Increased Aortic Stiffness and Related Factors in Patients With Peripheral Arterial Disease

A number of conditions have been associated with functional changes of large arteries. The aim of this study was to evaluate the factors associated with aortic stiffness in patients with peripheral arterial disease (PAD). The authors studied 86 patients with PAD (ankle‐brachial pressure index [ABPI]...

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Published inThe journal of clinical hypertension (Greenwich, Conn.) Vol. 15; no. 10; pp. 712 - 716
Main Authors Catalano, Mariella, Scandale, Giovanni, Carzaniga, Gianni, Cinquini, Michela, Minola, Marzio, Dimitrov, Gabriel, Carotta, Maria
Format Journal Article
LanguageEnglish
Published United States John Wiley and Sons Inc 01.10.2013
Subjects
Online AccessGet full text
ISSN1524-6175
1751-7176
1751-7176
DOI10.1111/jch.12167

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Abstract A number of conditions have been associated with functional changes of large arteries. The aim of this study was to evaluate the factors associated with aortic stiffness in patients with peripheral arterial disease (PAD). The authors studied 86 patients with PAD (ankle‐brachial pressure index [ABPI] ≤0.9) and 86 controls. Aortic stiffness was determined by pulse wave velocity (aPWV) using applanation tonometry. In PAD patients, aPWV was higher compared with controls (11±3 vs 9.8±1.8; P=.002). In multiple regression analysis, aPWV was independently associated with pulse pressure (β=0.05, P=.01) in the PAD patients and with age in the control group (β=0.08, P=.0005). The results of this study confirm an aPWV increase in patients with PAD and emphasize the association between blood pressure and aPWV. Further studies are necessary to assess whether higher aortic stiffening adds prognostic value to ABPI, which is the most powerful prognostic indicator in PAD.
AbstractList A number of conditions have been associated with functional changes of large arteries. The aim of this study was to evaluate the factors associated with aortic stiffness in patients with peripheral arterial disease (PAD). The authors studied 86 patients with PAD (ankle‐brachial pressure index [ABPI] ≤0.9) and 86 controls. Aortic stiffness was determined by pulse wave velocity (aPWV) using applanation tonometry. In PAD patients, aPWV was higher compared with controls (11±3 vs 9.8±1.8; P=.002). In multiple regression analysis, aPWV was independently associated with pulse pressure (β=0.05, P=.01) in the PAD patients and with age in the control group (β=0.08, P=.0005). The results of this study confirm an aPWV increase in patients with PAD and emphasize the association between blood pressure and aPWV. Further studies are necessary to assess whether higher aortic stiffening adds prognostic value to ABPI, which is the most powerful prognostic indicator in PAD.
A number of conditions have been associated with functional changes of large arteries. The aim of this study was to evaluate the factors associated with aortic stiffness in patients with peripheral arterial disease (PAD). The authors studied 86 patients with PAD (ankle‐brachial pressure index [ABPI] ≤0.9) and 86 controls. Aortic stiffness was determined by pulse wave velocity ( aPWV ) using applanation tonometry. In PAD patients, aPWV was higher compared with controls (11±3 vs 9.8±1.8; P =.002). In multiple regression analysis, aPWV was independently associated with pulse pressure (β=0.05, P =.01) in the PAD patients and with age in the control group (β=0.08, P =.0005). The results of this study confirm an aPWV increase in patients with PAD and emphasize the association between blood pressure and aPWV . Further studies are necessary to assess whether higher aortic stiffening adds prognostic value to ABPI, which is the most powerful prognostic indicator in PAD.
