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Pattern of the Heart Rate Performance Curve in Subjects with Beta-Blocker Treatment and Healthy Controls

(1): Heart rate performance curve (HRPC) in incremental exercise was shown to be not uniform, causing false intensity estimation applying percentages of maximal heart rate (HR(max)). HRPC variations are mediated by β-adrenergic receptor sensitivity. The aim was to study age and sex dependent differe...

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Autores principales: Birnbaumer, Philipp, Traninger, Heimo, Sattler, Matteo C., Borenich, Andrea, Hofmann, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293437/
https://www.ncbi.nlm.nih.gov/pubmed/34287331
http://dx.doi.org/10.3390/jfmk6030061
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author Birnbaumer, Philipp
Traninger, Heimo
Sattler, Matteo C.
Borenich, Andrea
Hofmann, Peter
author_facet Birnbaumer, Philipp
Traninger, Heimo
Sattler, Matteo C.
Borenich, Andrea
Hofmann, Peter
author_sort Birnbaumer, Philipp
collection PubMed
description (1): Heart rate performance curve (HRPC) in incremental exercise was shown to be not uniform, causing false intensity estimation applying percentages of maximal heart rate (HR(max)). HRPC variations are mediated by β-adrenergic receptor sensitivity. The aim was to study age and sex dependent differences in HRPC patterns in adults with β-blocker treatment (BB) and healthy controls (C). (2): A total of 535 (102 female) BB individuals were matched 1:1 for age and sex (male 59 ± 11 yrs, female 61 ± 11 yrs) in C. From the maximum incremental cycle ergometer exercise a first and second heart rate (HR) threshold (Th1 and Th2) was determined. Based on the degree of the deflection (kHR), HRPCs were categorized as regular (downward deflection (kHR > 0.1)) and non-regular (upward deflection (kHR < 0.1), linear time course). (3): Logistic regression analysis revealed a higher odds ratio to present a non-regular curve in BB compared to C (females showed three times higher odds). The odds for non-regular HRPC in BB versus C decreased with older age (OR interaction = 0.97, CI = 0.94–0.99). Maximal and submaximal performance and HR variables were significantly lower in BB (p < 0.05). %HR(max) was significantly lower in BB versus C at Th2 (male: 77.2 ± 7.3% vs. 80.8 ± 5.0%; female: 79.2 ± 5.1% vs. 84.0 ± 4.3%). %P(max) at Th2 was similar in BB and C. (4): The HRPC pattern in incremental cycle ergometer exercise is different in individuals receiving β-blocker treatment compared to healthy individuals. The effects were also dependent on age and sex. Relative HR values at Th2 varied substantially depending on treatment. Thus, the percentage of Pmax seems to be a stable and independent indicator for exercise intensity prescription.
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spelling pubmed-82934372021-07-22 Pattern of the Heart Rate Performance Curve in Subjects with Beta-Blocker Treatment and Healthy Controls Birnbaumer, Philipp Traninger, Heimo Sattler, Matteo C. Borenich, Andrea Hofmann, Peter J Funct Morphol Kinesiol Article (1): Heart rate performance curve (HRPC) in incremental exercise was shown to be not uniform, causing false intensity estimation applying percentages of maximal heart rate (HR(max)). HRPC variations are mediated by β-adrenergic receptor sensitivity. The aim was to study age and sex dependent differences in HRPC patterns in adults with β-blocker treatment (BB) and healthy controls (C). (2): A total of 535 (102 female) BB individuals were matched 1:1 for age and sex (male 59 ± 11 yrs, female 61 ± 11 yrs) in C. From the maximum incremental cycle ergometer exercise a first and second heart rate (HR) threshold (Th1 and Th2) was determined. Based on the degree of the deflection (kHR), HRPCs were categorized as regular (downward deflection (kHR > 0.1)) and non-regular (upward deflection (kHR < 0.1), linear time course). (3): Logistic regression analysis revealed a higher odds ratio to present a non-regular curve in BB compared to C (females showed three times higher odds). The odds for non-regular HRPC in BB versus C decreased with older age (OR interaction = 0.97, CI = 0.94–0.99). Maximal and submaximal performance and HR variables were significantly lower in BB (p < 0.05). %HR(max) was significantly lower in BB versus C at Th2 (male: 77.2 ± 7.3% vs. 80.8 ± 5.0%; female: 79.2 ± 5.1% vs. 84.0 ± 4.3%). %P(max) at Th2 was similar in BB and C. (4): The HRPC pattern in incremental cycle ergometer exercise is different in individuals receiving β-blocker treatment compared to healthy individuals. The effects were also dependent on age and sex. Relative HR values at Th2 varied substantially depending on treatment. Thus, the percentage of Pmax seems to be a stable and independent indicator for exercise intensity prescription. MDPI 2021-07-13 /pmc/articles/PMC8293437/ /pubmed/34287331 http://dx.doi.org/10.3390/jfmk6030061 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Birnbaumer, Philipp
Traninger, Heimo
Sattler, Matteo C.
Borenich, Andrea
Hofmann, Peter
Pattern of the Heart Rate Performance Curve in Subjects with Beta-Blocker Treatment and Healthy Controls
title Pattern of the Heart Rate Performance Curve in Subjects with Beta-Blocker Treatment and Healthy Controls
title_full Pattern of the Heart Rate Performance Curve in Subjects with Beta-Blocker Treatment and Healthy Controls
title_fullStr Pattern of the Heart Rate Performance Curve in Subjects with Beta-Blocker Treatment and Healthy Controls
title_full_unstemmed Pattern of the Heart Rate Performance Curve in Subjects with Beta-Blocker Treatment and Healthy Controls
title_short Pattern of the Heart Rate Performance Curve in Subjects with Beta-Blocker Treatment and Healthy Controls
title_sort pattern of the heart rate performance curve in subjects with beta-blocker treatment and healthy controls
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293437/
https://www.ncbi.nlm.nih.gov/pubmed/34287331
http://dx.doi.org/10.3390/jfmk6030061
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