Cody R van Rassel, Oluwatimilehin O Ajayi, Kate M Sales, Christian A Clermont, Markus Rummel, Martin J MacInnis
{"title":"心率变异性的分形相关性是增量和恒速跑步过程中运动强度的标记","authors":"Cody R van Rassel, Oluwatimilehin O Ajayi, Kate M Sales, Christian A Clermont, Markus Rummel, Martin J MacInnis","doi":"10.1101/2023.12.19.23300234","DOIUrl":null,"url":null,"abstract":"The short–term scaling exponent of detrended fluctuation analysis (DFAα1) applied to interbeat intervals may provide a method to identify ventilatory thresholds and indicate systemic perturbation during prolonged exercise. The purposes of this study were to i) confirm whether DFAα1 values of 0.75 and 0.5 coincide with the gas exchange threshold (GET) and respiratory compensation point (RCP), ii) quantify DFAα1 during constant-speed running near the maximal lactate steady state (MLSS), and iii) assess the repeatability of DFAα1 between MLSS trials. Seventeen runners performed an incremental running test, and eleven and ten runners also performed constant–speed running 5% below, at, and 5% above the MLSS, and a repeat trial at MLSS, respectively. GET (bias [LOA]: –3.6 [–9.1 to 1.9] mL/kg/min) and RCP (–3.5 [–14.1 to 7.2] mL/kg/min) were overestimated using DFAα1. DFAα1 responses during 30-min running trials near MLSS were variable (i.e., 0.27 to 1.24), and affected by intensity (p=0.019) and duration (p=0.001). No difference in DFAα1 was detected between MLSS trials (p=0.926). These results question whether DFAα1 values can accurately delineate exercise thresholds, but the dependency of DFAα1 on intensity and duration support its potential use to quantify systemic perturbations imposed by continuous exercise.","PeriodicalId":501122,"journal":{"name":"medRxiv - Sports Medicine","volume":"486 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fractal correlation properties of heart rate variability as a marker of exercise intensity during incremental and constant-speed treadmill running\",\"authors\":\"Cody R van Rassel, Oluwatimilehin O Ajayi, Kate M Sales, Christian A Clermont, Markus Rummel, Martin J MacInnis\",\"doi\":\"10.1101/2023.12.19.23300234\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The short–term scaling exponent of detrended fluctuation analysis (DFAα1) applied to interbeat intervals may provide a method to identify ventilatory thresholds and indicate systemic perturbation during prolonged exercise. The purposes of this study were to i) confirm whether DFAα1 values of 0.75 and 0.5 coincide with the gas exchange threshold (GET) and respiratory compensation point (RCP), ii) quantify DFAα1 during constant-speed running near the maximal lactate steady state (MLSS), and iii) assess the repeatability of DFAα1 between MLSS trials. Seventeen runners performed an incremental running test, and eleven and ten runners also performed constant–speed running 5% below, at, and 5% above the MLSS, and a repeat trial at MLSS, respectively. GET (bias [LOA]: –3.6 [–9.1 to 1.9] mL/kg/min) and RCP (–3.5 [–14.1 to 7.2] mL/kg/min) were overestimated using DFAα1. DFAα1 responses during 30-min running trials near MLSS were variable (i.e., 0.27 to 1.24), and affected by intensity (p=0.019) and duration (p=0.001). No difference in DFAα1 was detected between MLSS trials (p=0.926). These results question whether DFAα1 values can accurately delineate exercise thresholds, but the dependency of DFAα1 on intensity and duration support its potential use to quantify systemic perturbations imposed by continuous exercise.\",\"PeriodicalId\":501122,\"journal\":{\"name\":\"medRxiv - Sports Medicine\",\"volume\":\"486 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"medRxiv - Sports Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2023.12.19.23300234\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv - Sports Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2023.12.19.23300234","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Fractal correlation properties of heart rate variability as a marker of exercise intensity during incremental and constant-speed treadmill running
The short–term scaling exponent of detrended fluctuation analysis (DFAα1) applied to interbeat intervals may provide a method to identify ventilatory thresholds and indicate systemic perturbation during prolonged exercise. The purposes of this study were to i) confirm whether DFAα1 values of 0.75 and 0.5 coincide with the gas exchange threshold (GET) and respiratory compensation point (RCP), ii) quantify DFAα1 during constant-speed running near the maximal lactate steady state (MLSS), and iii) assess the repeatability of DFAα1 between MLSS trials. Seventeen runners performed an incremental running test, and eleven and ten runners also performed constant–speed running 5% below, at, and 5% above the MLSS, and a repeat trial at MLSS, respectively. GET (bias [LOA]: –3.6 [–9.1 to 1.9] mL/kg/min) and RCP (–3.5 [–14.1 to 7.2] mL/kg/min) were overestimated using DFAα1. DFAα1 responses during 30-min running trials near MLSS were variable (i.e., 0.27 to 1.24), and affected by intensity (p=0.019) and duration (p=0.001). No difference in DFAα1 was detected between MLSS trials (p=0.926). These results question whether DFAα1 values can accurately delineate exercise thresholds, but the dependency of DFAα1 on intensity and duration support its potential use to quantify systemic perturbations imposed by continuous exercise.