Ischemic Stroke: Effects of Etiology and Patient Age on the Time Course of the Core Apparent Diffusion Coefficient

PURPOSE: To determine whether the evolution of the core apparent diffusion coefficient (ADC) of water in ischemic stroke varies with patient age or infarct etiology.

MATERIALS AND METHODS: One hundred forty-seven patients with stroke underwent 236 diffusion-weighted magnetic resonance imaging examinations. Etiologies of lesions were classified according to predefined criteria; in 224 images, the diagnosis of lacune could be firmly established or excluded. ADC was measured in the center of each lesion and in contralateral normal-appearing brain. A model was used to describe the time course of relative ADC (rADC), which is calculated by dividing the lesion ADC by the contralateral ADC, and to test for age- or etiology-related differences in this time course.

RESULTS: Transition from decreasing to increasing rADC was estimated at 18.5 hours after stroke onset. In subgroup analysis, transition was earlier in nonlacunes than in lacunes (P = .02). There was a trend toward earlier transition in patients older than the median age of 66.0 years, compared with younger patients (P = .06). Pseudonormalization was estimated at 216 hours. Among nonlacunes, the rate of subsequent rADC increase was more rapid in younger patients than in older patients (P = .001). Within the smaller sample of lacunes, however, no significant age-related difference in this rate was found.

CONCLUSION: Differences in ADC depending on the patient’s age and infarct etiology suggest differing rates of ADC progression.