A number of conditions have been associated with functional changes of large arteries. The aim of this study was to evaluate the factors associated with aortic stiffness in patients with peripheral arterial disease (PAD). The authors studied 86 patients with PAD (ankle-brachial pressure index [ABPI] ≤0.9) and 86 controls. Aortic stiffness was determined by pulse wave velocity (aPWV) using applanation tonometry. In PAD patients, aPWV was higher compared with controls (11 ± 3 vs 9.8 ± 1.8; P=.002). In multiple regression analysis, aPWV was independently associated with pulse pressure (β=0.05, P=.01) in the PAD patients and with age in the control group (β=0.08, P=.0005). The results of this study confirm an aPWV increase in patients with PAD and emphasize the association between blood pressure and aPWV. Further studies are necessary to assess whether higher aortic stiffening adds prognostic value to ABPI, which is the most powerful prognostic indicator in PAD.A number of conditions have been associated with functional changes of large arteries. The aim of this study was to evaluate the factors associated with aortic stiffness in patients with peripheral arterial disease (PAD). The authors studied 86 patients with PAD (ankle-brachial pressure index [ABPI] ≤0.9) and 86 controls. Aortic stiffness was determined by pulse wave velocity (aPWV) using applanation tonometry. In PAD patients, aPWV was higher compared with controls (11 ± 3 vs 9.8 ± 1.8; P=.002). In multiple regression analysis, aPWV was independently associated with pulse pressure (β=0.05, P=.01) in the PAD patients and with age in the control group (β=0.08, P=.0005). The results of this study confirm an aPWV increase in patients with PAD and emphasize the association between blood pressure and aPWV. Further studies are necessary to assess whether higher aortic stiffening adds prognostic value to ABPI, which is the most powerful prognostic indicator in PAD.
A number of conditions have been associated with functional changes of large arteries. The aim of this study was to evaluate the factors associated with aortic stiffness in patients with peripheral arterial disease (PAD). The authors studied 86 patients with PAD (ankle-brachial pressure index [ABPI] ≤0.9) and 86 controls. Aortic stiffness was determined by pulse wave velocity (aPWV) using applanation tonometry. In PAD patients, aPWV was higher compared with controls (11 ± 3 vs 9.8 ± 1.8; P=.002). In multiple regression analysis, aPWV was independently associated with pulse pressure (β=0.05, P=.01) in the PAD patients and with age in the control group (β=0.08, P=.0005). The results of this study confirm an aPWV increase in patients with PAD and emphasize the association between blood pressure and aPWV. Further studies are necessary to assess whether higher aortic stiffening adds prognostic value to ABPI, which is the most powerful prognostic indicator in PAD.
Author Minola, Marzio
Carzaniga, Gianni
Dimitrov, Gabriel
Carotta, Maria
Scandale, Giovanni
Catalano, Mariella
Cinquini, Michela
AuthorAffiliation 2 Laboratory for the Development of New Pharmacological Strategies Department of Oncology Mario Negri Institute for Pharmacological Research Milan Italy
1 Research Center on Vascular Diseases and Angiology Unit University of Milan Milan Italy
AuthorAffiliation_xml – name: 2 Laboratory for the Development of New Pharmacological Strategies Department of Oncology Mario Negri Institute for Pharmacological Research Milan Italy
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Notes Mr Carotta and Mrs Carzaniga took part in all of the technical phases of the study as scientificic technicians of the Università degli Studi di Milano, Milan, Italy.
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Snippet A number of conditions have been associated with functional changes of large arteries. The aim of this study was to evaluate the factors associated with aortic...
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SubjectTerms Adult
Aged
Aged, 80 and over
Ankle Brachial Index
Aorta - physiopathology
Blood Pressure - physiology
Case-Control Studies
Female
Heart Rate - physiology
Humans
Male
Middle Aged
Original Paper
Original Papers
Peripheral Arterial Disease - physiopathology
Pulse Wave Analysis
Regression Analysis
Risk Assessment
Vascular Stiffness - physiology
Title Increased Aortic Stiffness and Related Factors in Patients With Peripheral Arterial Disease
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjch.12167
https://www.ncbi.nlm.nih.gov/pubmed/24088278
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https://pubmed.ncbi.nlm.nih.gov/PMC8033817
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