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OtherBRAIN

MR Regional Perfusion Imaging: Visualizing Functional Collateral Circulation

C.C.T. Lim, E.T. Petersen, I. Ng, P.Y.K. Hwang, F. Hui and X. Golay
American Journal of Neuroradiology March 2007, 28 (3) 447-448;
C.C.T. Lim
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E.T. Petersen
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I. Ng
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P.Y.K. Hwang
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F. Hui
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X. Golay
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Abstract

SUMMARY: We applied regional perfusion imaging (RPI), a new arterial spin-labeling MR imaging method that selectively studies regions of the brain perfused by individual carotid and basilar arteries. In a patient with cerebrovascular disease, RPI showed cerebral tissue perfused by pial collateral vessels, thereby demonstrating the relationship between anatomic and functional information, which was lacking in conventional x-ray angiography. RPI may be useful to study functional collateral circulation and hence guide therapy in ischemic disease.

Although the collateral circulation is an important determinant of clinical outcome in patients with cerebrovascular occlusion, current methods of evaluation are limited.1–4 We report regional perfusion imaging (RPI), a noninvasive arterial spin-labeling (ASL) MR imaging method that can visualize collateral brain tissue perfusion.

Case Report

A 50-year-old man with no significant history had slurred speech and left-sided weakness. Five days after onset, he underwent combined MR imaging examination in a 3T clinical scanner (Intera; Philips Medical Systems, Best, the Netherlands) with an 8-element parallel imaging-compatible phased-array head coil as part of an institutional review board–approved study. Diffusion-weighted MR imaging (DWI) showed acute infarction of the right corona radiata (Fig 1A), and MR angiography (MRA) revealed right middle cerebral artery (MCA) occlusion (Fig 1B). On the basis of the MRA, RPI was performed by placing selective labeling slabs for ASL over the left internal carotid artery (ICA) (green box, Fig 1B), right ICA, and basilar arteries in turn, by using a single-shot echo-planar imaging sequence (TR/TI/TE = 4000/1500/9.2 ms; spin-echo acquisition and sensitivity encoding factor = 3; matrix = 64 × 64; 60 dynamics; 9 sections; section thickness = 6 mm; scanning time = 3 perfusion territories × 4 minutes = 12 minutes).5 The 3 RPI territories were combined into 1 image for evaluation, with the left ICA colored green; the right ICA, red; and posterior circulation colored blue (Fig 1C). The ischemic right MCA territory received perfusion from the right anterior cerebral artery (in red) and from posterior circulation collaterals (in blue). X-ray angiography confirmed the pial collateral supply (Fig 1D). The area not supplied by any vascular territory (arrows in C) corresponded to a region of decreased vascular reserve on acetazolamide challenge single-photon emission CT (SPECT) (Fig 1E). The patient was treated with aspirin and underwent successful right external carotid-to-internal carotid artery bypass and recovered with full motor power.

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Fig 1.

RPI in a 50-year-old man with MCA occlusion.

A, DWI showing acute right corona radiata infarction (arrow).

B, MRA shows right MCA occlusion (arrow). Selective ASL of the left ICA circulation (green box), right ICA, and basilar arterial circulations was performed in turn to produce RPI maps (C).

C, Combined RPI map showing the brain tissue perfused by each intracranial artery. The right medial and inferior frontal lobes are supplied by the right ICA (in red), whereas the parietal and inferior temporal lobes are supplied by the basilar artery (in blue). Some areas in the ischemic right MCA territory do not show perfusion by any vascular territory (arrows).

D, X-ray angiogram confirms the posterior cerebral artery pial collateral supply to the right parietal lobe (arrows).

E, SPECT image after acetazolamide challenge shows an area of reduced vascular reserve (arrow) corresponding to the area that does not receive arterial supply from any of the labeled territories (arrows in C).

Discussion

Regional perfusion imaging by using an ASL method developed for 3T MR imaging scanners can provide functional information about both collateral blood supply and brain tissue perfusion. Various brain perfusion imaging techniques have been used to evaluate the hemodynamics in patients with cerebrovascular disease.6–9 The difference (or mismatch) between abnormal areas on DWI and perfusion MR imaging studies may represent the potentially salvageable ischemic tissue at risk of infarction and has been used to target patients for thrombolytic therapy.10 However, the definition of hemodynamically significant arterial stenosis must also take into account the protective effect of collateral circulation, which influences final infarct size and clinical outcomes.1–3 Unfortunately, current methods of assessing collateral circulation by using x-ray angiography are invasive and are typically not performed in patients with acute stroke. A noninvasive method that incorporates functional information into perfusion MR imaging studies to better characterize the role of collaterals in therapeutic and prognostic applications would, therefore, be desirable.1

In the patient we described, RPI could provide functional information about both collateral blood supply and brain tissue perfusion. By exclusively labeling the spins within individual intracranial arteries, we can selectively measure the regions of the brain perfused by each artery, including the territories supplied by collateral circulation.11,12 This process of individual labeling is conceptually similar to x-ray angiography, using a virtual “injection” of magnetically visible contrast material into the individual arteries. When performed in turn for each artery, the perfusion information may be combined into intuitive 3-colored maps, which show at a glance the ischemic territories perfused by collateral blood supply and, in our patients, correlated well with the collaterals depicted on x-ray angiographic studies. Combined with MR angiography, RPI can potentially provide information comparable to x-ray angiography on the extent and nature (whether by primary channels such as the anterior and posterior communicating arteries or secondary pial arteries) of collateral supply to ischemic brain tissue.

