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Effect of oral glucocorticoid intake on autonomic cardiovascular control

This study analyzed baroreflex sensitivity, heart rate and systolic blood pressure variabilities during an oral 1 week administration of prednisone. This study examined the hypothesis that prednisone might change both systolic blood pressure level and baroreflex sensitivity. Twelve physically active...

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Detalles Bibliográficos
Autores principales: Cottin, F., Malcurat, V., Zorgati, H., Prieur, F., Labsy, Z., Do, M. C., Gagey, O., Collomp, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627994/
https://www.ncbi.nlm.nih.gov/pubmed/26543757
http://dx.doi.org/10.1186/s40064-015-1378-8
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author Cottin, F.
Malcurat, V.
Zorgati, H.
Prieur, F.
Labsy, Z.
Do, M. C.
Gagey, O.
Collomp, K.
author_facet Cottin, F.
Malcurat, V.
Zorgati, H.
Prieur, F.
Labsy, Z.
Do, M. C.
Gagey, O.
Collomp, K.
author_sort Cottin, F.
collection PubMed
description This study analyzed baroreflex sensitivity, heart rate and systolic blood pressure variabilities during an oral 1 week administration of prednisone. This study examined the hypothesis that prednisone might change both systolic blood pressure level and baroreflex sensitivity. Twelve physically active male subjects participated to a double-blind, randomized cross-over study consisting of two 1-week periods of treatment separated by a 4-week drug-free washout period: placebo (PLA) or prednisone (PRED). Trials were performed by each subject four times on the second (D2) and seventh (D7) day of each treatment period. ECG and blood pressure were continuously recorded to compute heart rate variability, systolic blood pressure variability and baroreflex sensitivity components with the smoothed pseudo Wigner Ville distribution and baroreflex analysis. Following D2 prednisone treatment, both HR (PLA: 60.8 ± 10.5 vs. PRED: 65.8 ± 9.1 beats min(−1), p = 0.008) and low frequency component of systolic blood pressure variability (D2: 3.09 ± 0.19 vs. D7: 2.34 ± 0.19, p < 0.041) increased whereas other components did not change. Over 7 days of treatment, LF-SBP amplitude increased (D2: 2.71 ± 0.89 vs. D7: 3.87 ± 0.6 mmHg, p = 0.037). A slight increase in both HR and LF-SBPV were observed suggesting a potential sympathetic cardiovascular stimulus. Although we found a significant effect of the 1-week prednisone treatment on heart rate and low frequency power of systolic blood pressure variability, we reported neither an increase in the systolic blood pressure level nor a decrease in the baroreflex sensitivity. Therefore, the fragility of our results cannot support a deleterious effect of 1-week administration of prednisone on the autonomic cardiovascular control which might be involved in cardiovascular diseases.
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spelling pubmed-46279942015-11-05 Effect of oral glucocorticoid intake on autonomic cardiovascular control Cottin, F. Malcurat, V. Zorgati, H. Prieur, F. Labsy, Z. Do, M. C. Gagey, O. Collomp, K. Springerplus Research This study analyzed baroreflex sensitivity, heart rate and systolic blood pressure variabilities during an oral 1 week administration of prednisone. This study examined the hypothesis that prednisone might change both systolic blood pressure level and baroreflex sensitivity. Twelve physically active male subjects participated to a double-blind, randomized cross-over study consisting of two 1-week periods of treatment separated by a 4-week drug-free washout period: placebo (PLA) or prednisone (PRED). Trials were performed by each subject four times on the second (D2) and seventh (D7) day of each treatment period. ECG and blood pressure were continuously recorded to compute heart rate variability, systolic blood pressure variability and baroreflex sensitivity components with the smoothed pseudo Wigner Ville distribution and baroreflex analysis. Following D2 prednisone treatment, both HR (PLA: 60.8 ± 10.5 vs. PRED: 65.8 ± 9.1 beats min(−1), p = 0.008) and low frequency component of systolic blood pressure variability (D2: 3.09 ± 0.19 vs. D7: 2.34 ± 0.19, p < 0.041) increased whereas other components did not change. Over 7 days of treatment, LF-SBP amplitude increased (D2: 2.71 ± 0.89 vs. D7: 3.87 ± 0.6 mmHg, p = 0.037). A slight increase in both HR and LF-SBPV were observed suggesting a potential sympathetic cardiovascular stimulus. Although we found a significant effect of the 1-week prednisone treatment on heart rate and low frequency power of systolic blood pressure variability, we reported neither an increase in the systolic blood pressure level nor a decrease in the baroreflex sensitivity. Therefore, the fragility of our results cannot support a deleterious effect of 1-week administration of prednisone on the autonomic cardiovascular control which might be involved in cardiovascular diseases. Springer International Publishing 2015-10-19 /pmc/articles/PMC4627994/ /pubmed/26543757 http://dx.doi.org/10.1186/s40064-015-1378-8 Text en © Cottin et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Cottin, F.
Malcurat, V.
Zorgati, H.
Prieur, F.
Labsy, Z.
Do, M. C.
Gagey, O.
Collomp, K.
Effect of oral glucocorticoid intake on autonomic cardiovascular control
title Effect of oral glucocorticoid intake on autonomic cardiovascular control
title_full Effect of oral glucocorticoid intake on autonomic cardiovascular control
title_fullStr Effect of oral glucocorticoid intake on autonomic cardiovascular control
title_full_unstemmed Effect of oral glucocorticoid intake on autonomic cardiovascular control
title_short Effect of oral glucocorticoid intake on autonomic cardiovascular control
title_sort effect of oral glucocorticoid intake on autonomic cardiovascular control
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627994/
https://www.ncbi.nlm.nih.gov/pubmed/26543757
http://dx.doi.org/10.1186/s40064-015-1378-8
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