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Exercise modulates sympathetic and vascular function in chronic kidney disease

BACKGROUND: Chronic kidney disease (CKD) is characterized by chronic overactivation of the sympathetic nervous system (SNS), which increases the risk of cardiovascular (CV) disease and mortality. SNS overactivity increases CV risk by multiple mechanisms, including vascular stiffness. We tested the h...

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Autores principales: Jeong, Jinhee, Sprick, Justin D., DaCosta, Dana R., Mammino, Kevin, Nocera, Joe R., Park, Jeanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977504/
https://www.ncbi.nlm.nih.gov/pubmed/36810250
http://dx.doi.org/10.1172/jci.insight.164221
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author Jeong, Jinhee
Sprick, Justin D.
DaCosta, Dana R.
Mammino, Kevin
Nocera, Joe R.
Park, Jeanie
author_facet Jeong, Jinhee
Sprick, Justin D.
DaCosta, Dana R.
Mammino, Kevin
Nocera, Joe R.
Park, Jeanie
author_sort Jeong, Jinhee
collection PubMed
description BACKGROUND: Chronic kidney disease (CKD) is characterized by chronic overactivation of the sympathetic nervous system (SNS), which increases the risk of cardiovascular (CV) disease and mortality. SNS overactivity increases CV risk by multiple mechanisms, including vascular stiffness. We tested the hypothesis that aerobic exercise training would reduce resting SNS activity and vascular stiffness in patients with CKD. METHODS: In this randomized controlled trial, sedentary older adults with CKD underwent 12 weeks of exercise (cycling, n = 32) or stretching (an active control group, n = 26). Exercise and stretching interventions were performed 20–45 minutes/session at 3 days/week and were matched for duration. Primary endpoints include resting muscle sympathetic nerve activity (MSNA) via microneurography, arterial stiffness by central pulse wave velocity (PWV), and aortic wave reflection by augmentation index (AIx). RESULTS: There was a significant group × time interaction in MSNA and AIx with no change in the exercise group but with an increase in the stretching group after 12 weeks. The magnitude of change in MSNA was inversely associated with baseline MSNA in the exercise group. There was no change in PWV in either group over the study period. CONCLUSION: Our data demonstrate that 12 weeks of cycling exercise has beneficial neurovascular effects in patients with CKD. Specifically, exercise training safely and effectively ameliorated the increase in MSNA and AIx observed over time in the control group. This sympathoinhibitory effect of exercise training showed greater magnitude in patients with CKD with higher resting MSNA. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02947750. FUNDING: NIH R01HL135183; NIH R61AT10457; NIH NCATS KL2TR002381; and NIH T32 DK00756; NIH F32HL147547; and VA Merit I01CX001065.
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spelling pubmed-99775042023-03-02 Exercise modulates sympathetic and vascular function in chronic kidney disease Jeong, Jinhee Sprick, Justin D. DaCosta, Dana R. Mammino, Kevin Nocera, Joe R. Park, Jeanie JCI Insight Clinical Medicine BACKGROUND: Chronic kidney disease (CKD) is characterized by chronic overactivation of the sympathetic nervous system (SNS), which increases the risk of cardiovascular (CV) disease and mortality. SNS overactivity increases CV risk by multiple mechanisms, including vascular stiffness. We tested the hypothesis that aerobic exercise training would reduce resting SNS activity and vascular stiffness in patients with CKD. METHODS: In this randomized controlled trial, sedentary older adults with CKD underwent 12 weeks of exercise (cycling, n = 32) or stretching (an active control group, n = 26). Exercise and stretching interventions were performed 20–45 minutes/session at 3 days/week and were matched for duration. Primary endpoints include resting muscle sympathetic nerve activity (MSNA) via microneurography, arterial stiffness by central pulse wave velocity (PWV), and aortic wave reflection by augmentation index (AIx). RESULTS: There was a significant group × time interaction in MSNA and AIx with no change in the exercise group but with an increase in the stretching group after 12 weeks. The magnitude of change in MSNA was inversely associated with baseline MSNA in the exercise group. There was no change in PWV in either group over the study period. CONCLUSION: Our data demonstrate that 12 weeks of cycling exercise has beneficial neurovascular effects in patients with CKD. Specifically, exercise training safely and effectively ameliorated the increase in MSNA and AIx observed over time in the control group. This sympathoinhibitory effect of exercise training showed greater magnitude in patients with CKD with higher resting MSNA. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02947750. FUNDING: NIH R01HL135183; NIH R61AT10457; NIH NCATS KL2TR002381; and NIH T32 DK00756; NIH F32HL147547; and VA Merit I01CX001065. American Society for Clinical Investigation 2023-02-22 /pmc/articles/PMC9977504/ /pubmed/36810250 http://dx.doi.org/10.1172/jci.insight.164221 Text en © 2023 Jeong et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Medicine
Jeong, Jinhee
Sprick, Justin D.
DaCosta, Dana R.
Mammino, Kevin
Nocera, Joe R.
Park, Jeanie
Exercise modulates sympathetic and vascular function in chronic kidney disease
title Exercise modulates sympathetic and vascular function in chronic kidney disease
title_full Exercise modulates sympathetic and vascular function in chronic kidney disease
title_fullStr Exercise modulates sympathetic and vascular function in chronic kidney disease
title_full_unstemmed Exercise modulates sympathetic and vascular function in chronic kidney disease
title_short Exercise modulates sympathetic and vascular function in chronic kidney disease
title_sort exercise modulates sympathetic and vascular function in chronic kidney disease
topic Clinical Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977504/
https://www.ncbi.nlm.nih.gov/pubmed/36810250
http://dx.doi.org/10.1172/jci.insight.164221
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