Ronney B Panerai, Aaron Davies, Abdulaziz Alshehri, Lucy C Beishon, Jatinder S Minhas
{"title":"动态脑自动调节方向敏感性的子成分分析。","authors":"Ronney B Panerai, Aaron Davies, Abdulaziz Alshehri, Lucy C Beishon, Jatinder S Minhas","doi":"10.1152/ajpheart.00498.2024","DOIUrl":null,"url":null,"abstract":"<p><p>The origin of the directional sensitivity (DS) of dynamic cerebral autoregulation (dCA) is not known. In 140 healthy participants (67 male, 27.5 ± 6.1 years old), middle cerebral artery velocity (MCAv, transcranial Doppler), arterial blood pressure (ABP, Finometer), and end-tidal CO2 (EtCO<sub>2</sub>, capnography) were recorded at rest. Critical closing pressure (CrCP) and resistance-area product (RAP) were obtained for each cardiac cycle, as well as mean MCAv and ABP (MAP). The integrated positive and negative derivatives of MAP (MAP<sub>D</sub>, MAP<sub>-D</sub>) were used as simultaneous inputs to an autoregressive moving average model to generate two distinct MCAv step responses. Similar models allowed estimation of corresponding MAP-CrCP and MAP-RAP responses to step changes in MAP<sub>D</sub> and MAP<sub>-D</sub>. The strength of directional sensitivity (ΔDS) was expressed by the difference in mean values of the step responses for the time interval 12-18 s. ΔDS was significant for MCAv (8.5 ± 46.9% vs 26.7 ± 42.0%, p<0.001) and RAP (-93.9 ± 48.1 vs -74.5 ± 43.0%, p<0.001), respectively for MAP<sub>D</sub> and MAP<sub>-D</sub> inputs, but not for CrCP (2.2 ± 48.1% vs 0.72 ± 42.9%, p=0.76). Compared to males, female participants had higher MCAv (63.9 ± 15.6 cm/s vs 55.4 ± 12.9 cm/s, p<0.001), but lower EtCO<sub>2</sub> (p<0.001) and RAP (p=0.015). Sex did not influence ΔDS for any of the three step responses. The presence of directional sensitivity in the RAP, but not in the CrCP transfer function, suggests the origin could be solely myogenic, without metabolic involvement.</p>","PeriodicalId":7692,"journal":{"name":"American journal of physiology. Heart and circulatory physiology","volume":" ","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sub-component analysis of the directional sensitivity of dynamic cerebral autoregulation.\",\"authors\":\"Ronney B Panerai, Aaron Davies, Abdulaziz Alshehri, Lucy C Beishon, Jatinder S Minhas\",\"doi\":\"10.1152/ajpheart.00498.2024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The origin of the directional sensitivity (DS) of dynamic cerebral autoregulation (dCA) is not known. In 140 healthy participants (67 male, 27.5 ± 6.1 years old), middle cerebral artery velocity (MCAv, transcranial Doppler), arterial blood pressure (ABP, Finometer), and end-tidal CO2 (EtCO<sub>2</sub>, capnography) were recorded at rest. Critical closing pressure (CrCP) and resistance-area product (RAP) were obtained for each cardiac cycle, as well as mean MCAv and ABP (MAP). The integrated positive and negative derivatives of MAP (MAP<sub>D</sub>, MAP<sub>-D</sub>) were used as simultaneous inputs to an autoregressive moving average model to generate two distinct MCAv step responses. Similar models allowed estimation of corresponding MAP-CrCP and MAP-RAP responses to step changes in MAP<sub>D</sub> and MAP<sub>-D</sub>. The strength of directional sensitivity (ΔDS) was expressed by the difference in mean values of the step responses for the time interval 12-18 s. ΔDS was significant for MCAv (8.5 ± 46.9% vs 26.7 ± 42.0%, p<0.001) and RAP (-93.9 ± 48.1 vs -74.5 ± 43.0%, p<0.001), respectively for MAP<sub>D</sub> and MAP<sub>-D</sub> inputs, but not for CrCP (2.2 ± 48.1% vs 0.72 ± 42.9%, p=0.76). Compared to males, female participants had higher MCAv (63.9 ± 15.6 cm/s vs 55.4 ± 12.9 cm/s, p<0.001), but lower EtCO<sub>2</sub> (p<0.001) and RAP (p=0.015). Sex did not influence ΔDS for any of the three step responses. The presence of directional sensitivity in the RAP, but not in the CrCP transfer function, suggests the origin could be solely myogenic, without metabolic involvement.</p>\",\"PeriodicalId\":7692,\"journal\":{\"name\":\"American journal of physiology. Heart and circulatory physiology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2024-11-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American journal of physiology. 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Sub-component analysis of the directional sensitivity of dynamic cerebral autoregulation.
The origin of the directional sensitivity (DS) of dynamic cerebral autoregulation (dCA) is not known. In 140 healthy participants (67 male, 27.5 ± 6.1 years old), middle cerebral artery velocity (MCAv, transcranial Doppler), arterial blood pressure (ABP, Finometer), and end-tidal CO2 (EtCO2, capnography) were recorded at rest. Critical closing pressure (CrCP) and resistance-area product (RAP) were obtained for each cardiac cycle, as well as mean MCAv and ABP (MAP). The integrated positive and negative derivatives of MAP (MAPD, MAP-D) were used as simultaneous inputs to an autoregressive moving average model to generate two distinct MCAv step responses. Similar models allowed estimation of corresponding MAP-CrCP and MAP-RAP responses to step changes in MAPD and MAP-D. The strength of directional sensitivity (ΔDS) was expressed by the difference in mean values of the step responses for the time interval 12-18 s. ΔDS was significant for MCAv (8.5 ± 46.9% vs 26.7 ± 42.0%, p<0.001) and RAP (-93.9 ± 48.1 vs -74.5 ± 43.0%, p<0.001), respectively for MAPD and MAP-D inputs, but not for CrCP (2.2 ± 48.1% vs 0.72 ± 42.9%, p=0.76). Compared to males, female participants had higher MCAv (63.9 ± 15.6 cm/s vs 55.4 ± 12.9 cm/s, p<0.001), but lower EtCO2 (p<0.001) and RAP (p=0.015). Sex did not influence ΔDS for any of the three step responses. The presence of directional sensitivity in the RAP, but not in the CrCP transfer function, suggests the origin could be solely myogenic, without metabolic involvement.
期刊介绍:
The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.