Automatic differentiation of placental perfusion compartments by time-to-peak analysis in mice.

INTRODUCTION The aim of this study was to develop an automatic differentiation of two perfusion compartments within the mouse placenta based on times of maximal contrast enhancement for a detailed and reproducible perfusion assessment. METHODS Placentas (n = 17) from pregnant BALB/c mice (n = 10) were examined in vivo at 7T on gestation day 16.5. Coronal dual-echo 3D T1-weighted gradient-echo sequences were acquired after application of contrast agent for dynamic MRI. An adapted gamma variate function was fitted to the discrete concentration time curves to evaluate the effect of noise on perfusion and segmentation results. Time-to-peak maps based on fitted and discrete curves of each placenta were used to classify each voxel into the high- or low-blood flow compartment using k-means clustering. Perfusion analysis was performed using the steepest slope model and also applied to fitted and discrete curves. Results were compared to manually defined compartments from two independent observers using the Dice coefficient D. RESULTS Manually defined placental areas of high-flow and low-flow were similar to the automatic segmentation for discrete (D = 0.76/0.75; D = 0.76/0.79) and fitted (D = 0.80/0.80; D = 0.81/0.82) concentration time curves. Mean perfusion values of discrete and fitted curves ranged in the high-flow compartment from 134 to 142 ml/min/100 ml (discrete) vs. 138-143 ml/min/100 ml (fitted) and in the low-flow compartment from 91 to 94 ml/min/100 ml (discrete) vs. 74-82 ml/min/100 ml (fitted). DISCUSSION Our novel approach allows the automatic differentiation of perfusion compartments of the mouse placenta. The approach may overcome limitations of placental perfusion analyses caused by tissue heterogeneity and a potentially biased selection of regions of interest.

[1]  B S Worthington,et al.  In utero perfusing fraction maps in normal and growth restricted pregnancy measured using IVIM echo-planar MRI. , 2000, Placenta.

[2]  A. Luciani,et al.  Placental perfusion MR imaging with contrast agents in a mouse model. , 2005, Radiology.

[3]  Glyn Johnson,et al.  Dynamic susceptibility contrast perfusion MR imaging of multiple sclerosis lesions: characterizing hemodynamic impairment and inflammatory activity. , 2005, AJNR. American journal of neuroradiology.

[4]  D. Feinberg,et al.  Single‐shot 3D imaging techniques improve arterial spin labeling perfusion measurements , 2005, Magnetic resonance in medicine.

[5]  Fabian Kiessling,et al.  Estimation of tissue perfusion by dynamic contrast-enhanced imaging: simulation-based evaluation of the steepest slope method , 2010, European Radiology.

[6]  Dietmar P. F. Möller,et al.  Fully Automatic Skull-Stripping in 3D Time-of-Flight MRA Image Sequences , 2008, VCBM.

[7]  C. Starmer,et al.  Indicator Transit Time Considered as a Gamma Variate , 1964, Circulation research.

[8]  S. Francis,et al.  In vivo perfusion measurements in the human placenta using echo planar imaging at 0.5 T , 1998, Magnetic resonance in medicine.

[9]  Nils Daniel Forkert,et al.  Reference‐based linear curve fitting for bolus arrival time estimation in 4D MRA and MR perfusion‐weighted image sequences , 2011, Magnetic resonance in medicine.

[10]  Glyn Johnson,et al.  Measuring blood volume and vascular transfer constant from dynamic, T  2* ‐weighted contrast‐enhanced MRI , 2004, Magnetic resonance in medicine.

[11]  Chieko Azuma,et al.  Multispectral quantification of tissue types in a RIF‐1 tumor model with histological validation. Part I , 2007, Magnetic resonance in medicine.

[12]  J. Cross,et al.  Interactions between trophoblast cells and the maternal and fetal circulation in the mouse placenta. , 2002, Developmental biology.

[13]  C. Cuénod,et al.  Measurement of Placental Perfusion by Dynamic Contrast-Enhanced MRI at 4.7 T , 2013, Investigative radiology.

[14]  N. van Bruggen,et al.  Quantification of tumor tissue populations by multispectral analysis , 2004, Magnetic resonance in medicine.

[15]  W. Giles,et al.  Uteroplacental blood flow velocity‐time waveforms in normal and complicated pregnancy , 1985, British journal of obstetrics and gynaecology.

[16]  Richard O. Duda,et al.  Pattern classification and scene analysis , 1974, A Wiley-Interscience publication.

[17]  Y. Ville,et al.  Placental perfusion and permeability: simultaneous assessment with dual-echo contrast-enhanced MR imaging in mice. , 2006, Radiology.

[18]  Vasileios Hatzivassiloglou,et al.  Translating Collocations for Bilingual Lexicons: A Statistical Approach , 1996, CL.

[19]  A. Ferguson-Smith,et al.  Comparative developmental anatomy of the murine and human definitive placentae. , 2002, Placenta.

[20]  In vivo dynamic MRI measurement of the noradrenaline-induced reduction in placental blood flow in mice. , 2006 .

[21]  Anke Meyer-Bäse,et al.  Cluster analysis of dynamic cerebral contrast-enhanced perfusion MRI time-series , 2006, IEEE Transactions on Medical Imaging.

[22]  Daniel Balvay,et al.  Use of Intravoxel Incoherent Motion MR Imaging to Assess Placental Perfusion in a Murine Model of Placental Insufficiency , 2013, Investigative radiology.

[23]  G. Adam,et al.  Application of the steepest slope model reveals different perfusion territories within the mouse placenta. , 2013, Placenta.

[24]  S Rees,et al.  Measurement of tissue perfusion by dynamic computed tomography. , 1992, The British journal of radiology.

[25]  T. Waldhör,et al.  First trimester placental and myometrial blood perfusion measured by 3D power Doppler in normal and unfavourable outcome pregnancies. , 2010, Placenta.

[26]  M. Neeman,et al.  Unique in utero identification of fetuses in multifetal mouse pregnancies by placental bidirectional arterial spin labeling MRI , 2012, Magnetic resonance in medicine.