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Journal of Magnetic Resonance Imaging· 2026Q1

Effects of Single and Multiple Dose Tiotropium/Olodaterol in Chronic Obstructive Pulmonary Disease on Alveolar Gas Exchange Measured by Hyperpolarized 129 Xe MRI

Agilo Luitger Kern, Thomas Kayser, Robin Müller, Andreas Voskrebenzev et al.

Short summary

A single dose of tiotropium/olodaterol (TIO/OLO) increased xenon-129 (129Xe) in red blood cells (RBC-Gas) and septal thickness in COPD patients, while multiple doses further improved gas uptake (M-Gas) and RBC-Gas compared to single-dose treatment.

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Key points

  • Single-dose TIO/OLO increased 129Xe in red blood cells (RBC-Gas) and septal thickness in COPD patients.
  • Multiple-dose (14-day) TIO/OLO treatment significantly increased M-Gas and further improved RBC-Gas compared to single-dose.
  • The study utilized hyperpolarized 129Xe MRI to measure gas uptake and microvascular perfusion.
  • 31 participants with COPD and lung hyperinflation were included in the study.

AI-generated from the title and abstract; the full text is not read.

Abstract

ABSTRACT Background Long‐acting muscarinic antagonists/long‐acting beta adrenoreceptor agonists lead to lung deflation and improved microvascular perfusion in hyperinflated chronic obstructive pulmonary disease (COPD), but with an unclear time course. Purpose To investigate the effect of inhalation of tiotropium/olodaterol (TIO/OLO) on MRI measures of gas uptake and microvascular blood volume after single and multiple doses. Study Type Prospective, randomized, investigator‐blinded, placebo‐controlled single‐dose crossover study with open‐label multiple‐dose extension. Population 31 participants with COPD and lung hyperinflation (residual volume > 135% predicted, ≥ 10 pack‐years smoking). Fieldstrength/Sequence 1.5 T/Interleaved 3D radial gas and dissolved‐phase MRI using multi‐echo FLASH, high‐resolution spectroscopy, chemical shift saturation recovery spectroscopy. Assessment Ratios of 129 Xe in membrane tissues (M) to gas (M‐Gas), red blood cells (RBC) to gas (RBC‐Gas), RBC to M (RBC‐M) were calculated from dissolved‐phase imaging. Dissolved‐phase apparent transverse relaxation times (T 2 *) from high‐resolution spectra were also calculated, and septal wall thickness and surface‐volume ratio (S/V) were assessed by fitting a model of xenon exchange functions. Parameters were compared for single‐dose (5 μg/5 μg TIO/OLO) versus placebo using saline, and single‐dose versus multiple‐dose (daily 5 μg/5 μg TIO/OLO for 14 days) treatments. Statistical Tests Linear mixed models with contrasts of estimated marginal means, significance level 0.05. Results Compared with placebo, single‐dose treatment significantly increased RBC‐Gas and septal thickness but not RBC‐M ( p = 0.06), M‐Gas ( p = 0.16), RBC T 2 * ( p = 0.13), M T 2 * ( p = 0.09) and S/V ( p = 0.47). Multiple‐dose treatment significantly increased RBC‐Gas, M‐Gas and M T 2 * compared with single‐dose treatment, but not RBC‐M ( p = 0.82), RBC T 2 * ( p = 0.48), septal thickness ( p = 0.61), and S/V ( p = 0.49). Data Conclusion Single‐dose TIO/OLO increased 129 Xe in RBC‐Gas. Multiple‐dose treatment increased M‐Gas and further increased RBC‐Gas compared to single‐dose treatment. Technical Efficacy Stage 4. Evidence Level 2.

The authors' abstract, as published at the source. Journal of Magnetic Resonance Imaging, 2026 · DOI ↗

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Field: Atomic and Molecular Physics, and Optics

Atomic and Molecular Physics, and OpticsPhysics and Astronomy