کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6273062 1614790 2015 13 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Neuroscience Forefront ReviewSeizures in Alzheimer's disease
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
Neuroscience Forefront ReviewSeizures in Alzheimer's disease
چکیده انگلیسی


- Clinical data from familial and sporadic AD patients reveal increased seizure risk.
- Many APP-linked AD mouse models develop seizures and other EEG abnormalities.
- APP and/or APP-derived peptides may link AD pathology to epileptiform activity.
- Epileptiform activity in AD mouse models can be rescued independent of Aβ reduction.
- Anti-epileptic drugs such as LEV may rescue cognitive dysfunction in AD patients.

Alzheimer's disease (AD) increases the risk for late-onset seizures and neuronal network abnormalities. An elevated co-occurrence of AD and seizures has been established in the more prevalent sporadic form of AD. Recent evidence suggests that nonconvulsive network abnormalities, including seizures and other electroencephalographic abnormalities, may be more commonly found in patients than previously thought. Patients with familial AD are at an even greater risk for seizures, which have been found in patients with mutations in PSEN1, PSEN2, or APP, as well as with APP duplication. This review also provides an overview of seizure and electroencephalography studies in AD mouse models. The amyloid-β (Aβ) peptide has been identified as a possible link between AD and seizures, and while Aβ is known to affect neuronal activity, the full-length amyloid precursor protein (APP) and other APP cleavage products may be important for the development and maintenance of cortical network hyperexcitability. Nonconvulsive epileptiform activity, such as seizures or network abnormalities that are shorter in duration but may occur with higher frequency, may contribute to cognitive impairments characteristic of AD, such as amnestic wandering. Finally, the review discusses recent studies using antiepileptic drugs to rescue cognitive deficits in AD mouse models and human patients. Understanding the mechanistic link between epileptiform activity and AD is a research area of growing interest. Further understanding of the connection between neuronal hyperexcitability and Alzheimer's as well as the potential role of epileptiform activity in the progression of AD will be beneficial for improving treatment strategies.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience - Volume 286, 12 February 2015, Pages 251-263
نویسندگان
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