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Assessing the pulmonary vascular responsiveness to oxygen with proton MRI.
Kizhakke Puliyakote, Abhilash S; Tedjasaputra, Vincent; Petersen, Gregory M; Sá, Rui Carlos; Hopkins, Susan R.
Afiliação
  • Kizhakke Puliyakote AS; Pulmonary Imaging Laboratory, UC San Diego Health Sciences, La Jolla, California, United States.
  • Tedjasaputra V; Department of Radiology, University of California, San Diego, La Jolla, California, United States.
  • Petersen GM; Pulmonary Imaging Laboratory, UC San Diego Health Sciences, La Jolla, California, United States.
  • Sá RC; Department of Medicine, University of California, San Diego, La Jolla, California, United States.
  • Hopkins SR; Pulmonary Imaging Laboratory, UC San Diego Health Sciences, La Jolla, California, United States.
J Appl Physiol (1985) ; 136(4): 853-863, 2024 Apr 01.
Article em En | MEDLINE | ID: mdl-38385182
ABSTRACT
Ventilation-perfusion matching occurs passively and is also actively regulated through hypoxic pulmonary vasoconstriction (HPV). The extent of HPV activity in humans, particularly normal subjects, is uncertain. Current evaluation of HPV assesses changes in ventilation-perfusion relationships/pulmonary vascular resistance with hypoxia and is invasive, or unsuitable for patients because of safety concerns. We used a noninvasive imaging-based approach to quantify the pulmonary vascular response to oxygen as a metric of HPV by measuring perfusion changes between breathing 21% and 30%O2 using arterial spin labeling (ASL) MRI. We hypothesized that the differences between 21% and 30%O2 images reflecting HPV release would be 1) significantly greater than the differences without [Formula see text] changes (e.g., 21-21% and 30-30%O2) and 2) negatively associated with ventilation-perfusion mismatch. Perfusion was quantified in the right lung in normoxia (baseline), after 15 min of 30% O2 breathing (hyperoxia) and 15 min normoxic recovery (recovery) in healthy subjects (7 M, 7 F; age = 41.4 ± 19.6 yr). Normalized, smoothed, and registered pairs of perfusion images were subtracted and the mean square difference (MSD) was calculated. Separately, regional alveolar ventilation and perfusion were quantified from specific ventilation, proton density, and ASL imaging; the spatial variance of ventilation-perfusion (σ2V̇a/‡) distributions was calculated. The O2-responsive MSD was reproducible (R2 = 0.94, P < 0.0001) and greater (0.16 ± 0.06, P < 0.0001) than that from subtracted images collected under the same [Formula see text] (baseline = 0.09 ± 0.04, hyperoxia = 0.08 ± 0.04, recovery = 0.08 ± 0.03), which were not different from one another (P = 0.2). The O2-responsive MSD was correlated with σ2V̇a/‡ (R2 = 0.47, P = 0.007). These data suggest that active HPV optimizes ventilation-perfusion matching in normal subjects. This noninvasive approach could be applied to patients with different disease phenotypes to assess HPV and ventilation-perfusion mismatch.NEW & NOTEWORTHY We developed a new proton MRI method to noninvasively quantify the pulmonary vascular response to oxygen. Using a hyperoxic stimulus to release HPV, we quantified the resulting redistribution of perfusion. The differences between normoxic and hyperoxic images were greater than those between images without [Formula see text] changes and negatively correlated with ventilation-perfusion mismatch. This suggests that active HPV optimizes ventilation-perfusion matching in normal subjects. This approach is suitable for assessing patients with different disease phenotypes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperóxia / Infecções por Papillomavirus Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperóxia / Infecções por Papillomavirus Idioma: En Ano de publicação: 2024 Tipo de documento: Article