Atrophy and cognitive profiles in older adults with temporal lobe epilepsy are similar to mild cognitive impairment

Author:

Kaestner Erik1ORCID,Reyes Anny12,Chen Austin1,Rao Jun1,Macari Anna Christina1,Choi Joon Yul3,Qiu Deqiang4,Hewitt Kelsey5,Wang Zhong Irene3,Drane Daniel L56,Hermann Bruce7,Busch Robyn M3ORCID,Punia Vineet3ORCID,McDonald Carrie R128,

Affiliation:

1. Center for Multimodal Imaging and Genetics, University of California, San Diego, CA, USA

2. San Diego State University/University of California San Diego Joint Doctoral Program in Clinical Psychology, San Diego, CA, USA

3. Epilepsy Center and Department of Neurology, Cleveland Clinic, Cleveland, OH, USA

4. Department of Radiology, Emory University School of Medicine, Atlanta, GA, USA

5. Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA

6. Department of Neurology, University of Washington, Seattle, WA, USA

7. Matthews Neuropsychology Section, University of Wisconsin, Madison, WI, USA

8. Department of Psychiatry, University of California, San Diego, CA, USA

Abstract

Abstract Epilepsy incidence and prevalence peaks in older adults yet systematic studies of brain ageing and cognition in older adults with epilepsy remain limited. Here, we characterize patterns of cortical atrophy and cognitive impairment in 73 older adults with temporal lobe epilepsy (>55 years) and compare these patterns to those observed in 70 healthy controls and 79 patients with amnestic mild cognitive impairment, the prodromal stage of Alzheimer’s disease. Patients with temporal lobe epilepsy were recruited from four tertiary epilepsy surgical centres; amnestic mild cognitive impairment and control subjects were obtained from the Alzheimer’s Disease Neuroimaging Initiative database. Whole brain and region of interest analyses were conducted between patient groups and controls, as well as between temporal lobe epilepsy patients with early-onset (age of onset <50 years) and late-onset (>50 years) seizures. Older adults with temporal lobe epilepsy demonstrated a similar pattern and magnitude of medial temporal lobe atrophy to amnestic mild cognitive impairment. Region of interest analyses revealed pronounced medial temporal lobe thinning in both patient groups in bilateral entorhinal, temporal pole, and fusiform regions (all P < 0.05). Patients with temporal lobe epilepsy demonstrated thinner left entorhinal cortex compared to amnestic mild cognitive impairment (P = 0.02). Patients with late-onset temporal lobe epilepsy had a more consistent pattern of cortical thinning than patients with early-onset epilepsy, demonstrating decreased cortical thickness extending into the bilateral fusiform (both P < 0.01). Both temporal lobe epilepsy and amnestic mild cognitive impairment groups showed significant memory and language impairment relative to healthy control subjects. However, despite similar performances in language and memory encoding, patients with amnestic mild cognitive impairment demonstrated poorer delayed memory performances relative to both early and late-onset temporal lobe epilepsy. Medial temporal lobe atrophy and cognitive impairment overlap between older adults with temporal lobe epilepsy and amnestic mild cognitive impairment highlights the risks of growing old with epilepsy. Concerns regarding accelerated ageing and Alzheimer’s disease co-morbidity in older adults with temporal lobe epilepsy suggests an urgent need for translational research aimed at identifying common mechanisms and/or targeting symptoms shared across a broad neurological disease spectrum.

Funder

National Institute of Health

Alzheimer's Disease Neuroimaging Initiative

National Institutes of Health

Department of Defense award

National Institute on Aging

National Institute of Biomedical Imaging and Bioengineering

AbbVie

Alzheimer’s Association

Alzheimer’s Drug Discovery Foundation

Araclon Biotech

BioClinica, Inc.

NIH

NINDS

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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