Multispectral optoacoustic tomography for non-invasive disease phenotyping in pediatric spinal muscular atrophy patients

Proximal spinal muscular atrophy (SMA) is a rare progressive, life limiting genetic motor neuron disease. While promising causal therapies are available, meaningful prognostic biomarkers for therapeutic monitoring are missing. We demonstrate handheld Multispectral Optoacoustic Tomography (MSOT) as a...

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Autores principales: Adrian P. Regensburger, Alexandra L. Wagner, Vera Danko, Jörg Jüngert, Anna Federle, Daniel Klett, Stephanie Schuessler, Adrian Buehler, Markus F. Neurath, Andreas Roos, Hanns Lochmüller, Joachim Woelfle, Regina Trollmann, Maximilian J. Waldner, Ferdinand Knieling
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Publicado: Elsevier 2022
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spelling oai:doaj.org-article:c614589ba8734c80966616dca9c329592021-11-20T05:06:00ZMultispectral optoacoustic tomography for non-invasive disease phenotyping in pediatric spinal muscular atrophy patients2213-597910.1016/j.pacs.2021.100315https://doaj.org/article/c614589ba8734c80966616dca9c329592022-03-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2213597921000744https://doaj.org/toc/2213-5979Proximal spinal muscular atrophy (SMA) is a rare progressive, life limiting genetic motor neuron disease. While promising causal therapies are available, meaningful prognostic biomarkers for therapeutic monitoring are missing. We demonstrate handheld Multispectral Optoacoustic Tomography (MSOT) as a novel non-invasive imaging approach to visualize and quantify muscle wasting in pediatric SMA. While MSOT signals were distributed homogeneously in muscles of healthy volunteers (HVs), SMA patients showed moth-eaten optoacoustic signal patterns. Further signal quantification revealed greatest differences between groups at the isosbestic point for hemoglobin (SWL 800 nm). The SWL 800 nm signal intensities further correlated with clinical phenotype tested by standard motor outcome measures. Therefore, handheld MSOT could enable non-invasive assessment of disease burden in SMA patients.Adrian P. RegensburgerAlexandra L. WagnerVera DankoJörg JüngertAnna FederleDaniel KlettStephanie SchuesslerAdrian BuehlerMarkus F. NeurathAndreas RoosHanns LochmüllerJoachim WoelfleRegina TrollmannMaximilian J. WaldnerFerdinand KnielingElsevierarticleOptoacousticsPhotoacousticsMultispectral optoacoustic tomographySpinal muscular atrophiePhysicsQC1-999Acoustics. SoundQC221-246Optics. LightQC350-467ENPhotoacoustics, Vol 25, Iss , Pp 100315- (2022)
institution DOAJ
collection DOAJ
language EN
topic Optoacoustics
Photoacoustics
Multispectral optoacoustic tomography
Spinal muscular atrophie
Physics
QC1-999
Acoustics. Sound
QC221-246
Optics. Light
QC350-467
spellingShingle Optoacoustics
Photoacoustics
Multispectral optoacoustic tomography
Spinal muscular atrophie
Physics
QC1-999
Acoustics. Sound
QC221-246
Optics. Light
QC350-467
Adrian P. Regensburger
Alexandra L. Wagner
Vera Danko
Jörg Jüngert
Anna Federle
Daniel Klett
Stephanie Schuessler
Adrian Buehler
Markus F. Neurath
Andreas Roos
Hanns Lochmüller
Joachim Woelfle
Regina Trollmann
Maximilian J. Waldner
Ferdinand Knieling
Multispectral optoacoustic tomography for non-invasive disease phenotyping in pediatric spinal muscular atrophy patients
description Proximal spinal muscular atrophy (SMA) is a rare progressive, life limiting genetic motor neuron disease. While promising causal therapies are available, meaningful prognostic biomarkers for therapeutic monitoring are missing. We demonstrate handheld Multispectral Optoacoustic Tomography (MSOT) as a novel non-invasive imaging approach to visualize and quantify muscle wasting in pediatric SMA. While MSOT signals were distributed homogeneously in muscles of healthy volunteers (HVs), SMA patients showed moth-eaten optoacoustic signal patterns. Further signal quantification revealed greatest differences between groups at the isosbestic point for hemoglobin (SWL 800 nm). The SWL 800 nm signal intensities further correlated with clinical phenotype tested by standard motor outcome measures. Therefore, handheld MSOT could enable non-invasive assessment of disease burden in SMA patients.
format article
author Adrian P. Regensburger
Alexandra L. Wagner
Vera Danko
Jörg Jüngert
Anna Federle
Daniel Klett
Stephanie Schuessler
Adrian Buehler
Markus F. Neurath
Andreas Roos
Hanns Lochmüller
Joachim Woelfle
Regina Trollmann
Maximilian J. Waldner
Ferdinand Knieling
author_facet Adrian P. Regensburger
Alexandra L. Wagner
Vera Danko
Jörg Jüngert
Anna Federle
Daniel Klett
Stephanie Schuessler
Adrian Buehler
Markus F. Neurath
Andreas Roos
Hanns Lochmüller
Joachim Woelfle
Regina Trollmann
Maximilian J. Waldner
Ferdinand Knieling
author_sort Adrian P. Regensburger
title Multispectral optoacoustic tomography for non-invasive disease phenotyping in pediatric spinal muscular atrophy patients
title_short Multispectral optoacoustic tomography for non-invasive disease phenotyping in pediatric spinal muscular atrophy patients
title_full Multispectral optoacoustic tomography for non-invasive disease phenotyping in pediatric spinal muscular atrophy patients
title_fullStr Multispectral optoacoustic tomography for non-invasive disease phenotyping in pediatric spinal muscular atrophy patients
title_full_unstemmed Multispectral optoacoustic tomography for non-invasive disease phenotyping in pediatric spinal muscular atrophy patients
title_sort multispectral optoacoustic tomography for non-invasive disease phenotyping in pediatric spinal muscular atrophy patients
publisher Elsevier
publishDate 2022
url https://doaj.org/article/c614589ba8734c80966616dca9c32959
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