Marta Hendler, Arkadiusz Ziółkowski, Tomasz Sozański, Marek Czosnyka, Magdalena Kasprowicz
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Onset time delay (onset TD) was defined as the time offset between onsets of FV and tHb pulses, and time to tHb max (TTM) as a time difference between the FV pulse onset and tHb pulse maximum.τwas calculated as a product of cerebrovascular compliance and resistance. Onset TD and TTM were compared between normocapnia and hypercapnia, and their associations withτwere assessed.<i>Main results.</i>Onset TD was consistently positive (0.075 s,<i>Q</i>1-<i>Q</i>3: 0.065-0.108 s). Onset TD andτwere significantly shorter in hypercapnia (0.075 s vs 0.071 s,<i>p</i>< 0.001; 0.107 s vs 0.099 s,<i>p</i>< 0.001). Changes in onset TD andτbetween normo- and hypercapnia were significantly correlated (<i>R</i><sub>S</sub>= 0.452,<i>p</i>< 0.01). TTM was correlated withτin normocapnia (<i>R</i><sub>S</sub>= 0.364,<i>p</i>= 0.03), hypercapnia (<i>R</i><sub>S</sub>= 0.407,<i>p</i>= 0.01) and in terms of relative changes (<i>R</i><sub>S</sub>= 0.421,<i>p</i>= 0.01).<i>Significance.</i>There is a time delay between cerebral macro- and microcirculation, which becomes shorter as the cerebral vasculature dilates in hypercapnia.</p>","PeriodicalId":20047,"journal":{"name":"Physiological measurement","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Analysis of time delay between non-invasively measured pulse oscillations in cerebral macro- and microcirculation.\",\"authors\":\"Marta Hendler, Arkadiusz Ziółkowski, Tomasz Sozański, Marek Czosnyka, Magdalena Kasprowicz\",\"doi\":\"10.1088/1361-6579/ae008d\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Objective.</i>Integration of cerebral blood macrocirculation and microcirculation form a crucial aspect of global cerebral blood flow. Our study aimed to investigate time delay between pulse oscillations of cerebral blood flow velocity (FV) and total hemoglobin concentration (tHb) acquired via transcranial Doppler ultrasonography and functional near-infrared spectroscopy, respectively. Additionally, we compared time-related characteristics with cerebral arterial time constant (τ).<i>Approach.</i>The study involved monitoring of FV, tHb, arterial blood pressure and end-tidal CO<sub>2</sub>(EtCO<sub>2</sub>) during 5 min of rest (normocapnia) and 5 min of controlled hypercapnia in 36 healthy subjects (age: 24 years,<i>Q</i>1-<i>Q</i>3: 21-27 years, 15 females). Onset time delay (onset TD) was defined as the time offset between onsets of FV and tHb pulses, and time to tHb max (TTM) as a time difference between the FV pulse onset and tHb pulse maximum.τwas calculated as a product of cerebrovascular compliance and resistance. Onset TD and TTM were compared between normocapnia and hypercapnia, and their associations withτwere assessed.<i>Main results.</i>Onset TD was consistently positive (0.075 s,<i>Q</i>1-<i>Q</i>3: 0.065-0.108 s). Onset TD andτwere significantly shorter in hypercapnia (0.075 s vs 0.071 s,<i>p</i>< 0.001; 0.107 s vs 0.099 s,<i>p</i>< 0.001). Changes in onset TD andτbetween normo- and hypercapnia were significantly correlated (<i>R</i><sub>S</sub>= 0.452,<i>p</i>< 0.01). 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引用次数: 0
摘要
目的:脑血液大循环和微循环的整合是脑血流的重要组成部分。本研究旨在探讨经颅多普勒超声(TCD)和功能近红外光谱(fNIRS)分别获得的脑血流速度(FV)和总血红蛋白浓度(tHb)脉冲振荡的时间延迟。此外,我们比较了脑动脉时间常数(τ)的时间相关特征。方法:研究包括监测36名健康受试者(年龄:24岁,Q1-Q3: 21-27岁,15名女性)在5分钟休息(正常碳酸血症)和5分钟可控高碳酸血症期间的FV、tHb、动脉血压(ABP)和潮末二氧化碳(EtCO2)。启动时间延迟(Onset TD)定义为FV脉冲和tHb脉冲启动之间的时间偏移,到达tHb最大值的时间(TTM)定义为FV脉冲启动与tHb脉冲最大值之间的时间差。τ作为脑血管顺应性和阻力的乘积计算。比较正常碳酸血症和高碳酸血症患者的起病TD和TTM,并评估其与τ的相关性。
;主要结果:起病TD始终呈阳性(0.075 s, Q1-Q3: 0.065-0.108 s)。在高碳酸血症(0.075 s vs 0.071 s, pS=0.452, pS=0.364, p=0.03)、高碳酸血症(RS=0.407, p=0.01)和相对变化(RS=0.421, p=0.01)中,起病TD和τ均显著缩短。
;意义:脑大循环和微循环之间存在时间延迟,随着高碳酸血症时脑血管扩张而缩短。
Analysis of time delay between non-invasively measured pulse oscillations in cerebral macro- and microcirculation.
Objective.Integration of cerebral blood macrocirculation and microcirculation form a crucial aspect of global cerebral blood flow. Our study aimed to investigate time delay between pulse oscillations of cerebral blood flow velocity (FV) and total hemoglobin concentration (tHb) acquired via transcranial Doppler ultrasonography and functional near-infrared spectroscopy, respectively. Additionally, we compared time-related characteristics with cerebral arterial time constant (τ).Approach.The study involved monitoring of FV, tHb, arterial blood pressure and end-tidal CO2(EtCO2) during 5 min of rest (normocapnia) and 5 min of controlled hypercapnia in 36 healthy subjects (age: 24 years,Q1-Q3: 21-27 years, 15 females). Onset time delay (onset TD) was defined as the time offset between onsets of FV and tHb pulses, and time to tHb max (TTM) as a time difference between the FV pulse onset and tHb pulse maximum.τwas calculated as a product of cerebrovascular compliance and resistance. Onset TD and TTM were compared between normocapnia and hypercapnia, and their associations withτwere assessed.Main results.Onset TD was consistently positive (0.075 s,Q1-Q3: 0.065-0.108 s). Onset TD andτwere significantly shorter in hypercapnia (0.075 s vs 0.071 s,p< 0.001; 0.107 s vs 0.099 s,p< 0.001). Changes in onset TD andτbetween normo- and hypercapnia were significantly correlated (RS= 0.452,p< 0.01). TTM was correlated withτin normocapnia (RS= 0.364,p= 0.03), hypercapnia (RS= 0.407,p= 0.01) and in terms of relative changes (RS= 0.421,p= 0.01).Significance.There is a time delay between cerebral macro- and microcirculation, which becomes shorter as the cerebral vasculature dilates in hypercapnia.
期刊介绍:
Physiological Measurement publishes papers about the quantitative assessment and visualization of physiological function in clinical research and practice, with an emphasis on the development of new methods of measurement and their validation.
Papers are published on topics including:
applied physiology in illness and health
electrical bioimpedance, optical and acoustic measurement techniques
advanced methods of time series and other data analysis
biomedical and clinical engineering
in-patient and ambulatory monitoring
point-of-care technologies
novel clinical measurements of cardiovascular, neurological, and musculoskeletal systems.
measurements in molecular, cellular and organ physiology and electrophysiology
physiological modeling and simulation
novel biomedical sensors, instruments, devices and systems
measurement standards and guidelines.