Purpose: Previous studies have shown that structural integrity (i.e., presence/absence of mesial temporal sclerosis (MTS)) of the left mesial temporal lobe is associated with verbal memory outcome following left anterior temporal lobectomy (ATL). However, the functional integrity of the left temporal lobe, as exemplified by preoperative verbal memory performance, has also been associated with verbal memory outcome following surgery. We investigated the risk of verbal memory loss in patients with known structural abnormality (i.e., left mesial temporal sclerosis by MRI) and normal preoperative verbal memory performance who undergo left ATL. Methods: Seventeen patients with left temporal lobe epilepsy, MRI-based exclusive left NITS, and normal preoperative verbal memory were identified. Normal verbal memory was defined as performance on both Acquisition (learning across trials 1-5) and Retrieval (long delayed free recall) portions of the California Verbal Learning Test (CVLT) above a T score of 40 (>= 16%ile). Postoperative verbal memory outcome was established by incorporating standardized regression-based (SRB) change scores. Results: Postoperative declines across both CVLT Retrieval T scores and Acquisition T scores (average 20% and average 15% declines from baseline scores, respectively) were measured for the group. The average CVLT Retrieval SRB change score was -2.5, and the average CVLT Acquisition SRB change score was -1.0. A larger proportion of patients demonstrated postoperative declines on Retrieval scores than Acquisition scores (64.7% vs 17.6%, respectively). Conclusions: Even in the presence of left NITS, patients exhibiting normal presurgical verbal memory are at risk for verbal memory declines following ATL. These results suggest that the functional integrity of the left mesial temporal lobe may play an important role in the verbal memory outcome in this patient group. (c) 2005 Elsevier Inc. All rights reserved.
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Univ Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USAUniv Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USA
Mueller, Susanne G.
Laxer, Kenneth D.
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Calif Pacific Med Ctr, Pacific Epilepsy Program, San Francisco, CA USAUniv Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USA
Laxer, Kenneth D.
Scanlon, Cathy
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Univ Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USAUniv Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USA
Scanlon, Cathy
Garcia, Paul
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Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94121 USAUniv Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USA
Garcia, Paul
McMullen, William J.
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Calif Pacific Med Ctr, Pacific Epilepsy Program, San Francisco, CA USAUniv Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USA
McMullen, William J.
Loring, David W.
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Emory Univ, Dept Neurol, Atlanta, GA 30322 USAUniv Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USA
Loring, David W.
Meador, Kimford J.
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Emory Univ, Dept Neurol, Atlanta, GA 30322 USAUniv Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USA
Meador, Kimford J.
Weiner, Michael W.
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Univ Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USAUniv Calif San Francisco, Dept Radiol, Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs DVA Med Ctr, San Francisco, CA 94121 USA