Subclinical epileptiform process in patients with unipolar depression and its indirect psychophysiological manifestations

. 2011 ; 6 (11) : e28041. [epub] 20111122

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid22132204

BACKGROUND: According to recent clinical findings epileptiform activity in temporolimbic structures may cause depressive and other psychiatric symptoms that may occur independently of any seizure in patient's history. In addition in these patients subclinical seizure-like activity with indirect clinical manifestations likely may occur in a form of various forms of cognitive, affective, memory, sensory, behavioral and somatic symptoms (the so-called complex partial seizure-like symptoms). A typical characteristic of epileptiform changes is increased neural synchrony related to spreading of epileptiform activity between hemispheres even in subclinical conditions i.e. without seizures. These findings suggest a hypothesis that measures reflecting a level of synchronization and information transfer between hemispheres could reflect spreading of epileptiform activity and might be related to complex partial seizure-like symptoms. METHODS AND FINDINGS: Suitable data for such analysis may provide various physiological signals reflecting brain laterality, as for example bilateral electrodermal activity (EDA) that is closely related to limbic modulation influences. With this purpose we have performed measurement and analysis of bilateral EDA and compared the results with psychometric measures of complex partial seizure-like symptoms, depression and actually experienced stress in 44 patients with unipolar depression and 35 healthy controls. The results in unipolar depressive patients show that during rest conditions the patients with higher level of complex partial seizure like symptoms (CPSI) display increased level of EDA transinformation (PTI) calculated between left and right EDA records (Spearman correlation between CPSI and PTI is r = 0.43, p = 0.004). CONCLUSIONS: The result may present potentially useful clinical finding suggesting that increased EDA transinformation (PTI) could indirectly indicate increased neural synchrony as a possible indicator of epileptiform activity in unipolar depressive patients treated by serotoninergic antidepresants.

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Kraus JE. Sensitization phenomena in psychiatric illness: lessons from the kindling model. J Neuropsychiatry Clin Neurosci. 2000;12:328–343. PubMed

Roberts RJ, Gorman LL, Lee GP, Hines ME, Richardson ED, et al. The phenomenology of multiple partial seizure-like symptoms without stereotyped spells: an epilepsy spectrum disorder? Epilepsy Res. 1992;13:167–177. PubMed

Silberman EK, Post RM, Nurnberger J, Theodore W, Boulenger JP. Transient sensory, cognitive and affective phenomena in affective illness. A comparison with complex partial epilepsy. Br J Psychiatry. 1985;146:81–89. PubMed

Teicher MH, Andersen SL, Polcari A, Anderson CM, Navalta CP, et al. The neurobiological consequences of early stress and childhood maltreatment. Neurosci Biobehav Rev. 2003;27:33–44. PubMed

Varney NR, Garvey MJ, Cook BL, Campbell DA, Roberts RJ. Identification of treatment-resistant depressives who respond favorably to carbamazepine. Ann Clin Psychiatry. 1993;5:117–122. PubMed

Bob P. Dissociation and neuroscience: history and new perspectives. Int J Neurosci. 2003;113:903–914. PubMed

Bob P. Dissociation and neurobiological consequences of traumatic stress. Activ Nerv Super. 2008;50:9–14.

Johannessen LC. Antiepileptic drugs in non-epilepsy disorders: relations between mechanisms of action and clinical efficacy. CNS Drugs. 2008;22:27–47. PubMed

Post RM, Weiss SR, Pert A. Implications of behavioral sensitization and kindling for stress-induced behavioral change. Adv Exp Med Biol. 1988;245:441–463. PubMed

Post RM. Transduction of psychosocial stress into the neurobiology of recurrent affective disorder. Am J Psychiatry. 1992;149:999–1010. PubMed

Keller MB. Past, present, and future directions for defining optimal treatment outcome in depression: remission and beyond. JAMA. 2003;289:3152–3160. PubMed

Monroe SM, Harkness KL. Life stress, the “kindling” hypothesis, and the recurrence of depression: considerations from a life stress perspective. Psychol Rev. 2005;112:417–445. PubMed

