Brain, Vol. 123, No. 4, 770-780,
April 2000
© 2000 Oxford University Press
Visual confrontation naming and hippocampal function
A neural network study using quantitative 1H magnetic resonance spectroscopy
Epilepsy Center, Department of Neurology, University of Alabama at Birmingham, USA
Correspondence to:
Stephen M. Sawrie, PhD, UAB Epilepsy Center, 1719 6th Avenue South, CIRC 312, Birmingham, AL 35294 USA E-mail: ssawrie{at}uab.edu
Prior research on the relationship between visual confrontation naming and hippocampal function has been inconclusive. The present study examined this relationship using quantitative 1H magnetic resonance spectroscopy (1H-MRS) to operationalize the function of the left and right hippocampi. The 60-item Boston Naming Test (BNT) was used to measure naming. Our sample included 46 patients with medically intractable, focal mesial temporal lobe epilepsy who had been screened for all pathology other than mesial temporal sclerosis. Statistics included Pearson correlations and neural network analysis (multilayer perceptron and radial basis function). Baseline BNT performance correlated significantly with left 1H-MRS hippocampal ratios. Thirty-six per cent of the variance in baseline BNT performance was explained by a neural network model using left and right 1H-MRS ratios(creatine/N-acetylaspartate) as input. This was elevated to 49% when input from the right hippocampus was lesioned mathematically. In a second model, left 1H-MRS hippocampal ratios were modelled using measures of semantic and episodic memory as input (including the BNT). Explained variance in left 1H-MRS hippocampal ratios fell from 60.8 to 3.6% when input from BNT and another semantic memory measure was degraded mathematically. These results provide evidence that the speech-dominant hippocampus is a significant component of the overall neuroanatomical network of visual confrontation naming. Clinical and theoretical implications are explored.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
A. T.-D. Fonseca, E. Guedj, F-X. Alario, V. Laguitton, O. Mundler, P. Chauvel, and C. Liegeois-Chauvel Brain regions underlying word finding difficulties in temporal lobe epilepsy Brain, October 1, 2009; 132(10): 2772 - 2784. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. A. Josephs, J. L. Whitwell, D. S. Knopman, W. T. Hu, D. A. Stroh, M. Baker, R. Rademakers, B. F. Boeve, J. E. Parisi, G. E. Smith, et al. Abnormal TDP-43 immunoreactivity in AD modifies clinicopathologic and radiologic phenotype Neurology, May 6, 2008; 70(19_Part_2): 1850 - 1857. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Hamberger, W. T. Seidel, R. R. Goodman, A. Williams, K. Perrine, O. Devinsky, and G. M. McKhann II Evidence for cortical reorganization of language in patients with hippocampal sclerosis Brain, November 1, 2007; 130(11): 2942 - 2950. [Abstract] [Full Text] [PDF] |
||||
![]() |
L Bartha, T Benke, G Bauer, and E Trinka Interictal language functions in temporal lobe epilepsy J. Neurol. Neurosurg. Psychiatry, June 1, 2005; 76(6): 808 - 814. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-F. Demonet, G. Thierry, and D. Cardebat Renewal of the Neurophysiology of Language: Functional Neuroimaging Physiol Rev, January 1, 2005; 85(1): 49 - 95. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Kapur and M. D Kopelman Advanced brain imaging procedures and human memory disorder Br. Med. Bull., March 1, 2003; 65(1): 61 - 81. [Abstract] [Full Text] [PDF] |
||||




