Early detection of lung inflammation: Exploiting T1-effects of iron oxide particles using UTE MRI

被引:29
作者
Strobel, Klaus [1 ]
Hoerr, Verena [1 ]
Schmid, Florian [1 ]
Wachsmuth, Lydia [1 ]
Loeffler, Bettina [2 ]
Faber, Cornelius [1 ]
机构
[1] Univ Hosp Muenster, Dept Clin Radiol, D-48149 Munster, Germany
[2] Univ Hosp Muenster, Inst Med Microbiol, D-48149 Munster, Germany
关键词
ultra-short echo time (UTE); positive contrast; mouse lung; contrast mechanism; Staphylococcus aureus; bacterial infection; IN-VIVO MRI; MAGNETIC-RESONANCE; POSITIVE-CONTRAST; PULMONARY INFLAMMATION; ECHO ACQUISITION; CELLS; NANOPARTICLES; VISUALIZATION; RELAXATION; PARENCHYMA;
D O I
10.1002/mrm.24180
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
At high magnetic fields diagnostic proton MRI of the lung is problematic, because of fast T2* relaxation. The application of superparamagnetic contrast agents and the exploitation of the corresponding T2* effect is inefficient with conventional MRI methods, which limits the early detection of lung diseases. However, a simple theoretical treatment shows that in the lung, by the use of ultra-short echo time sequences, T2* effects can be neglected while T1 shortening effects can be used for signal detection. In our study, we have applied a theoretically and experimentally optimized 3D ultra-short echo time sequence to lung phantoms and to a mouse model of lung inflammation, which was induced by systemic bacterial infection. Following the systemic application of very small superparamagnetic iron oxide nanoparticles, a significant signal increase in the lung of infected animals was detected already at 24 h postinfection, compared to control mice (17%, P < 0.001). Iron accumulation in the lung parenchyma as consequence of the host immune response was histologically confirmed. By conventional T2*- and T2-weighted imaging, neither structural changes nor formation of substantial edema were observed. Magn Reson Med, 2012. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:1924 / 1931
页数:8
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