Bob P, Palus M, Susta M, Glaslova K. Sensitization, epileptic-like symptoms and local synchronization in patients with paranoid schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry. 2010;34:143–6. PubMed

Bob P, Susta M, Gregusova A, Jasova D, Mishara A, et al. Traumatic stress, dissociation, and limbic irritability in patients with unipolar depression being treated with SSRIs. Psychol Rep. 2010;107:685–96. PubMed

McIntyre DC, Gilby KL. Mapping seizure pathways in the temporal lobe. Epilepsia. 2008;49(Suppl 3):23–30. PubMed

Roca V, Freeman TW. Psychosensory symptoms in combat veterans with posttraumatic stress disorder. J Neuropsychiatry Clin Neurosci. 2002;14:185–9. PubMed

Weinand ME, Labiner DM, Ahern GL. Temporal lobe seizure interhemispheric propagation time depends on non-epileptic cortical cerebral blood flow. Epilepsy Res. 2001;44:33–39. PubMed

Weinand ME, Hussain N, Labiner DM, Ahern GL. Correlation of electrocorticographic to clinical seizure onset and interhemispheric propagation times in temporal lobe epilepsy. Pathophysiology. 2006;13:233–6. PubMed

Baumgartner C, Lurge RS, Leutmezer F. Autonomic symptoms during epileptic seizures. Epileptic Disord. 2001;3:103–116. PubMed

Devinsky O. Effects of seizures on autonomic and cardiovascular function. Epilepsy Curr. 2004;4:43–46. PubMed PMC

Mangina CA, Beuzeron-Mangina JH. Direct electrical stimulation of specific human brain structures and bilateral electrodermal activity. Int J Psychophysiol. 1996;22:1–8. PubMed

Phelps EA, O'Connor KJ, Gatenby JC, Gore JC, Grillon C, et al. Activation of the left amygdala to a cognitive representation of fear. Nat Neurosci. 2001;4:437–441. PubMed

Critchley HD. Electrodermal Responses: What Happens in the Brain. Neuroscientist. 2002;8:132–142. PubMed

Furmark T, Fischer H, Wik G, Larsson M, Fredrikson M. The amygdala and individual differences in human fear conditioning. Neuroreport. 1997;8:3957–60. PubMed

Poh MZ, Loddenkemper T, Swenson NC, Goyal S, Madsen JR, et al. Continuous monitoring of electrodermal activity during epileptic seizures using a wearable sensor. Conf Proc IEEE Eng Med Biol Soc. 2010:4415–8. PubMed

American Psychiatric Association. American Psychiatric Association, DSM IV, Diagnostic and Statistical Manual of Mental Disorders. 1994. ed 14, Washington DC, American Psychiatric Association.

Sheehan DV, Lecrubier Y, Sheehan KH, Amorim P, Janavs J, et al. The Mini-International Neuropsychiatric Interview (M.I.N.I.): The development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry. 1998;59:22–33. PubMed

Beck AT, Steer RA. Beck Depression Inventory Manual. Psychological Corporation, San Antonio, TX; 1996.

Horowitz M, Wilner M, Alvarez W. Impact of Event Scale: A Measure of Subjective Stress. Psychosom Med. 1979;41:209–218. PubMed

Kantz H, Schreiber T. Nonlinear time series analysis. Cambridge: Cambridge University Press; 1997.

Lambertz M, Vandenhouten R, Grebe R, Langhorst P. Phase transitions in the common brainstem and related systems investigated by nonstationary time series analysis. J Auton Nerv Syst. 2000;78:141–57. PubMed

Bob P, Jasova D, Bizik G, Raboch J. Epileptiform activity in alcohol dependent patients and possibilities of its indirect measurement. PLoS One. 2011;6(4):e18678. PubMed PMC

Caldji C, Diorio J, Meaney MJ. Variations in maternal care alter GABAA receptor subunit expression in brain regions associated with fear. Neuropsychopharmacology. 2003;28:1950–1959. PubMed

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