Abstract
Twelve patients with ICA stenosis underwent dynamic perfusion computed tomography (CT) and positron emission tomography (PET) studies at rest and after acetazolamide challenge. Cerebral blood flow (CBF) maps on perfusion CT resulted from a deconvolution of parenchymal time-concentration curves by an arterial input function (AIF) in the anterior cerebral artery as well as in both anterior choroidal arteries. CBF was measured by [15O]H2O PET using multilinear least-squares minimization procedure based on the one-compartment model. In corresponding transaxial PET scans, CBF values were extracted using standardized ROIs. The baseline perfusion CT-CBF values were lower in perfusion CT than in PET (P>0.05). CBF values obtained by perfusion CT were significantly correlated with those measured by PET before (P<0.05) and after (P<0.01) acetazolamide challenge. Nevertheless, the cerebrovascular reserve capacity was overestimated (P=0.05) using perfusion CT measurements. The AIF selection relative to the side of carotid stenosis did not significantly affect calculated perfusion CT-CBF values. In conclusion, the perfusion CT-CBF measurements correlate significantly with the PET-CBF measurements in chronic carotid stenotic disease and contribute useful information to the evaluation of the altered cerebral hemodynamics.
Similar content being viewed by others
References
Derdeyn CP, Grubb RL Jr, Powers WJ (1999) Cerebral hemodynamic impairment: methods of measurement and association with stroke risk. Neurology 53:251–259
Ringelstein EB, Weiller C, Weckesser M, Weckesser S (1994) Cerebral vasomotor reactivity is significantly reduced in low-flow as compared to thromboembolic infarctions: the key role of the circle of Willis. J Neurol Sci 121:103–109
Hirano T, Minematsu K, Hasegawa Y, Tanaka Y, Hayashida K, Yamaguchi T (1994) Acetazolamide reactivity on 121 I-IMP single photon emission computed tomography in patients with major cerebral artery occlusive disease: correlation with positron emission tomography parameters. J Cereb Blood Flow Metab 16:763–770
Knop J, Thie A, Fuchs C, Siepmann G, Zeumer H (1992) 99mTc-HMPAO-SPECT with acetazolamide challenge to detect hemodynamic compromise in occlusive cerebrovascular disease. Stroke 223:1733–1742
Bickler PE, Litt L, Banville DL, Severinghaus JW (1988) Effects of acetazolamide on cerebral acid-base balance. J Appl Physiol 422–427
Nabavi DG, Cenic A, Craen RA, Gelb AW, Bennett JD, Kozak R, Lee TY (1999) CT assessment of cerebral perfusion: experimental validation and initial clinical experience. Radiology 213:141–149
Calamante F, Gadian DG, Connelly A (2000) Delay and dispersion effects in dynamic susceptibility contrast MRI: simulations using singular value decomposition. Magn Reson Med 44:466–473
Neumann-Haefelin T, Wittsack HJ, Fink GR et al (2000) Diffusion- and perfusion-weighted MRI: influence of severe carotid artery stenosis on the DWI/PWI mismatch in acute stroke. Stroke 31:1311–1317
Yamada K, Wu O, Gonzalez RG et al (2002) Magnetic resonance perfusion-weighted imaging of acute cerebral infarction: effect of the calculation methods and underlying vasculopathy. Stroke 33:87–94
Holl K, Nemati NM, Haubitz B, Mejewski A, Gaab MR, Becker H, Dietz H (1992) Xenon-CT und Bestimmung der zerebrovaskulären Reserve mit Acetazolamid (Diamox) In: Becker H, Gaab MR (eds) Hirndurchblutung und zerebrovaskuläre Reservekapazität. Urban & Schwarzenberg, München
Matzke KH, Meyer GJ, Hundeshagen H (1993) An advanced system for the administration of 15O-water. J Labelled Compd Radiopharm 32:459–460
Van den Hoff J, Burchert M, Müller-Schauenburg W, Meyer GJ, Hundeshagen H (1993) Accurate local blood flow measurement with dynamic PET: fast determination of input function delay and dispersion by multilinear minimization. J Nucl Med 34:1770–1777
Talairach J, Tournoux P (1988) Co-planar stereotaxic atlas of the human brain. Thieme, Stuttgart
