Arterial Wall Properties and Womersley Flow in Fabry Disease

<p>Abstract</p> <p>Background</p> <p>Fabry disease is an X-linked recessive lysosomal storage disease resulting in the cellular accumulation of globotriaosylceramide particularly globotriaosylceramide. The disease is characterized by a dilated vasculopathy with arterial...

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Main Authors: Dimitriadis Emilios, Campia Umberto, Panza Julio A, Pursley Randall, Altarescu Gheona, Moore David F, Schiffmann Raphael
Format: Article
Language:English
Published: BMC 2002-01-01
Series:BMC Cardiovascular Disorders
Online Access:http://www.biomedcentral.com/1471-2261/2/1
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spelling doaj-4cfc39b89a82438c96c1db25a61b0f3a2020-11-25T01:42:42ZengBMCBMC Cardiovascular Disorders1471-22612002-01-0121110.1186/1471-2261-2-1Arterial Wall Properties and Womersley Flow in Fabry DiseaseDimitriadis EmiliosCampia UmbertoPanza Julio APursley RandallAltarescu GheonaMoore David FSchiffmann Raphael<p>Abstract</p> <p>Background</p> <p>Fabry disease is an X-linked recessive lysosomal storage disease resulting in the cellular accumulation of globotriaosylceramide particularly globotriaosylceramide. The disease is characterized by a dilated vasculopathy with arterial ectasia in muscular arteries and arterioles. Previous venous plethysomographic studies suggest enhanced endothelium-dependent vasodilation in Fabry disease indicating a functional abnormality of resistance vessels.</p> <p>Methods</p> <p>We examined the mechanical properties of the radial artery in Fabry disease, a typical fibro-muscular artery. Eight control subjects and seven patients with Fabry disease had a right brachial arterial line placed allowing real time recording of intra-arterial blood pressure. Real time B-mode ultrasound recordings of the right radial artery were obtained simultaneously allowing calculation of the vessel wall internal and external diameter, the incremental Young's modulus and arterial wall thickness. By simultaneously measurement of the distal index finger-pulse oximetry the pulse wave speed was calculated. From the wave speed and the internal radial artery diameter the volume flow was calculated by Womersley analysis following truncation of the late diastolic phase.</p> <p>Results</p> <p>No significant difference was found between Fabry patients and controls for internal or external arterial diameters, the incremental Young's modulus, the arterial wall thickness, the pulse wave speed and the basal radial artery blood flow. Further, no significant difference was found for the radial artery blood flow in response to intra-arterial acetylcholine or sodium nitroprusside. Both drugs however, elevated the mean arterial flow.</p> <p>Conclusions</p> <p>The current study suggests that no structural or mechanical abnormality exists in the vessel wall of fibro-muscular arteries in Fabry disease. This may indicate that a functional abnormality downstream to the conductance vessels is the dominant feature in development Fabry vasculopathy.</p> http://www.biomedcentral.com/1471-2261/2/1
collection DOAJ
language English
format Article
sources DOAJ
author Dimitriadis Emilios
Campia Umberto
Panza Julio A
Pursley Randall
Altarescu Gheona
Moore David F
Schiffmann Raphael
spellingShingle Dimitriadis Emilios
Campia Umberto
Panza Julio A
Pursley Randall
Altarescu Gheona
Moore David F
Schiffmann Raphael
Arterial Wall Properties and Womersley Flow in Fabry Disease
BMC Cardiovascular Disorders
author_facet Dimitriadis Emilios
Campia Umberto
Panza Julio A
Pursley Randall
Altarescu Gheona
Moore David F
Schiffmann Raphael
author_sort Dimitriadis Emilios
title Arterial Wall Properties and Womersley Flow in Fabry Disease
title_short Arterial Wall Properties and Womersley Flow in Fabry Disease
title_full Arterial Wall Properties and Womersley Flow in Fabry Disease
title_fullStr Arterial Wall Properties and Womersley Flow in Fabry Disease
title_full_unstemmed Arterial Wall Properties and Womersley Flow in Fabry Disease
title_sort arterial wall properties and womersley flow in fabry disease
publisher BMC
series BMC Cardiovascular Disorders
issn 1471-2261
publishDate 2002-01-01
description <p>Abstract</p> <p>Background</p> <p>Fabry disease is an X-linked recessive lysosomal storage disease resulting in the cellular accumulation of globotriaosylceramide particularly globotriaosylceramide. The disease is characterized by a dilated vasculopathy with arterial ectasia in muscular arteries and arterioles. Previous venous plethysomographic studies suggest enhanced endothelium-dependent vasodilation in Fabry disease indicating a functional abnormality of resistance vessels.</p> <p>Methods</p> <p>We examined the mechanical properties of the radial artery in Fabry disease, a typical fibro-muscular artery. Eight control subjects and seven patients with Fabry disease had a right brachial arterial line placed allowing real time recording of intra-arterial blood pressure. Real time B-mode ultrasound recordings of the right radial artery were obtained simultaneously allowing calculation of the vessel wall internal and external diameter, the incremental Young's modulus and arterial wall thickness. By simultaneously measurement of the distal index finger-pulse oximetry the pulse wave speed was calculated. From the wave speed and the internal radial artery diameter the volume flow was calculated by Womersley analysis following truncation of the late diastolic phase.</p> <p>Results</p> <p>No significant difference was found between Fabry patients and controls for internal or external arterial diameters, the incremental Young's modulus, the arterial wall thickness, the pulse wave speed and the basal radial artery blood flow. Further, no significant difference was found for the radial artery blood flow in response to intra-arterial acetylcholine or sodium nitroprusside. Both drugs however, elevated the mean arterial flow.</p> <p>Conclusions</p> <p>The current study suggests that no structural or mechanical abnormality exists in the vessel wall of fibro-muscular arteries in Fabry disease. This may indicate that a functional abnormality downstream to the conductance vessels is the dominant feature in development Fabry vasculopathy.</p>
url http://www.biomedcentral.com/1471-2261/2/1
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