MR angiography of the head/neck vascular system in mice on a clinical mri system

Carolin Reimann, Julia Brangsch, Lisa Christine Adams, Christa Thöne-Reineke, Bernd Hamm, Marcus Richard Makowski

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Background. Magnetic resonance angiography (MRA) represents a clinical reference standard for the in vivo assessment of the vasculature. In this study, the potential of non-contrast-enhanced and contrast-enhanced angiography of the head/neck vasculature in mice on a clinical MR imaging system was tested. Methods. All in vivo magnetic resonance imaging was performed with a 3T clinical system (Siemens). Non-contrast-enhanced (time-of-flight, TOF) and contrast-enhanced angiography (gadofosveset-Trisodium, GdT) were performed in C57BL/6J mouse strain. Lumen-To-muscle ratios (LMRs) and area measurements were assessed. Histology was performed as reference standard of all relevant vascular structures. Results. A close correlation between TOF (R2 = 0.79; p<0.05) and contrast-enhanced (GdT) angiography (R2 = 0.92; p<0.05) with histological area measurements was found. LMRs were comparable between both sequences. Regarding interobserver reproducibility, contrast-enhanced (GdT) angiography yielded a smaller 95% confidence interval and a closer interreader correlation compared to non-contrast-enhanced (TOF) measurements (-0.73-0.89; R2 = 0.81 vs.-0.55-0.56; R2 = 0.94). Conclusion. This study demonstrates that non-contrast-enhanced and contrast-enhanced angiographies of the head/neck vasculature of small animals can reliably performed on a clinical 3T MR scanner. Contrast-enhanced angiography enables the visualization of vascular structures with higher intravascular contrast and higher reproducibility.

Original languageEnglish
Article number5461809
JournalContrast Media and Molecular Imaging
Volume2019
DOIs
StatePublished - 2019
Externally publishedYes

Fingerprint

Dive into the research topics of 'MR angiography of the head/neck vascular system in mice on a clinical mri system'. Together they form a unique fingerprint.

Cite this