Non-invasive vascular resistance assessment of the main branch of the cerebral venous tree using 3D phase-contrast MR angiography
Sidy Fall1, Gwenael Page2, Jean-Marc Constans3, and Olivier Baledent1,4

1BioFlowImage, University of Picardy Jules Verne, AMIENS, France, 2BioFlowImage, University of Picardy Jules Verne, Amiens, France, 3Radiology Department, University Hospital of Picardy, Amiens, France, 4Image Processing Department, University Hospital of Picardy, Amiens, France

Synopsis

The venous drainage system may be influenced by the blood outflow resistance. Precise quantitative measurements of intracranial venous resistance are few. Phase-contrast (PC) MR angiography was used to quantify vascular resistance (VR) of the global cerebral venous system and to explore the correlations between the estimated resistances and the venous outflows measured by cine phase contrast (PC) MRI. Twenty six healthy volunteers participated in this study. The sum of resistances of the transverse sinus, sigmoid sinus and jugular vein correlated with the blood flows measured at C2C3 level: left R2 =0.39 and right R2 = 0.40 .

PURPOSE

The global intracranial venous resistance is still unknown and hemodynamic abnormalities of the cerebral venous system are commonly recognized to be present in several cerebral diseases (1;2). The intracranial pressure is influenced by the blood outflow resistance. Cross-sectional anatomical information from MR angiography (MRA) techniques are currently used to examine cerebral venous insufficiency. However, such measurements of local vessels caliber does not enable the assessment of the total resistance to blood flow along branch of the cerebral venous tree. In this study we propose a new approach to estimate the vascular resistance (VR) of the cerebral venous tree using phase contrast (PC) MR angiography technique. In addition, we examined the correlations between the estimated resistances and the venous outflows measured by cine phase contrast (PC) MRI.

METHODS

Imaging: This study was IRB approved and informed consent was obtained from a cohort of 26 healthy subjects (age=27±6 years). Imaging was performed on a 32-channel, 3T system (Philips Healthcare, Best, The Netherlands). 3D PCA data were acquired with: FOV = 230x230 mm2, resulting spatial resolution = 0.5x0.5x0.5 mm3, α= 12°, Venc = 30 cm/s, TR/TE = 6/3 ms, scan time= 5.9 mn. The scan parameters for the 2D PC-MRI sequence were: FOV = 120x120 mm2, resulting spatial resolution = 0.5x0.5 mm2, TR/TE = 14/8 ms, α= 30°, Venc = 80 cm/s, cardiac phases = 16, scan time = 2.6 mn. Post-processing: A semi-automatic software (www.tidam.fr) tool was applied to quantify the flows from the PC-MRI images. The 3D PC-MRA data were imported to Mimics (Materialise NV, MI, US A) for manual 3D segmentation of the cerebral venous tree (fig. 1) which was represented by the superior sagittal sinus (SSS), straight sinus (StS), left and right transverse sinuses (TS), sigmoid sinuses (SigS) and internal jugular veins (IJV). The length and mean hydraulic diameter were extracted from the segmented geometry. The VR of each branch was estimated using the laminar Poiseuille's law: $$$R_{branch}={\frac{8{\eta}L}{\pi{r_h^4}}}$$$, where $$$ {\eta} $$$ is the blood viscosity, $$${L}$$$ lenght of segment and $$${ r_{h}}$$$ hydraulic radius of segment. An equivalent resistance of the venous tree was calculated using an electric circuit analog to this venous system (fig. 2).

RESULTS

Table1 presents estimated VR. The mean flows measured at the C2C3 cervical level were 353 ± 136 cm3/mn (left IJV) and 262 ± 110 cm3/mn (right IJV). The sum of resistances of the TS, SigS and IJV correlated with the blood flows measured at C2C3 level: R2 = 0.39 for the left side and R2 = 0.40 for the right side (p<0.05).

DISCUSSION and CONCLUSION

By using PC-MRA this new approach allowed to evaluate the global resistance of the venous tree. The relative variability of VR across the subjects may reflect anatomical variations of the venous sinuses. The correlations between left and right C2C3 blood flow measurements and VR may indicate a high level of consistency between the two techniques and shows great promise to detect longitudinal pressure drop (ΔP) as the product between VR and cerebral venous flow measurements (3). The evaluation of ΔP in the venous system can be promising for understanding venous flow alterations in idiopathic intracranial hypertension (4) and hydrocephalus (1).

Acknowledgements

Grant support by ANR-12-MONU-0010

Institut Faire Faces (imaging).

References

1-Sainte-Rose C. et al. Hydrocephalus of venous origin. Neurochirurgie. 1989;

2-Kwon BJ. et al. MR imaging findings of intracranial dural arteriovenous fistulas: relations with venous drainage patterns. AJNR 2005.

3- Stoquart-Elsankari S et al. A phase-contrast MRI study of physiologic cerebral venous flow. J. Cereb. Blood Flow Metab,2009.

4- Dhungana S, et al. Idiopathic intracranial hypertension. Acta Neurol. Scand. 2010.

Figures

Fig.1: left : 3D PC-MRA map of the venous tree; right: example of segmentation of the venous tree with Mimics.

Fig. 2: Schematic representation of the modeled venous system; R. Resistance.

Table1: Summary of estimated vascular resistances in our study group.



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
2579