Literature DB >> 11498422

Detection of mesial temporal lobe hypoperfusion in patients with temporal lobe epilepsy by use of arterial spin labeled perfusion MR imaging.

R L Wolf1, D C Alsop, I Levy-Reis, P T Meyer, J A Maldjian, J Gonzalez-Atavales, J A French, A Alavi, J A Detre.   

Abstract

BACKGROUND AND
PURPOSE: Interictal hypometabolism has lateralizing value in cases of temporal lobe epilepsy and positive predictive value for seizure-free outcome after surgery to treat epilepsy. Alterations in regional cerebral metabolism can also be inferred from measurements of regional cerebral perfusion. The purpose of this study was to determine the feasibility of detecting cerebral blood flow (CBF) asymmetries in the mesial temporal lobes using continuous arterial spin labeling perfusion MR imaging, which is a noninvasive method for calculating regional CBF.
METHODS: Twelve patients with medically refractory temporal lobe epilepsy who underwent preoperative evaluation for temporal lobectomy and 12 normal control participants were studied retrospectively. Absolute and normalized mesial temporal CBF measurements were compared between the patient and control groups. Lateralization based on a perfusion asymmetry index was compared with metabolic ((18)[F]-fluorodeoxyglucose positron emission tomography) and hippocampal volumetric asymmetry indices and with clinical lateralization.
RESULTS: Mesial temporal CBF was more asymmetric in patients with temporal lobe epilepsy than in normal control participants, although asymmetric mesial temporal CBF was also found in normal participants, with the left side dominant. Ipsilateral mesial temporal CBF was significantly decreased compared with contralateral mesial temporal CBF in patients with temporal lobe epilepsy. Global CBF measurements were significantly decreased in patients compared with control participants. Asymmetry in mesial temporal blood flow in patients persisted after normalization to global CBF. Lateralization using continuous arterial spin labeling perfusion MR imaging asymmetry index significantly correlated with lateralization based on (18)[F]-fluorodeoxyglucose positron emission tomography hypometabolism, hippocampal volumes, and clinical evaluation.
CONCLUSION: Continuous arterial spin labeling perfusion MR imaging can detect interictal asymmetries in mesial temporal lobe perfusion in patients with temporal lobe epilepsy. This technique is readily combined with routine structural assessment and potentially offers an inexpensive and noninvasive means of screening for asymmetries in interictal mesial temporal lobe function.

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Year:  2001        PMID: 11498422      PMCID: PMC7975208     

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  29 in total

1.  Magnetic resonance image-based hippocampal volumetry: correlation with outcome after temporal lobectomy.

Authors:  C R Jack; F W Sharbrough; G D Cascino; K A Hirschorn; P C O'Brien; W R Marsh
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2.  Reduced transit-time sensitivity in noninvasive magnetic resonance imaging of human cerebral blood flow.

Authors:  D C Alsop; J A Detre
Journal:  J Cereb Blood Flow Metab       Date:  1996-11       Impact factor: 6.200

3.  Functional MRI lateralization of memory in temporal lobe epilepsy.

Authors:  J A Detre; L Maccotta; D King; D C Alsop; G Glosser; M D'Esposito; E Zarahn; G K Aguirre; J A French
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4.  Surface cortical cerebral blood flow monitoring and single photon emission computed tomography: prognostic factors for selecting temporal lobectomy candidates.

Authors:  M E Weinand; L P Carter
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5.  Determination of language dominance using functional MRI: a comparison with the Wada test.

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Journal:  Neurology       Date:  1996-04       Impact factor: 9.910

6.  Three-dimensional imaging characteristics of the HEAD PENN-PET scanner.

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7.  Interictal metabolism and blood flow are uncoupled in temporal lobe cortex of patients with complex partial epilepsy.

Authors:  W D Gaillard; S Fazilat; S White; B Malow; S Sato; P Reeves; P Herscovitch; W H Theodore
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8.  Magnetic resonance spectroscopy in temporal lobe epilepsy.

Authors:  A Connelly; G D Jackson; J S Duncan; M D King; D G Gadian
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9.  Proton magnetic resonance spectroscopy in children with temporal lobe epilepsy.

Authors:  J H Cross; A Connelly; G D Jackson; C L Johnson; B G Neville; D G Gadian
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10.  The effect of carbamazepine on cerebral glucose metabolism.

Authors:  W H Theodore; E Bromfield; L Onorati
Journal:  Ann Neurol       Date:  1989-05       Impact factor: 10.422

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  46 in total

1.  Ictal focal hyperperfusion demonstrated by arterial spin-labeling perfusion MRI in partial epilepsy status.

Authors:  Makoto Oishi; Go Ishida; Ken Morii; Kenji Hasegawa; Mitsuya Sato; Yukihiko Fujii
Journal:  Neuroradiology       Date:  2012-03-16       Impact factor: 2.804

2.  Hemodynamic studies of intracranial dural arteriovenous fistulas using arterial spin-labeling MR imaging.

Authors:  T Noguchi; H Irie; Y Takase; M Kawashima; T Ootsuka; M Nishihara; Y Egashira; J Nojiri; T Matsushima; S Kudo
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3.  Arterial spin labeling in neuroimaging.

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4.  Arterial spin labeling at 3.0 Tesla in subacute ischemia: comparison to dynamic susceptibility perfusion.

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5.  Magnetic resonance imaging in 120 patients with intractable partial seizures: a preoperative assessment.

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6.  Measurement of cerebral perfusion with arterial spin labeling: Part 2. Applications.

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Review 7.  Clinical neuroimaging using arterial spin-labeled perfusion magnetic resonance imaging.

Authors:  Ronald L Wolf; John A Detre
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8.  Perfusion imaging of meningioma by using continuous arterial spin-labeling: comparison with dynamic susceptibility-weighted contrast-enhanced MR images and histopathologic features.

Authors:  H Kimura; H Takeuchi; Y Koshimoto; H Arishima; H Uematsu; Y Kawamura; T Kubota; H Itoh
Journal:  AJNR Am J Neuroradiol       Date:  2006-01       Impact factor: 3.825

9.  A qualitative comparison of arterial spin labelling and dynamic susceptibility contrast MRI in 52 children with a range of neurological conditions.

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Review 10.  Shared cognitive and behavioral impairments in epilepsy and Alzheimer's disease and potential underlying mechanisms.

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