Gillard JH, Minhas PS, Hayball MP et al (2000) Assessment of quantitative computed tomographic cerebral perfusion imaging with H2 15O positron emission tomography. Neurol Res 22:457–464
Huisman TA, Sorensen AG (2004) Perfusion-weighted magnetic resonance imaging of the brain: techniques and application in children. Eur Radiol 14:59–72
Uematsu H, Maeda M (2006) Double-echo perfusion-weighted MR imaging: basic concepts and application in brain tumors for the assessment of tumor blood volume and vascular-permeability. Eur Radiol 16:180–186
Kudo K, Terae S, Katoh C, Oka M, Shiga T, Tamaki N, Miyasaka K (2003) Quantitative cerebral flow measurement with dynamic perfusion CT using the vascular-pixel elimination method: comparison with H2 15O positron emission tomography. AJNR Am J Neuroradiol 24:419–426
Yamamuchi H, Fukuyama H, Nagahama Y, Katsumi Y, Okazawa H (1998) Cerebral hematocrit decreases with hemodynamic compromise in carotid artery occlusion: a PET study. Stroke 29:98–103
Eastwood JD, Lev MH, Azhari T et al (2002) CT perfusion scanning with deconvolution analysis: pilot study in patients with acute middle cerebral artery stroke. Radiology 222:227–236
Bisdas S, Donnerstag F, Ahl B, Bohrer I, Weissenborn K, Becker H (2004) Comparison of perfusion computed tomography with diffusion-weighted magnetic resonance imaging in hyperacute ischemic stroke. J Comput Assist Tomogr 28:747–755
Lythgoe DJ, Østergaard L, Williams SCR, Cluckie A, Buxton-Thomas M, Simmons A, Markus HS (2000) Quantitative perfusion imaging in carotid artery stenosis using dynamic susceptibility contrast-enhanced magnetic resonance imaging. Magn Reson Imaging 18:1–11
Østergaard L, Sorensen AG, Kwong KK, Weisskoff RM, Gyldensted C, Rosen BR (1996) High resolution measurement of cerebral blood flow using intavascular tracer bolus passages, II: experimental comparison and preliminary results. Magn Reson Med 36:726–736
Axel L (1980) Cerebral blood flow determination by rapid-sequence computed tomography: a theoretical analysis. Radiology 137:679–686
Hofmeijer J, Klijn CMJ, Kappelle LJ, van Huffelen AC, van Gijn J (2002) Collateral circulation via the ophthalmic artery or leptomeningeal vessels is associated with impaired cerebral vasoreactivity in patients with symptomatic carotid artery occlusion. Cerebrovasc Dis 14:22–26
Ozgur HT, Kent Walsh T, Masaryk A et al (2001) Correlation of cerebrovascular reserve as measured by acetazolamide-challenged SPECT with angiographic flow patterns and intra- or extracranial arterial stenosis. AJNR Am J Neuroradiol 22:928–936
Kikuchi K, Murase K, Miki H, Kikuchi T, Sugawara Y, Mochizuki T, Ikezoe J, Ohue S (2001) Measurement of cerebral hemodynamics with perfusion-weighted MR imaging: comparison with pre- and post-acetazolamide 133Xe-SPECT in occlusive carotid disease. AJNR Am J Neuroradiol 22:248–254
Greitz T (1956) A radiologic study of the brain circulation by rapid serial angiography of the carotid artery. Acta Radiol Suppl 140:1–123
Yamamoto S, Watanabe M, Uematsu T, Takasawa K, Nukata M, Kinoshita N (2004) Correlation of angiographic circulation time and cerebrovascular reserve by acetazolamide-challenged single photon emission CT. AJNR Am J Neuroradiol 25:242–247
Dahl A, Russell D, Nyberg-Hansen R, Rootwelt K, Mowinckel P (1994) Simultaneous assessment of vasoreactivity using transcranial Doppler ultrasound and cerebral blood flow in healthy subjects. J Cereb Blood Flow Metab 14:974–981
Karnik R, Valentin A, Winkler WB, Khaffaf N, Donath P, Slany J (1996) Sex-related differences in acetazolamide-induced cerebral vasomotor reactivity. Stroke 27:56–58
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Bisdas, S., Nemitz, O., Berding, G. et al. Correlative assessment of cerebral blood flow obtained with perfusion CT and positron emission tomography in symptomatic stenotic carotid disease. Eur Radiol 16, 2220–2228 (2006). https://doi.org/10.1007/s00330-006-0209-2
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00330-006-0209-2