MR-based imaging of cerebral perfusion has many advantages as a noninvasive method of assessing the anatomic and functional status of patients with cerebrovascular disease. RPI does not involve ionizing radiation or exogenous contrast media injection and may be combined with DWI and high-resolution conventional MR imaging. A larger comparative study would be useful to help define the potential role of RPI in cerebral ischemia. Neuroimaging techniques such as RPI that can correlate the anatomic with the functional status of regional cerebral perfusion would greatly enhance our understanding of the collateral circulation and potentially supplement or replace x-ray angiography for certain clinical indications.1,13,14

Footnotes

  • This work was supported by NMRC/CPG/009/2004, 0919/2004 and NHGA-RPR/04012 grants.

References

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    Liebeskind DS. Collateral circulation. Stroke 2003;34:2279–84
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  2. Schomer DF, Marks MP, Steinberg GK, et al. The anatomy of the posterior communicating artery as a risk factor for ischemic cerebral infarction. N Engl J Med 1994;330:1565–70
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    Kim JJ, Fischbein NJ, Lu Y, et al. Regional angiographic grading system for collateral flow: correlation with cerebral infarction in patients with middle cerebral artery occlusion. Stroke 2004;35:1340–44
    Abstract/FREE Full Text
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    Latchaw RE, Yonas H, Hunter GJ, et al. Guidelines and recommendations for perfusion imaging in cerebral ischemia: a scientific statement for healthcare professionals by the writing group on perfusion imaging, from the Council on Cardiovascular Radiology of the American Heart Association. Stroke 2003;34:1084–104
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    Golay X, Petersen ET, Hui F. Pulsed star labeling of arterial regions (PULSAR): A robust regional perfusion technique for high-field imaging. Magn Reson Med 2004;53:15–21
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    Powers WJ. Cerebral hemodynamics in ischemic cerebrovascular disease. Ann Neurol 1991;29:231–40
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  7. Wintermark M, Smith WS, Ko NU, et al. Dynamic perfusion CT: optimizing the temporal resolution and contrast volume for calculation of perfusion CT parameters in stroke patients. AJNR Am J Neuroradiol 2004;25:720–29
    Abstract/FREE Full Text
  8. Koh TS, Wu XY, Cheong LH, et al. Assessment of perfusion by dynamic contrast-enhanced imaging using a deconvolution approach based on regression and singular value decomposition. IEEE Trans Med Imaging 2004;23:1532–42
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    Lee CE, Ng HB, Yip CW, et al. Imaging collateral circulation: magnetic resonance angiography and perfusion magnetic resonance imaging at 3 T. Arch Neurol 2005;62:492–93
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    Warach S. Thrombolysis in stroke beyond three hours: targeting patients with diffusion and perfusion MRI. Ann Neurol 2002;51:11–13
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    Golay X, Hendrikse J, Lim TC. Perfusion imaging using arterial spin labeling. Top Magn Reson Imaging 2004;15:10–27
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    Hendrikse J, van der Grond J, Lu H, et al. Flow territory mapping of the cerebral arteries with regional perfusion MRI. Stroke 2004;35:882–87
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    Petersen ET, Lim T, Golay X. Model-free arterial spin-labeling quantification approach for perfusion MRI. Magn Res Med 2006;55:219–32
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    Golay X, Hendrikse J, van der Grond J. Application of regional perfusion imaging to extra-intracranial bypass surgery and severe stenosis. J Neuroradiol 2005;32:321–24
    CrossRefPubMed
  • Received April 5, 2006.
  • Accepted after revision May 1, 2006.
  • Copyright © American Society of Neuroradiology
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C.C.T. Lim, E.T. Petersen, I. Ng, P.Y.K. Hwang, F. Hui, X. Golay
MR Regional Perfusion Imaging: Visualizing Functional Collateral Circulation
American Journal of Neuroradiology Mar 2007, 28 (3) 447-448;

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MR Regional Perfusion Imaging: Visualizing Functional Collateral Circulation
C.C.T. Lim, E.T. Petersen, I. Ng, P.Y.K. Hwang, F. Hui, X. Golay
American Journal of Neuroradiology Mar 2007, 28 (3) 447-448;
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