Evidence map›Paper›PMID 35403905›Full record

ReviewRadiologie (Heidelberg, Germany)2022

[Noninvasive functional lung imaging with hyperpolarized xenon : Breakthrough for diagnostics?]

Mariia Anikeeva, Maitreyi Sangal, Oliver Speck, Graham Norquay, Maaz Zuhayra, Ulf Lützen, Josh Peters, Olav Jansen, Jan-Bernd Hövener

Open access · hybridAbstract readReview
In one paragraph

Review in Radiologie (Heidelberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 52% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Detection of the Carcinogen Benzo[Analytical chemistry · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 2 countries.

Mariia AnikeevaSektion Biomedizinische Bildgebung, Molecular Imaging North Competence Center (MOIN CC), Klinik für Radiologie und Neuroradiologie, Universtätsklinikum Schleswig-Holstein, Christian-Albrechts-Universität zu Kiel, Am Botanischen Garten 14, 24118, Kiel, Deutschland. Mariia.Anikeeva@rad.uni-kiel.de.
Maitreyi SangalAbteilung Biomedizinische Magnetresonanz, Otto-von-Guericke-Universität Magdeburg, Magdeburg, Deutschland.
Oliver SpeckAbteilung Biomedizinische Magnetresonanz, Otto-von-Guericke-Universität Magdeburg, Magdeburg, Deutschland.
Graham NorquayPOLARIS, Department of Infection, Immunity & Cardiovascular Disease, University of Sheffield, Sheffield, Großbritannien.
Maaz ZuhayraKlinik für Radiologie und Neuroradiologie, Universitätsklinikum Schleswig-Holstein (UKSH), Kiel, Deutschland.
Ulf LützenKlinik für Radiologie und Neuroradiologie, Universitätsklinikum Schleswig-Holstein (UKSH), Kiel, Deutschland.
Josh PetersSektion Biomedizinische Bildgebung, Molecular Imaging North Competence Center (MOIN CC), Klinik für Radiologie und Neuroradiologie, Universtätsklinikum Schleswig-Holstein, Christian-Albrechts-Universität zu Kiel, Am Botanischen Garten 14, 24118, Kiel, Deutschland.
Olav JansenKlinik für Radiologie und Neuroradiologie, Universitätsklinikum Schleswig-Holstein (UKSH), Kiel, Deutschland.
Jan-Bernd HövenerSektion Biomedizinische Bildgebung, Molecular Imaging North Competence Center (MOIN CC), Klinik für Radiologie und Neuroradiologie, Universtätsklinikum Schleswig-Holstein, Christian-Albrechts-Universität zu Kiel, Am Botanischen Garten 14, 24118, Kiel, Deutschland. jan.hoevener@rad.uni-kiel.de.
University Hospital Schleswig-Holstein · DEOtto-von-Guericke University Magdeburg · DEUniversity of Lübeck · DEKiel University · DEUniversity of Sheffield · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMagnetic resonance imaging (MRI) is a noninvasive technique that provides excellent contrast for soft tissue organs. However, due to the low density of protons and many air-tissue junctions, its application in the lung is limited. Thus, X‑ray-based methods are often used here (with the well-known disadvantages of ionizing radiation).

objectivesIn this review, we discuss pulmonary MRI with hyperpolarized xenon-129 (Xe-MRI). Xe-MRI provides unique valuable insights into lung microstructure and function, including gas exchange with red blood cells-parameters not accessible by any standard clinical methods.

methodsBy magnetic labelling, i.e. hyperpolarization, the signal from xenon-129 is amplified by up to 100,000 times. In this process, electrons from rubidium are first polarized to 100% using laser light and then transferred to xenon by collisions. Then the hyperpolarized gas is brought to the patient in a bag and inhaled shortly before the MRI scan.

resultsUsing special programming (sequences) of the MRI, the ventilation, microstructure, or gas exchange of the lungs, can be displayed in 3D. This allows, for example, quantitative visualization of ventilation defects, alveolar size, tissue gas uptake and gas transfer to the blood.

conclusionsXe-MRI provides unique information about the state of the lung-noninvasively, in vivo and in less than a minute.

Indexed as

LungXenonHumansMagnetic Resonance ImagingRespirationXenonGas transferHyperpolarizationMagnetic resonance imagingPulmonary function testsXenon-129

Identifiers

PMID35403905
PMCPMC8996207
OpenAlexW4223488084

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.