M Borgmann1,2, M Holtkamp3,4, M Adli1,5, J Behr6,7. 1. Klinik für Psychiatrie und Psychotherapie, Forschungsbereich Experimentelle und Molekulare Psychiatrie, Campus Mitte, Experimentalstandort Dahlem, Charité - Universitätsmedizin Berlin, Garystr. 5, 14195, Berlin, Deutschland. 2. Klinik für Psychiatrie, Psychotherapie und Psychosomatik, Campus Neuruppin, Medizinische Hochschule Brandenburg, 16816, Neuruppin, Deutschland. 3. Klinik für Neurologie, Campus Mitte, Charité - Universitätsmedizin Berlin, 10117, Berlin, Deutschland. 4. Epilepsie-Zentrum Berlin-Brandenburg, Evangelisches Krankenhaus Königin Elisabeth Herzberge, 10365, Berlin, Deutschland. 5. Fliedner Klinik Berlin, 10117, Berlin, Deutschland. 6. Klinik für Psychiatrie und Psychotherapie, Forschungsbereich Experimentelle und Molekulare Psychiatrie, Campus Mitte, Experimentalstandort Dahlem, Charité - Universitätsmedizin Berlin, Garystr. 5, 14195, Berlin, Deutschland. joachim.behr@charite.de. 7. Klinik für Psychiatrie, Psychotherapie und Psychosomatik, Campus Neuruppin, Medizinische Hochschule Brandenburg, 16816, Neuruppin, Deutschland. joachim.behr@charite.de.
Abstract
BACKGROUND: Epilepsy and depressive disorders show a high rate of comorbidity. Thus, neurobiological similarities and a bidirectional relationship in terms of pathogenesis have been suggested. OBJECTIVES: The aim of this article is to present the common neurobiological features of both disorders, to characterize the bidirectional relationship and to provide an overview of therapeutic consequences. MATERIAL AND METHODS: A review of the current literature and evaluation of studies on the topics of depression and epilepsy are presented. RESULTS: Epilepsy and depression share common neurobiological features. In epileptic patients depression should be diagnosed early and reliably as the successful treatment has a great influence on the prognosis, quality of life and suicide risk in these individuals. In therapeutic doses, antidepressive medication with noradrenergic and specific serotonergic antidepressants (NaSSA) or selective serotonin reuptake inhibitors (SSRI) imparts no clinically relevant epileptogenic potential; however, it increases the quality of life and could have anticonvulsant effects in patients with epilepsy. Clomipramine, bupropion and maprotiline, however, should not be administered to patients with epilepsy as they are known to lower the seizure threshold.
BACKGROUND:Epilepsy and depressive disorders show a high rate of comorbidity. Thus, neurobiological similarities and a bidirectional relationship in terms of pathogenesis have been suggested. OBJECTIVES: The aim of this article is to present the common neurobiological features of both disorders, to characterize the bidirectional relationship and to provide an overview of therapeutic consequences. MATERIAL AND METHODS: A review of the current literature and evaluation of studies on the topics of depression and epilepsy are presented. RESULTS:Epilepsy and depression share common neurobiological features. In epilepticpatientsdepression should be diagnosed early and reliably as the successful treatment has a great influence on the prognosis, quality of life and suicide risk in these individuals. In therapeutic doses, antidepressive medication with noradrenergic and specific serotonergic antidepressants (NaSSA) or selective serotonin reuptake inhibitors (SSRI) imparts no clinically relevant epileptogenic potential; however, it increases the quality of life and could have anticonvulsant effects in patients with epilepsy. Clomipramine, bupropion and maprotiline, however, should not be administered to patients with epilepsy as they are known to lower the seizure threshold.
Authors: Elizabeth J Richardson; H Randall Griffith; Roy C Martin; A LeBron Paige; Christopher C Stewart; Jana Jones; Bruce P Hermann; Michael Seidenberg Journal: Epilepsy Behav Date: 2007-01-09 Impact factor: 2.937
Authors: Robert P Kauffman; V Daniel Castracane; Debie L White; Sandra D Baldock; Ron Owens Journal: Gynecol Endocrinol Date: 2005-09 Impact factor: 2.260