References

  • 1 Lövblad KO, Laubach HJ, Baird AE, et al. Clinical experience with diffusion-weighted MR in patients with acute stroke. AJNR Am J Neuroradiol 1998; 19:1061-1066. MedlineGoogle Scholar
  • 2 Singer MB, Chong J, Lu D, Schonewille WJ, Tuhrim S, Atlas SW. Diffusion-weighted MRI in acute subcortical infarction. Stroke 1998; 29:133-136. Crossref, MedlineGoogle Scholar
  • 3 Gonzalez RG, Schaefer PW, Buonanno FS, et al. Diffusion-weighted MR imaging: diagnostic accuracy in patients imaged within 6 hours of stroke symptom onset. Radiology 1999; 210:155-162. LinkGoogle Scholar
  • 4 Moseley ME, Kucharczyk J, Mintorovitch J, et al. Diffusion-weighted MR imaging of acute stroke: correlation with T2-weighted and magnetic susceptibility-enhanced MR imaging in cats. AJNR Am J Neuroradiol 1990; 11:423-429. MedlineGoogle Scholar
  • 5 Moseley ME, Cohen Y, Mintorovitch J, et al. Early detection of regional cerebral ischemia in cats: comparison of diffusion- and T2-weighted MRI and spectroscopy. Magn Reson Med 1990; 14:330-346. Crossref, MedlineGoogle Scholar
  • 6 Davis D, Ulatowski J, Eleff S, et al. Rapid monitoring of changes in water diffusion coefficients during reversible ischemia in cat and rat brain. Magn Reson Med 1994; 31:454-460. Crossref, MedlineGoogle Scholar
  • 7 Pierpaoli C, Alger JR, Righini A, et al. High temporal resolution diffusion MRI of global cerebral ischemia and reperfusion. J Cereb Blood Flow Metab 1996; 16:892-905. Crossref, MedlineGoogle Scholar
  • 8 Yoneda Y, Tokui K, Hanihara T, Kitagaki H, Tabuchi M, Mori E. Diffusion-weighted magnetic resonance imaging: detection of ischemic injury 39 minutes after onset in a stroke patient. Ann Neurol 1999; 45:794-797. Crossref, MedlineGoogle Scholar
  • 9 Warach S, Chien D, Li W, Ronthal M, Edelman RR. Fast magnetic resonance diffusion-weighted imaging of acute human stroke. Neurology 1992; 42:1717-1723. Crossref, MedlineGoogle Scholar
  • 10 Warach S, Gaa J, Siewert B, Wielopolski P, Edelman RR. Acute human stroke studied by whole brain echo planar diffusion-weighted magnetic resonance imaging. Ann Neurol 1995; 37:231-241. Crossref, MedlineGoogle Scholar
  • 11 Lutsep HL, Albers GW, DeCrespigny A, Kamat GN, Marks MP, Moseley ME. Clinical utility of diffusion-weighted magnetic resonance imaging in the assessment of ischemic stroke. Ann Neurol 1997; 41:574-580. Crossref, MedlineGoogle Scholar
  • 12 Schlaug G, Siewert B, Benfield A, Edelman RR, Warach S. Time course of the apparent diffusion coefficient (ADC) abnormality in human stroke. Neurology 1997; 49:113-119. Crossref, MedlineGoogle Scholar
  • 13 Nagesh V, Welch KM, Windham JP, et al. Time course of ADCw changes in ischemic stroke: beyond the human eye. Stroke 1998; 29:1778-1782. Crossref, MedlineGoogle Scholar
  • 14 Schwamm LH, Koroshetz WJ, Sorensen AG, et al. Time course of lesion development in patients with acute stroke: serial diffusion- and hemodynamic-weighted magnetic resonance imaging. Stroke 1998; 29:2268-2276. Crossref, MedlineGoogle Scholar
  • 15 Yang Q, Tress BM, Barber PA, et al. Serial study of apparent diffusion coefficient and anisotropy in patients with acute stroke. Stroke 1999; 30:2382-2390. Crossref, MedlineGoogle Scholar
  • 16 Beaulieu C, de Crespigny A, Tong DC, Moseley ME, Albers GW, Marks MP. Longitudinal magnetic resonance imaging study of perfusion and diffusion in stroke: evolution of lesion volume and correlation with clinical outcome. Ann Neurol 1999; 46:568-578. Crossref, MedlineGoogle Scholar
  • 17 Hossmann KA. Cortical steady potential, impedance and excitability changes during and after total ischemia of cat brain. Exp Neurol 1971; 32:163-175. Crossref, MedlineGoogle Scholar
  • 18 Benveniste H, Hedlund LW, Johnson GA. Mechanism of detection of acute cerebral ischemia in rats by diffusion-weighted magnetic resonance microscopy. Stroke 1992; 23:746-754. Crossref, MedlineGoogle Scholar
  • 19 Siesjö BK. Pathophysiology and treatment of focal cerebral ischemia. I. Pathophysiology. J Neurosurg 1992; 77:169-184. Google Scholar
  • 20 Szafer A, Zhong J, Gore JC. Theoretical model for water diffusion in tissues. Magn Reson Med 1995; 33:697-712. Crossref, MedlineGoogle Scholar
  • 21 Anderson AW, Zhong J, Petroff OA, et al. Effects of osmotically driven cell volume changes on diffusion-weighted imaging of the rat optic nerve. Magn Reson Med 1996; 35:162-167. Crossref, MedlineGoogle Scholar
  • 22 van der Toorn A, Sykova E, Dijkhuizen RM, et al. Dynamic changes in water ADC, energy metabolism, extracellular space volume, and tortuosity in neonatal rat brain during global ischemia. Magn Reson Med 1996; 36:52-60. Crossref, MedlineGoogle Scholar
  • 23 Dijkhuizen RM, de Graaf RA, Tulleken KA, Nicolay K. Changes in the diffusion of water and intracellular metabolites after excitotoxic injury and global ischemia in neonatal rat brain. J Cereb Blood Flow Metab 1999; 19:341-349. Crossref, MedlineGoogle Scholar
