Evidence map›Paper›PMID 41837511›Full record

ArticleCurrent medical imaging2026

Small Animal

Matthias Lütgens, Tobias Lindner, Cajetan Lang, Praveen Vasudevan, Brigitte Vollmar, Marc-André Weber, Stefan Polei

Abstract read
In one paragraph

Article in Current medical imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Matthias LütgensInstitute of Diagnostic and Interventional Radiology, Pediatric Radiology and Neuroradiology, Rostock University Medical Center, Rostock, Germany.
Tobias LindnerCore Facility Multimodal Small Animal Imaging, Rostock University Medical Center, Rostock, Germany.
Cajetan LangCentre for Sports Cardiology/EAPC, University Hospital rechts der Isar, Munich, Germany.
Praveen VasudevanInstitute for Experimental Surgery, Rostock University Medical Center, Rostock, Germany.
Brigitte VollmarInstitute for Experimental Surgery, Rostock University Medical Center, Rostock, Germany.
Marc-André WeberInstitute of Diagnostic and Interventional Radiology, Pediatric Radiology and Neuroradiology, Rostock University Medical Center, Rostock, Germany.
Stefan PoleiInstitute of Diagnostic and Interventional Radiology, Pediatric Radiology and Neuroradiology, Rostock University Medical Center, Rostock, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTo determine the metabolic composition of mouse myocardium in vivo, the phosphorus (31P) magnetic resonance spectroscopy (MRS) setup was investigated and optimized. MATERIALS AND

methodsAfter assessment of coil properties, typical spectroscopy sequences were evaluated against each other using metabolite phantoms of adenosine triphosphate (ATP) and phosphocreatine (PCr) on a Bruker 7 T small animal scanner, with respect to signal-to-noise ratio (SNR) and spatial selectivity.

resultsThe free induction decay (FID) in combination with outer volume suppression (OVS) showed the best SNR compared to the other spectroscopy sequences. OVS achieved a signal suppression of adjacent metabolites of approximately 84%. The performance of the setup was demonstrated in beating mouse hearts before and after myocardial infarction. A PCr to ATP(γ) ratio change from 2.5 pre-infarction to 1.74 approximately one week post-infarction was observed. DISCUSSION: Among the evaluated methods, FID with OVS provided the best balance between localization accuracy and acquisition efficiency for application in the beating mouse heart. Despite probable signal contamination from surrounding tissue, in vivo measurements revealed post-infarction metabolic changes, evidenced by the reduction in the PCr/ATP(γ) ratio.

conclusionDue to the dynamic nature and small size of the target organ, examination of the beating heart with 31P MRS requires a signal intensity- and noise-optimized implementation. The FID with OVS approach allows clear detection of variations in the ATP to PCr ratio before and after myocardial infarction within an acceptable measurement time (approximately 6.5 min). Image-selected in vivo spectroscopy (ISIS), the only serious competitor to FID with OVS, was found to be less suited for in vivo myocardium investigations due to inherent limitations in signal intensity and SNR.

Indexed as

Adenosine TriphosphateMyocardial InfarctionMyocardiumPhosphocreatineAnimalsMagnetic Resonance SpectroscopyMiceMice, Inbred C57BLPhantoms, ImagingPhosphorus IsotopesSignal-To-Noise RatioAdenosine TriphosphatePhosphocreatinePhosphorus Isotopes31PFree induction decayMRSMyocardiumSmall animalx-nuclei

Identifiers

PMID41837511
PMCPMC13587123

What OpenQuestion holds

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Registered trials

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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.