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Augmentation index assessed by applanation tonometry is elevated in Marfan Syndrome

BACKGROUND: To examine whether augmentation index (AIx) is increased in Marfan syndrome (MFS) and associated with increased aortic root size, and whether a peripheral-to-central generalised transfer function (GTF) can be applied usefully in MFS. METHODS: 10 MFS patients and 10 healthy controls (matc...

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Autores principales: Payne, Rupert A, Hilling-Smith, Roland C, Webb, David J, Maxwell, Simon R, Denvir, Martin A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2169245/
https://www.ncbi.nlm.nih.gov/pubmed/17956619
http://dx.doi.org/10.1186/1749-8090-2-43
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author Payne, Rupert A
Hilling-Smith, Roland C
Webb, David J
Maxwell, Simon R
Denvir, Martin A
author_facet Payne, Rupert A
Hilling-Smith, Roland C
Webb, David J
Maxwell, Simon R
Denvir, Martin A
author_sort Payne, Rupert A
collection PubMed
description BACKGROUND: To examine whether augmentation index (AIx) is increased in Marfan syndrome (MFS) and associated with increased aortic root size, and whether a peripheral-to-central generalised transfer function (GTF) can be applied usefully in MFS. METHODS: 10 MFS patients and 10 healthy controls (matched for sex, age and height) were studied before and after 400 μg sub-lingual GTN. Arterial waveforms were recorded using applanation tonometry. AIx and pulse pressure (PP) were determined for the radial and carotid arteries. Pulse wave velocity (PWV) was measured between carotid and femoral arteries. GTFs were generated to examine the relationship between radial and carotid waveforms. RESULTS: AIx was greater in MFS compared to controls at radial (mean -31.4 (SD 14.3)% v -50.2(15.6)%, p = 0.003) and carotid (-7.6(11.2)% v -23.7(12.7)%, p = 0.004) sites. Baseline PP at all measurement sites, and PWV, did not differ between subject groups. Multivariate analysis demonstrated that PWV and carotid AIx were positively correlated with aortic root size (p < 0.001 and p = 0.012 respectively), independent of the presence of MFS. PP was not associated with aortic root size. GTN caused similar decreases in AIx in both controls and patients. Significant differences were found in GTFs between MFS and control subjects, which changed following GTN administration. However, when an independent GTF was used to derive carotid waves from radial waves, no differences were found in the degree of error between MFS and controls. CONCLUSION: AIx is sensitive to the vascular abnormalities present in MFS, and may have a role as an adjunct to measurement of central PP and PWV. Differences between MFS and controls in the nature of the peripheral-to-central GTF are present, although have little effect on the pulse contour.
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spelling pubmed-21692452007-12-29 Augmentation index assessed by applanation tonometry is elevated in Marfan Syndrome Payne, Rupert A Hilling-Smith, Roland C Webb, David J Maxwell, Simon R Denvir, Martin A J Cardiothorac Surg Research Article BACKGROUND: To examine whether augmentation index (AIx) is increased in Marfan syndrome (MFS) and associated with increased aortic root size, and whether a peripheral-to-central generalised transfer function (GTF) can be applied usefully in MFS. METHODS: 10 MFS patients and 10 healthy controls (matched for sex, age and height) were studied before and after 400 μg sub-lingual GTN. Arterial waveforms were recorded using applanation tonometry. AIx and pulse pressure (PP) were determined for the radial and carotid arteries. Pulse wave velocity (PWV) was measured between carotid and femoral arteries. GTFs were generated to examine the relationship between radial and carotid waveforms. RESULTS: AIx was greater in MFS compared to controls at radial (mean -31.4 (SD 14.3)% v -50.2(15.6)%, p = 0.003) and carotid (-7.6(11.2)% v -23.7(12.7)%, p = 0.004) sites. Baseline PP at all measurement sites, and PWV, did not differ between subject groups. Multivariate analysis demonstrated that PWV and carotid AIx were positively correlated with aortic root size (p < 0.001 and p = 0.012 respectively), independent of the presence of MFS. PP was not associated with aortic root size. GTN caused similar decreases in AIx in both controls and patients. Significant differences were found in GTFs between MFS and control subjects, which changed following GTN administration. However, when an independent GTF was used to derive carotid waves from radial waves, no differences were found in the degree of error between MFS and controls. CONCLUSION: AIx is sensitive to the vascular abnormalities present in MFS, and may have a role as an adjunct to measurement of central PP and PWV. Differences between MFS and controls in the nature of the peripheral-to-central GTF are present, although have little effect on the pulse contour. BioMed Central 2007-10-23 /pmc/articles/PMC2169245/ /pubmed/17956619 http://dx.doi.org/10.1186/1749-8090-2-43 Text en Copyright © 2007 Payne et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Payne, Rupert A
Hilling-Smith, Roland C
Webb, David J
Maxwell, Simon R
Denvir, Martin A
Augmentation index assessed by applanation tonometry is elevated in Marfan Syndrome
title Augmentation index assessed by applanation tonometry is elevated in Marfan Syndrome
title_full Augmentation index assessed by applanation tonometry is elevated in Marfan Syndrome
title_fullStr Augmentation index assessed by applanation tonometry is elevated in Marfan Syndrome
title_full_unstemmed Augmentation index assessed by applanation tonometry is elevated in Marfan Syndrome
title_short Augmentation index assessed by applanation tonometry is elevated in Marfan Syndrome
title_sort augmentation index assessed by applanation tonometry is elevated in marfan syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2169245/
https://www.ncbi.nlm.nih.gov/pubmed/17956619
http://dx.doi.org/10.1186/1749-8090-2-43
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