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dc.contributor.author
Gastl, Mareike
dc.contributor.author
Peereboom, Sophie M.
dc.contributor.author
Gotschy, Alexander
dc.contributor.author
Fuetterer, Maximilian
dc.contributor.author
Deuster, von Deuster, Constantin
dc.contributor.author
Boenner, Florian
dc.contributor.author
Kelm, Malte
dc.contributor.author
Schwotzer, Rahel
dc.contributor.author
Flammer, Andreas J.
dc.contributor.author
Manka, Robert
dc.contributor.author
Kozerke, Sebastian
dc.date.accessioned
2019-02-13T11:49:24Z
dc.date.available
2019-02-08T20:01:37Z
dc.date.available
2019-02-13T11:49:24Z
dc.date.issued
2019
dc.identifier.issn
1097-6647
dc.identifier.issn
1532-429X
dc.identifier.other
10.1186/s12968-019-0519-6
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/323988
dc.identifier.doi
10.3929/ethz-b-000323988
dc.description.abstract
Background Cardiac involvement of amyloidosis leads to left-ventricular (LV) wall thickening with progressive heart failure requiring rehospitalization. Cardiovascular magnetic resonance (CMR) is a valuable tool to non-invasively assess myocardial thickening as well as structural changes. Proton CMR spectroscopy (1H-CMRS) additionally allows assessing metabolites including triglycerides (TG) and total creatine (CR). However, opposing results exist regarding utilization of these metabolites in LV hypertrophy or thickening. Therefore, the aim of this study was to measure metabolic alterations using 1H-CMRS in a group of patients with thickened myocardium caused by cardiac amyloidosis. Methods 1H-CMRS was performed on a 1.5 T system (Achieva, Philips Healthcare, Best, The Netherlands) using a 5-channel receive coil in 11 patients with cardiac amyloidosis (60.5 ± 11.4 years, 8 males) and 11 age- and gender-matched controls (63.2 ± 8.9 years, 8 males). After cardiac morphology and function assessment, proton spectra from the interventricular septum (IVS) were acquired using a double-triggered PRESS sequence. Post-processing was performed using a customized reconstruction pipeline based on ReconFrame (GyroTools LLC, Zurich, Switzerland). Spectra were fitted in jMRUI/AMARES and the ratios of triglyceride-to-water (TG/W) and total creatine-to-water (CR/W) were calculated. Results Besides an increased LV mass and a thickened IVS concomitant to the disease characteristics, patients with cardiac amyloidosis presented with decreased global longitudinal (GLS) and circumferential (GCS) strain. LV ejection fraction was preserved relative to controls (60.0 ± 13.2 vs. 66.1 ± 4.3%, p = 0.17). Myocardial TG/W ratios were significantly decreased compared to controls (0.53 ± 0.23 vs. 0.80 ± 0.26%, p = 0.015). CR/W ratios did not show a difference between both groups, but a higher standard deviation in patients with cardiac amyloidosis was observed. Pearson correlation revealed a negative association between elevated LV mass and TG/W (R = − 0.59, p = 0.004) as well as GCS (R = − 0.48, p = 0.025). Conclusions A decrease in myocardial TG/W can be detected in patients with cardiac amyloidosis alongside impaired cardiac function with an association to the degree of myocardial thickening. Accordingly, 1H-CMRS may provide an additional diagnostic tool to gauge progression of cardiac amyloidosis along with standard imaging sequences.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
BioMed Central
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Cardiac amyloidosis
en_US
dc.subject
Cardiovascular magnetic resonance
en_US
dc.subject
Proton spectroscopy
en_US
dc.subject
Myocardial metabolism
en_US
dc.subject
Left-ventricular thickening
en_US
dc.title
Myocardial triglycerides in cardiac amyloidosis assessed by proton cardiovascular magnetic resonance spectroscopy
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
dc.date.published
2019-01-31
ethz.journal.title
Journal of Cardiovascular Magnetic Resonance
ethz.journal.volume
21
en_US
ethz.journal.issue
1
en_US
ethz.journal.abbreviated
J Cardiovasc Magn Reson
ethz.pages.start
10
en_US
ethz.size
10 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
London
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02140 - Dep. Inf.technologie und Elektrotechnik / Dep. of Inform.Technol. Electrical Eng.::02631 - Institut für Biomedizinische Technik / Institute for Biomedical Engineering::09548 - Kozerke, Sebastian / Kozerke, Sebastian
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02140 - Dep. Inf.technologie und Elektrotechnik / Dep. of Inform.Technol. Electrical Eng.::02631 - Institut für Biomedizinische Technik / Institute for Biomedical Engineering::09548 - Kozerke, Sebastian / Kozerke, Sebastian
ethz.date.deposited
2019-02-08T20:01:37Z
ethz.source
SCOPUS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2019-02-13T11:49:37Z
ethz.rosetta.lastUpdated
2021-02-15T03:37:15Z
ethz.rosetta.versionExported
true
ethz.COinS
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