe Sucosky philippe.sucosky@ 123456wright.edu

                This article was submitted to Pediatric Cardiology, a section of the journal Frontiers in Cardiovascular Medicine

                Article
                10.3389/fcvm.2018.00122
                6166095
                30320123
                15f528fd-6f48-4001-bf35-0dbf951640fe
                Copyright © 2018 Massé, Shar, Brown, Keswani, Grande-Allen and Sucosky.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 20 June 2018
                : 17 August 2018
                Page count
                Figures: 2, Tables: 0, Equations: 0, References: 113, Pages: 9, Words: 7063
                Funding
                Funded by: National Institutes of Health 10.13039/100000002
                Award ID: R01HL140305
                Funded by: Division of Civil, Mechanical and Manufacturing Innovation 10.13039/100000147
                Award ID: CMMI-1550144
                Funded by: American Heart Association 10.13039/100000968
                Award ID: 17GRNT33350028
                Categories
                Cardiovascular Medicine
                Perspective

                discrete subaortic stenosis,congenital heart disease,hemodynamics,etiology,left ventricular outflow tract,wall shear stress,aortoseptal angle

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