IP Library › Granted Patent US 9,619,875
Granted Patent B2
US 9,619,875 · App. 14/694,319 · Granted Apr 11, 2017

Contrast reagent leakage correction in dynamic susceptibility contrast magnetic resonance imaging

Inventors: William Rooney (Lake Oswego, OR); Xin Li (Beaverton, OR)
Assignee: OREGON HEALTH & SCIENCE UNIVERSITY
G06T7/00A61K49/106G06T7/0016G06T2200/04G06T2207/10088G06T2207/10096G06T2207/30016G06T2207/30096G06T2207/30104
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,619,875
App. No.
14/694,319
Granted
Apr 11, 2017
Kind
B2
Abstract

Disclosed are methods and systems for calculating a contrast reagent (CR) extravasation rate constant and generating a contrast reagent leakage corrected relative cerebral blood volume (rCBV) image map of a brain region from dynamic susceptibility contrast (DSC) magnetic resonance imaging (MRI) time-course image data based on pharmacokinetic first principles. In one example approach, a computerized method may include performing a linearization transform of a DSC MRI time-course equation which accounts for an intravascular contribution and an extravasating component, and calculating CR leakage from a slope of a linear portion of the transformed data.

Claims (84)

1. A computerized method for contrast reagent leakage correction of dynamic susceptibility contrast (DSC) magnetic resonance imaging (MRI) time-course image data of a brain region, the method comprising:

from the DSC MRI time-course image data, computing a pixel time-course of an effective transverse relaxation rate constant change (ΔR 2 *(t)) and an estimate of a time-course of an effective transverse relaxation rate constant change for relative blood ( ΔR 2 * (t));

computing a contrast reagent extravasating rate constant (K L ) from a slope of a linear portion of a mapping of ΔR 2 *(t)/ ΔR 2 * (t) versus ∫ 0 t ΔR 2 *(t′)dt′/ΔR 2 *(t);

generating a relative cerebral blood volume (rCBV) image map;

generating a contrast reagent leakage corrected relative cerebral blood volume (rCBV LC ) image map based on the contrast reagent extravasating rate constant (K L ),

wherein the contrast reagent leakage corrected rCBV LC image map is generated using the equation:

rCBV LC =rCBV un +K L ∫ 0 T dt′∫ 0 t′ Δ R 2 * ( t ) dt

where rCBV LC is the leakage-corrected rCBV, rCBV un is uncorrected rCBV, K L is the contrast reagent extravasating rate constant, and ΔR 2 * (t) is the effective transverse relaxation rate constant change for relative blood.

2. The method of claim 1 , wherein the contrast reagent comprises a gadolinium-based contrast reagent.

3. The method of claim 1 , wherein the linear portion of the mapping corresponds to DSC MRI time-course image data acquired following a transient period of contrast reagent first pass.

4. The method of claim 1 , wherein ΔR 2 *(t) is computed based on a baseline signal intensity and an imaging echo time of a pulse sequence used to acquire the DSC MRI data.

5. The method of claim 1 , wherein ΔR 2 * (t) is computed based on a combination of signal changes from non-leaking pixels within the DSC MRI time-course image data.

6. The method of claim 1 , wherein the DSC MRI time-course image data comprises dynamic T 2 *-weighted images of the brain region acquired using a gradient-echo echo planar imaging pulse sequence.

7. The method of claim 1 , wherein ΔR 2 *(t) is computed according to the equation:

Δ

⁢

⁢

R

2

*

⁡

(

t

)

=

-

ln

⁡

(

S

⁡

(

t

)

S

0

)

TE

where S(t) is the DSC MRI pixel image at time t, S 0 is a baseline signal intensity, and TE is an imaging echo time of a pulse sequence used to acquire the DSC MRI data.

8. The method of claim 1 , wherein the linear portion of the mapping corresponds to DSC MRI time-course image data acquired from approximately 40 seconds after injection of the contrast reagent to approximately 70 seconds after injection of the contrast reagent.

9. A method for producing an image of a patient's brain with a magnetic resonance imaging (MRI) system, comprising:

acquiring dynamic susceptibility contrast (DSC) MRI time-course image data for a region of interest of the brain prior to an injection of a contrast reagent to obtain a baseline signal intensity;

acquiring DSC MRI time-course image data for the region of interest following an injection of a contrast reagent into a blood vessel which induces a differential between the susceptibilities of the blood vessel and tissue in the region of interest;

from the DSC MRI time-course image data, calculating a pixel time-course of an effective transverse relaxation rate constant change (ΔR 2 *(t)) based on the baseline signal intensity and an imaging echo time of a pulse sequence used to acquire the DSC MRI data;

calculating an estimate of a time-course of an effective transverse relaxation rate constant change for relative blood ( ΔR 2 * (t)) based on a combination of signal changes from non-leaking pixels within the DSC MRI time-course image data;

calculating a contrast reagent extravasating rate constant (K L ) from a slope of a linear portion of a mapping of ΔR 2 *(t)/ ΔR 2 * (t) versus ∫ 0 t ΔR 2 * (t′)dt′/ ΔR 2 * (t), where the linear portion of the mapping corresponds to DSC MRI time-course image data acquire following a transient period of contrast reagent first pass;

generating an image map of relative cerebral blood volume (rCBV) in the region of interest based on an integration of ΔR 2 *(t) over the DSC MRI time-course image data for each pixel in the region of interest;

generating a corrected rCBV image map to correct the rCBV image map for leakage of the contrast reagent out of the patient's vasculature based on the contrast reagent extravasating rate constant (K L ); and

outputting the corrected rCBV image map to a display device.

10. The method of claim 9 , wherein the contrast reagent comprises a gadolinium-based contrast reagent.

11. The method of claim 9 , wherein acquiring DSC MRI time-course image data for the region of interest comprises acquiring dynamic T 2 *-weighted images of the region of interest using a gradient-echo echo planar imaging pulse sequence.

12. The method of claim 9 , wherein ΔR 2 *(t) is calculated according to the equation:

Δ

⁢

⁢

R

2

*

⁡

(

t

)

=

-

ln

⁡

(

S

⁡

(

t

)

S

0

)

TE

where S(t) is the DSC MRI pixel image at time t, S 0 is the baseline signal intensity, and TE is the imaging echo time.

13. The method of claim 9 , wherein the linear portion of the mapping corresponds to DSC MRI time-course image data acquired from approximately 40 seconds after injection of the contrast reagent to approximately 70 seconds after injection of the contrast reagent.

14. The method of claim 9 , wherein the corrected rCBV image map is generated according to the equation:

rCBV LC =rCBV un +K L ∫ 0 T dt′∫ 0 t′ Δ R 2 * ( t ) dt

where rCBV LC is the leakage corrected rCBV, rCBV un is uncorrected rCBV, K L is the contrast reagent extravasating rate constant, and ΔR 2 * (t) is the effective transverse relaxation rate constant change for relative blood.

15. The method of claim 9 , further comprising motion correcting the DSC MRI time-course image data.

16. The method or claim 9 , further comprising performing a linear regression on the linear portion of the mapping to obtain the contrast reagent extravasating rate constant.

17. The method of claim 9 , further comprising identifying an intravasation period from the mapping in response to a deviation from linearity in the mapping following the transient period of contrast reagent first pass.

Continuity (2)
Provisional Application 61983905 · Apr 24, 2014
Related Publication 20150310598A1 · Oct 29, 2015