  • 24 Neil JJ, Duong TQ, Ackerman JJ. Evaluation of intracellular diffusion in normal and globally-ischemic rat brain via 133Cs NMR. Magn Reson Med 1996; 35:329-335. Crossref, MedlineGoogle Scholar
  • 25 Duong TQ, Ackerman JJ, Ying HS, Neil JJ. Evaluation of extra- and intracellular apparent diffusion in normal and globally ischemic rat brain via 19F NMR. Magn Reson Med 1998; 40:1-13. Crossref, MedlineGoogle Scholar
  • 26 Helpern JA, Ordidge RJ, Knight RA. The effect of cell membrane water permeability on the apparent diffusion coefficient of water (abstr) In: Book of abstracts: Society of Magnetic Resonance in Medicine 1992. Berkeley, Calif: Society of Magnetic Resonance in Medicine, 1992; 1201. Google Scholar
  • 27 Takahashi M, Fritz-Zieroth B, Chikugo T, Ogawa H. Differentiation of chronic lesions after stroke in stroke-prone spontaneously hypertensive rats using diffusion weighted MRI. Magn Reson Med 1993; 30:485-488. Crossref, MedlineGoogle Scholar
  • 28 Welch KM, Windham J, Knight RA, et al. A model to predict the histopathology of human stroke using diffusion and T2-weighted magnetic resonance imaging. Stroke 1995; 26:1983-1989. Crossref, MedlineGoogle Scholar
  • 29 Matsumoto K, Lo EH, Pierce AR, Wei H, Garrido L, Kowall NW. Role of vasogenic edema and tissue cavitation in ischemic evolution on diffusion-weighted imaging: comparison with multiparameter MR and immunohistochemistry. AJNR Am J Neuroradiol 1995; 16:1107-1115. MedlineGoogle Scholar
  • 30 Jiang Q, Zhang ZG, Chopp M, et al. Temporal evolution and spatial distribution of the diffusion constant of water in rat brain after transient middle cerebral artery occlusion. J Neurol Sci 1993; 120:123-130. Crossref, MedlineGoogle Scholar
  • 31 Helpern JA, Dereski MO, Knight RA, Ordidge RJ, Chopp M, Qing ZX. Histopathological correlations of nuclear magnetic resonance imaging parameters in experimental cerebral ischemia. Magn Reson Imaging 1993; 11:241-246. Crossref, MedlineGoogle Scholar
  • 32 Knight RA, Dereski MO, Helpern JA, Ordidge RJ, Chopp M. Magnetic resonance imaging assessment of evolving focal cerebral ischemia: comparison with histopathology in rats. Stroke 1994; 25:1252-1261. Crossref, MedlineGoogle Scholar
  • 33 Clavier I, Hommel M, Besson G, Noelle B, Perret JE. Long-term prognosis of symptomatic lacunar infarcts: a hospital-based study. Stroke 1994; 25:2005-2009. Crossref, MedlineGoogle Scholar
  • 34 Adams HP, Jr, Davis PH, Leira EC, et al. Baseline NIH Stroke Scale score strongly predicts outcome after stroke: a report of the Trial of Org 10172 in Acute Stroke Treatment (TOAST). Neurology 1999; 53:126-131. Crossref, MedlineGoogle Scholar
  • 35 Nakayama H, Jorgensen HS, Raaschou HO, Olsen TS. The influence of age on stroke outcome: the Copenhagen stroke study. Stroke 1994; 25:808-813. Crossref, MedlineGoogle Scholar
  • 36 Jorgensen HS, Reith J, Nakayama H, Kammersgaard LP, Raaschou HO, Olsen TS. What determines good recovery in patients with the most severe strokes? the Copenhagen stroke study. Stroke 1999; 30:2008-2012. Crossref, MedlineGoogle Scholar
  • 37 Adams HP, Jr, Bendixen BH, Kappelle LJ, et al. Classification of subtype of acute ischemic stroke: definitions for use in a multicenter clinical trial—TOAST: Trial of ORG 10172 in Acute Stroke Treatment. Stroke 1993; 24:35-41. Crossref, MedlineGoogle Scholar
  • 38 Stejskal E, Tanner J. Spin diffusion measurements: spin echoes in the presence of a time-dependent field gradient. J Chem Phys 1965; 42:288-292. CrossrefGoogle Scholar
  • 39 Kidwell CS, Saver JL, Mattiello J, et al. Thrombolytic reversal of acute human cerebral ischemic injury shown by diffusion/perfusion magnetic resonance imaging. Ann Neurol 2000; 47:462-469. Crossref, MedlineGoogle Scholar
  • 40 Sorensen AG, Buonanno FS, Gonzalez RG, et al. Hyperacute stroke: evaluation with combined multisection diffusion-weighted and hemodynamically weighted echo-planar MR imaging. Radiology 1996; 199:391-401. LinkGoogle Scholar
  • 41 Baird AE, Benfield A, Schlaug G, et al. Enlargement of human cerebral ischemic lesion volumes measured by diffusion-weighted magnetic resonance imaging. Ann Neurol 1997; 41:581-589. Crossref, MedlineGoogle Scholar
  • 42 Barber PA, Darby DG, Desmond PM, et al. Prediction of stroke outcome with echoplanar perfusion- and diffusion-weighted MRI. Neurology 1998; 51:418-426. Crossref, MedlineGoogle Scholar
  • 43 van Everdingen KJ, van der Grond J, Kappelle LJ, Ramos LM, Mali WP. Diffusion-weighted magnetic resonance imaging in acute stroke. Stroke 1998; 29:1783-1790. Crossref, MedlineGoogle Scholar
  • 44 Sorensen AG, Copen WA, Østergaard L, et al. Hyperacute stroke: simultaneous measurement of relative cerebral blood volume, relative cerebral blood flow, and mean tissue transit time. Radiology 1999; 210:519-527. LinkGoogle Scholar

Article History

Published in print: Oct 2001