Anna Costelle, Junlan Lu, Suphachart Leewiwatwong, Berend Westerhof, David Mummy, Sudarshan Rajagopal, Bastiaan Driehuys
{"title":"Combining hyperpolarized <sup>129</sup>Xe MR imaging and spectroscopy to noninvasively estimate pulmonary vascular resistance.","authors":"Anna Costelle, Junlan Lu, Suphachart Leewiwatwong, Berend Westerhof, David Mummy, Sudarshan Rajagopal, Bastiaan Driehuys","doi":"10.1152/japplphysiol.00440.2024","DOIUrl":null,"url":null,"abstract":"<p><p>Hyperpolarized <sup>129</sup>Xe MRI/MRS enables quantitative mapping of function in lung airspaces, membrane tissue, and red blood cells (RBCs) within the pulmonary capillaries. The RBC signal also exhibits cardiogenic oscillations that are reduced in precapillary pulmonary hypertension (PH). This effect is obscured in patients with concomitant defects in transfer from airspaces to RBCs, which increase RBC oscillation amplitudes. Here, we provide a framework for interpreting RBC oscillations and show their relationship to pulsatile blood flow, capillary blood volume, capillary compliance, and impedance of the capillary and venous circulation. This framework was first applied to characterize RBC oscillations in a cohort of subjects with pulmonary disease but no known PH (<i>n</i> = 129). <sup>129</sup>Xe MRI of RBC transfer was used to estimate capillary blood volume, and as it decreased, RBC oscillations sharply increased ([Formula: see text] = 0.53), consistent with model predictions. Model-derived fit parameters were then used to estimate the distribution of pulmonary vascular resistance (PVR) across arterial, capillary, and venous circulation and to correct oscillations for RBC transfer defects. Seventy percent of PVR was estimated to arise from pulmonary arteries, 11% from capillaries, and 19% from veins. When tested in a second cohort of subjects who underwent <sup>129</sup>Xe MRI/MRS and right heart catheterization (<i>n</i> = 40), oscillations corrected for capillary blood volume correlated moderately with PVR (<i>r</i><sup>2</sup> = 0.27, <i>P</i> = 0.0014). For every 1.96 Wood units (WU) increase in PVR, corrected oscillations decreased by 1 absolute percentage point. This work demonstrates that, although <sup>129</sup>Xe-RBC oscillations are only indirectly sensitive to precapillary obstruction, corrected oscillations below 7.5% were 100% specific for elevated PVR.<b>NEW & NOTEWORTHY</b> Cardiogenic oscillations in the <sup>129</sup>Xe red blood cell (RBC) resonance decrease in precapillary pulmonary hypertension (PH) but are enhanced when capillary blood volume is reduced. To separate these effects, we developed a physiological model that used <sup>129</sup>Xe gas exchange MRI to estimate blood volume, which was used to correct oscillation amplitude measurements. Corrected amplitudes correlated significantly with pulmonary vascular resistance, highlighting the potential for future noninvasive detection of PH.</p>","PeriodicalId":15160,"journal":{"name":"Journal of applied physiology","volume":" ","pages":"623-633"},"PeriodicalIF":3.3000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of applied physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/japplphysiol.00440.2024","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/28 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Hyperpolarized 129Xe MRI/MRS enables quantitative mapping of function in lung airspaces, membrane tissue, and red blood cells (RBCs) within the pulmonary capillaries. The RBC signal also exhibits cardiogenic oscillations that are reduced in precapillary pulmonary hypertension (PH). This effect is obscured in patients with concomitant defects in transfer from airspaces to RBCs, which increase RBC oscillation amplitudes. Here, we provide a framework for interpreting RBC oscillations and show their relationship to pulsatile blood flow, capillary blood volume, capillary compliance, and impedance of the capillary and venous circulation. This framework was first applied to characterize RBC oscillations in a cohort of subjects with pulmonary disease but no known PH (n = 129). 129Xe MRI of RBC transfer was used to estimate capillary blood volume, and as it decreased, RBC oscillations sharply increased ([Formula: see text] = 0.53), consistent with model predictions. Model-derived fit parameters were then used to estimate the distribution of pulmonary vascular resistance (PVR) across arterial, capillary, and venous circulation and to correct oscillations for RBC transfer defects. Seventy percent of PVR was estimated to arise from pulmonary arteries, 11% from capillaries, and 19% from veins. When tested in a second cohort of subjects who underwent 129Xe MRI/MRS and right heart catheterization (n = 40), oscillations corrected for capillary blood volume correlated moderately with PVR (r2 = 0.27, P = 0.0014). For every 1.96 Wood units (WU) increase in PVR, corrected oscillations decreased by 1 absolute percentage point. This work demonstrates that, although 129Xe-RBC oscillations are only indirectly sensitive to precapillary obstruction, corrected oscillations below 7.5% were 100% specific for elevated PVR.NEW & NOTEWORTHY Cardiogenic oscillations in the 129Xe red blood cell (RBC) resonance decrease in precapillary pulmonary hypertension (PH) but are enhanced when capillary blood volume is reduced. To separate these effects, we developed a physiological model that used 129Xe gas exchange MRI to estimate blood volume, which was used to correct oscillation amplitude measurements. Corrected amplitudes correlated significantly with pulmonary vascular resistance, highlighting the potential for future noninvasive detection of PH.
期刊介绍:
The Journal of Applied Physiology publishes the highest quality original research and reviews that examine novel adaptive and integrative physiological mechanisms in humans and animals that advance the field. The journal encourages the submission of manuscripts that examine the acute and adaptive responses of various organs, tissues, cells and/or molecular pathways to environmental, physiological and/or pathophysiological stressors. As an applied physiology journal, topics of interest are not limited to a particular organ system. The journal, therefore, considers a wide array of integrative and translational research topics examining the mechanisms involved in disease processes and mitigation strategies, as well as the promotion of health and well-being throughout the lifespan. Priority is given to manuscripts that provide mechanistic insight deemed to exert an impact on the field.