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Altered vascular function in chronic kidney disease: evidence from passive leg movement

Chronic kidney disease (CKD) is an independent risk factor for the development of cardiovascular disease and is characterized by reduced nitric oxide (NO) bioavailability and vascular dysfunction, typically assessed using brachial artery flow‐mediated dilation (FMD). It has been previously reported...

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Autores principales: Katulka, Elissa K., Hirt, Alexandra E., Kirkman, Danielle L., Edwards, David G., Witman, Melissa A. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478620/
https://www.ncbi.nlm.nih.gov/pubmed/31016878
http://dx.doi.org/10.14814/phy2.14075
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author Katulka, Elissa K.
Hirt, Alexandra E.
Kirkman, Danielle L.
Edwards, David G.
Witman, Melissa A. H.
author_facet Katulka, Elissa K.
Hirt, Alexandra E.
Kirkman, Danielle L.
Edwards, David G.
Witman, Melissa A. H.
author_sort Katulka, Elissa K.
collection PubMed
description Chronic kidney disease (CKD) is an independent risk factor for the development of cardiovascular disease and is characterized by reduced nitric oxide (NO) bioavailability and vascular dysfunction, typically assessed using brachial artery flow‐mediated dilation (FMD). It has been previously reported that passive leg movement (PLM)‐induced hyperemia, an assessment of lower extremity vascular function, is highly dependent on NO, but has not yet been utilized to assess vascular function in patients with CKD. The purpose of this study was to comprehensively assess vascular function in patients with CKD using PLM, in addition to the traditional FMD technique. Assessment of vascular function via PLM and FMD was performed on 12 patients (CKD, 66 ± 3 years) and 16 age‐matched healthy controls (CON, 60 ± 2 years). Blood velocity and artery diameters during PLM and FMD were measured using duplex ultrasound of the femoral and brachial arteries, respectively. Habitual physical activity, assessed by accelerometry, was performed in a subset of each group. CKD patients had reduced peak leg blood flow (LBF) (384 ± 39 vs. 569 ± 77 mL/min, P < 0.05) and change in LBF from baseline to peak (∆peakLBF) (143 ± 22 vs. 249 ± 34 mL/min, P < 0.05) during PLM compared to CON. Additionally, PLM responses were significantly associated with kidney function and physical activity levels. As anticipated, FMD was significantly attenuated in CKD patients (5.2 ± 1.1 vs. 8.8 ± 1.2%, P < 0.05). In conclusion, both upper and lower extremity measures of vascular function indicate impairment in CKD patients when compared to controls. PLM appears to be a novel and feasible approach to assessing lower extremity vascular function in CKD.
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spelling pubmed-64786202019-05-01 Altered vascular function in chronic kidney disease: evidence from passive leg movement Katulka, Elissa K. Hirt, Alexandra E. Kirkman, Danielle L. Edwards, David G. Witman, Melissa A. H. Physiol Rep Original Research Chronic kidney disease (CKD) is an independent risk factor for the development of cardiovascular disease and is characterized by reduced nitric oxide (NO) bioavailability and vascular dysfunction, typically assessed using brachial artery flow‐mediated dilation (FMD). It has been previously reported that passive leg movement (PLM)‐induced hyperemia, an assessment of lower extremity vascular function, is highly dependent on NO, but has not yet been utilized to assess vascular function in patients with CKD. The purpose of this study was to comprehensively assess vascular function in patients with CKD using PLM, in addition to the traditional FMD technique. Assessment of vascular function via PLM and FMD was performed on 12 patients (CKD, 66 ± 3 years) and 16 age‐matched healthy controls (CON, 60 ± 2 years). Blood velocity and artery diameters during PLM and FMD were measured using duplex ultrasound of the femoral and brachial arteries, respectively. Habitual physical activity, assessed by accelerometry, was performed in a subset of each group. CKD patients had reduced peak leg blood flow (LBF) (384 ± 39 vs. 569 ± 77 mL/min, P < 0.05) and change in LBF from baseline to peak (∆peakLBF) (143 ± 22 vs. 249 ± 34 mL/min, P < 0.05) during PLM compared to CON. Additionally, PLM responses were significantly associated with kidney function and physical activity levels. As anticipated, FMD was significantly attenuated in CKD patients (5.2 ± 1.1 vs. 8.8 ± 1.2%, P < 0.05). In conclusion, both upper and lower extremity measures of vascular function indicate impairment in CKD patients when compared to controls. PLM appears to be a novel and feasible approach to assessing lower extremity vascular function in CKD. John Wiley and Sons Inc. 2019-04-23 /pmc/articles/PMC6478620/ /pubmed/31016878 http://dx.doi.org/10.14814/phy2.14075 Text en © 2019 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Katulka, Elissa K.
Hirt, Alexandra E.
Kirkman, Danielle L.
Edwards, David G.
Witman, Melissa A. H.
Altered vascular function in chronic kidney disease: evidence from passive leg movement
title Altered vascular function in chronic kidney disease: evidence from passive leg movement
title_full Altered vascular function in chronic kidney disease: evidence from passive leg movement
title_fullStr Altered vascular function in chronic kidney disease: evidence from passive leg movement
title_full_unstemmed Altered vascular function in chronic kidney disease: evidence from passive leg movement
title_short Altered vascular function in chronic kidney disease: evidence from passive leg movement
title_sort altered vascular function in chronic kidney disease: evidence from passive leg movement
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478620/
https://www.ncbi.nlm.nih.gov/pubmed/31016878
http://dx.doi.org/10.14814/phy2.14075
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